US20230103401A1

US20230103401A1 - Pharmaceutical composition comprising bispecific antibody constructs

Info

Publication number: US20230103401A1
Application number: US17/854,891
Authority: US
Inventors: Sekhar Kanapuram; Ramil Latypov; Balakumar Thangaraj; Cornelius Pompe
Original assignee: Amgen Research Munich GmbH; Amgen Inc
Current assignee: Amgen Research Munich GmbH; Amgen Inc
Priority date: 2016-01-25
Filing date: 2022-06-30
Publication date: 2023-04-06
Also published as: BR112018014986A2; UA126279C2; ZA201804354B; AU2017213050B2; US11419933B2; AR107444A1; SG11201805738QA; IL260753B1; HUE063319T2; IL260753B2; FI3408295T3; PH12018501419A1; PL3408295T3; MX2018009060A; JP7168451B2; IL260753A; TW201728339A; CN109071657A; JOP20170017B1; TN2018000260A1

Abstract

The present invention provides novel and stable pharmaceutical compositions comprising bispecific single chain antibody constructs, cyclodextrins and a buffer.

Description

BACKGROUND

The advent of recombinant DNA technology has allowed the development of many protein pharmaceuticals in the past three decades. Protein-based pharmaceuticals are now among the fastest growing categories of therapeutic agents in (pre)clinical development and as commercial products. In comparison with small chemical drugs, protein pharmaceuticals have high specificity and activity at relatively low concentrations, and typically provide for therapy of high impact diseases such as various cancers, auto-immune diseases, and metabolic disorders (Roberts, Trends Biotechnol. 2014 July; 32(7):372-80, Wang, Int J Pharm. 1999 Aug. 20; 185(2):129-88).
Due to advances in commercial scale purification processes, recombinant proteins can now be obtained in high purity when first manufactured. However, proteins are only marginally stable and are highly susceptible to degradation, both chemical and physical. Chemical degradation refers to modifications involving covalent bonds, such as deamidation, oxidation, cleavage or formation of new disulfide bridges, hydrolysis, isomerization, or deglycosylation. Physical degradation includes protein unfolding, undesirable adsorption to surfaces, and aggregation. Dealing with these physical and chemical instabilities is one of the most challenging tasks in the development of protein pharmaceuticals (Chi et al., Pharm Res, Vol. 20, No. 9, September 2003, pp. 1325-1336, Roberts, Trends Biotechnol. 2014 July; 32(7):372-80).
Protein aggregation represents a major event of physical instability of proteins and occurs due to the inherent tendency to minimize the thermodynamically unfavorable interaction between the solvent and hydrophobic protein residues. It is particularly problematic because it is encountered routinely during refolding, purification, sterilization, shipping, and storage processes. Aggregation can occur even under solution conditions where the protein native state is highly thermodynamically favored (e.g., neutral pH and 37° C.) and in the absence of stresses (Chi et al., Pharm Res, Vol. 20, No. 9, September 2003, pp. 1325-1336, Roberts, Trends Biotechnol. 2014 July; 32(7):372-80, Wang, Int J Pharm. 1999 Aug. 20; 185(2):129-88, Mahler J Pharm Sci. 2009 September; 98(9):2909-34.).
Protein aggregation is problematic because it can impair biological activity of the therapeutic proteins. Moreover, aggregation of proteins leads to undesirable aesthetics of the drug product, and decreases product yield due to elaborate purification steps that are required to remove the aggregates from the end product. More recently, there has also been growing concern and evidence that the presence of aggregated proteins (even humanized or fully human proteins) can significantly increase the risk that a patient will develop an immune response to the active protein monomer, resulting in the formation of neutralizing antibodies and drug resistance, or other adverse side effects (Mahler J Pharm Sci. 2009 September; 98(9):2909-34.
Several efforts have been reported in the literature to minimize protein aggregation by various mechanisms. Proteins can be stabilized and thus protected from aggregate formation and other chemical changes by modifying their primary structure, thereby increasing interior hydrophobicity and reducing outer hydrophobicity. However, genetic engineering of proteins may result in impaired functionality and/or increased immunogenicity. Another approach focuses on the dissociation of aggregates (referred to as “disaggregation”) to recover functional, native monomers by using various mechanisms such as temperature, pressure, pH, and salts. Currently, protein aggregates are removed as impurities mainly in the polishing steps of downstream processing. However, in cases of high levels of high-molecular weight (HMW), removing significant amount of HMW not only results in substantial yield loss but also makes the design of a robust downstream process challenging (Chi et al., Pharm Res, Vol. 20, No. 9, September 2003, pp. 1325-1336).
Preserving protein stability and activity in biological and biotechnological applications poses serious challenges. There is a need in the art for optimized pharmaceutical compositions that provide for enhanced stabilization of therapeutic proteins and reduce aggregation and denaturation during formulation, filling, shipping, storage and administration, thereby preventing loss-of-function and adverse immunogenic reactions. It is the object of the present invention to comply with thus need.

SUMMARY

Protein instability, and in particular protein aggregation, is an increasing challenge in the biotechnology industry, where aggregation is encountered throughout the lifetime of a therapeutic protein, including during refolding, purification, sterilization, shipping, and storage processes. It is thus the object of the present invention to provide a stable pharmaceutical composition comprising a bispecific single chain antibody construct, binding to a target cell surface antigen via a first binding domain and to the T cell surface antigen CD3 via a second binding domain; a β-cyclodextrin; and a buffer.
The β-cyclodextrin may be present in a selected from the group consisting of β-cyclodextrin, methyl-β-cyclodextrin, hydroxyethyl-β-cyclodextrin, hydroxypropyl-β-cyclodextrin, ethyl-β-cyclodextrin, butyl-β-cyclodextrin Succinyl-(2-hydroxypropyl)-β-cyclodextrin, heptakis(2,3,6-tri-O-methyl)-β-cyclodextrin, heptakis(2,3,6-tri-O-benzoyl)-β-cyclodextrin, β-cyclodextrin phosphate sodium salt, β-cyclodextrin sulphate sodium salt, triacetyl-β-cyclodextrin, heptakis(6-O-sulfo)-β-cyclodextrin heptasodium salt, carboxymethyl-β-cyclodextrin sodium salt, sulfobutylether-β-cyclodextrin sodium salt, 6-O-β-toluenesulfonyl-β-cyclodextrin, and in particular from sulfobutylether-β-cyclodextrin sodium salt, hydroxypropyl-β-cyclodextrin. It may be present in a concentration in the range of 0.1% to 20% (w/v), preferably of 0.5% to 2% (w/v) and more preferably of 0.8% to 1.5% (w/v).
The bispecific single chain antibody construct may be present in a concentration range of 0.1-5 mg/ml, preferably of 0.2-2.5 mg/ml, more preferably of 0.25-1.0 mg/ml. Its first binding domain may bind to CD33. In particular, the amino acid sequence of the first binding domain of the bispecific single chain construct is selected form the group consisting of SEQ ID 99, 109, 119, 128, 137,146, 155, 164 and 173 and the amino acid sequence of the second binding domain of the bispecific single chain construct is selected form the group consisting of SEQ ID NO: 9, 18, 27, 36, 45, 54, 63, 72, 81, 179 and 90.
The buffer may be selected from the group consisting of potassium phosphate, acetic acid/sodium acetate, citric acid/sodium citrate, succinic acid/sodium succinate, tartaric acid/sodium tartrate, histidine/histidine HCl, glycine, Tris, glutamate, acetate and mixtures thereof, and in particular from potassium phosphate, citric acid/sodium citrate, succinic acid, histidine, glutamate, acetate and combinations thereof.
The pH of the pharmaceutical composition may be in the range of 4 to 7.5.
One or more excipients may be present in the pharmaceutical composition provided herein, including sucrose, trehalose, mannitol, sorbitol, arginine, lysine, polysorbate 20, polysorbate 80, poloxamer 188, pluronic and combinations thereof.
The composition may comprise one or more preservatives, particularly benzyl alcohol, chlorobutanol, phenol, meta-cresol, methylparaben, phenoxyethanol, propylparaben thiomerosal. The structure and typical concentration for the use of these preservatives are described in Table 1 of Meyer et al. J Pharm Sci. 96(12), 3155.
Also provided herein is a pharmaceutical composition free of preservatives, comprising a bispecific single chain antibody construct having the amino acid sequence of SEQ ID NO: 100 or 110 and being in a concentration of about 0.5 mg/ml, and further a cyclodextrin being sulfobutylether-β-cyclodextrin sodium salt in a concentration of about 1% (w/v), and further a buffer being potassium phosphate in concentration of about 10 mM, said formulation further comprising sucrose in concentration of about 8% (w/v) of and polysorbate 80 in concentration of about 0.01% (w/v) at a pH of about 6.0.

DESCRIPTION OF THE FIGURES

FIG. 1 : Quantitation of high molecular weight species and conformer by size exclusion uiltra high performance liquid chromatography (SE-UPLC) in AMG 330 (SEQ ID NO: 100)

preparations containing polysorbate

20, 80 or HP-β-CD.

FIGS. 2A-2C: Effect of polysorbate (PS) 20, 80 and HP-β-CD on the amount of non-monomeric species (including conformers, dimers, aggregates) in AMG 330 preparations in function of stress factors: unstressed (FIG. 2A), foaming (FIG. 2B) and 10 freeze/thaw cycles (FIG. 2C). Quantitation of species was achieved by size exclusion ultra high performance chromatography (SE-UPLC). Protein concentration was addressed by the same assay (A280 detection).

FIG. 3 : Concentration dependent effect of HP-β-CD and SBE-β-CD on the aggregation propensity (measured by optical density at 350 nm; optical densities refer to a pathlength of 10 mm) of AMG 103 in presence of 0.9% (V/V) of benzyl alcohol.

FIGS. 4A-4B: Intrinsic fluorescence emission intensity measurements of AMG 103 before (FIG. 4A) and after (FIG. 4B) incubation at 37° C. for 24 hours in presence of 0.9% (V/V) benzyl alcohol.

FIGS. 5A-5B: Predictive models derived from experimental design studies (2-level 4-factor full factorial) describing the effect of increasing concentrations of HP-β-CD (FIG. 5A) and SBE-β-CD (FIG. 5B) on the optical density at 350 nm of AMG 103 (SEQ ID NO: 174) preparations.

FIG. 6 : Assessment of high molecular weight species (HMWS) by size exclusion chromatography in different formulations containing 5 mg/mL CD33_2-hALB (SEQ ID NO: 175).

FIGS. 7A-7C: High molecular weight species formation rate at 25° C. and 37° C. for three different MSLN-hALB (SEQ ID NO: 176) formulations (K60RTrT (FIG. 7A), K60SBESuT (FIG. 7B), and K60RMSuT (FIG. 7C)) determined by the size exclusion chromatography (SEC)

FIG. 8 : Formation of acidic charge variants at 25° C. and 37° C. for three different MSLN-hALB formulations determined by weak cation exchange ultra high performance liquid chromatography (WCX-UPLC)

FIG. 9 . AMG 330 solubility at 40 C in the presence of 12% PEG-3350. Both SBE-β-CD (Captisol) and Alginate (Protanal) increase solubility of aggregated and monomeric AMG 330 when used at higher concentrations. However, SBE-β-CD preferentially solubilizes monomer. The control on the left (1×PBS) was incubated without SBE-β-CD, whereas the control on the right (1×PBS) was incubated without PEG and SBE-β-CD.

FIG. 10 : Data from the same experiment as shown in FIG. 9 that demonstrates the effect of different concentrations of SBE-β-CD and Alginate on % monomer and % aggregate in AMG 330. SBE-β-CD at ˜ 0.1-1% is effective at increasing monomer content at the expense of aggregates (shown by green arrows). In contrast, Alginate data shows opposite trend of increasing aggregates (shown by red arrow). SBE-β-CD was also shown to reduce the negative impact of overconcentration in this case.

FIG. 11 : Average SEC relative peak area of AMG 330 after buffer exchange and protein concentration by ultrafiltration/centrifugation.

FIGS. 12A-12D. FIG. 12A: Summary of maximal AMG 330 concentrations achieved by overconcentration, calculated by SEC mainpeak+HMW. SBE-β-CD formulations (indicated by asterisks) reached higher concentrations and maintained higher % monomer. FIG. 12B: Data from the same experiment as shown in FIG. 12A where AMG 330 was concentrated up to 7-8 mg/mL in the presence of increasing concentrations of SBE-β-CD with or without glycine and sucrose (see asterisks). The control on the left was concentrated without SBE-β-CD. The control on the right was not concentrated beyond its starting concentration of 0.4 mg/ml. Additional sample labeled as ‘2% Glycine, 1% Sucrose” was concentrated without SBE-β-CD to demonstrate the advantage of using SBE-β-CD. FIG. 12C: AMG 330 CEX relative peak areas after 5 days incubation at 4° C., average of two replicates. All samples contain 20 mM citrate, 0.01% PS-80, pH 6.0. FIG. 12D: AMG 330 relative main peak area after SEC analysis. All samples also include 20 mM Citrate, 0.01% PS-80, pH 6.0.

FIG. 13 : AMG 330 concentration calculated from SEC main peak+HMW.

FIG. 14 : AMG 330 relative peak area from SEC after buffer exchange and concentration.

FIG. 15 : AMG 330 SEC total peak areas (main peak+HMW) peak after incubation with various cyclodextrins

FIG. 16 : AMG 330 in 13 different formulations at 1 mg/mL and stored at −20, −30 and −700° C. for up to 6 weeks.

FIGS. 17A-17D: FIG. 17A: Although SBE-β-CD at 0.5% may not be fully sufficient to provide an elegant lyo cake on its own, it is compatible with more common bulking agents, such as glycine and mannitol. All of these lyo cakes reconstituted well and produced little to no aggregation or particulation in the presence of SBE-β-CD. FIG. 17B: The use of SBE-β-CD (blue chromatogram, indicated by arrow) but not α-cyclodextran (pink chromatogram, indicated by arrow) reduces % aggregate post-reconstitution. Control formulation without any cyclodextrin (in thick black line) also shows an elevated level of aggregates, albeit lower than α-cyclodextran. These results demonstrate the advantage of using SBE-β-CD. FIG. 17C: Analytical SEC of different formulations (pre and post representes pre-lyophilization and post-constitution). FIG. 17D: MFI analysis for different formulations following lyophilization.

FIG. 18 . Summary of maximal Fapa BiTE® (SEQ ID NO: 177) concentrations achieved by overconcentration. SBE-β-CD formulations (indicated by asterisks) reached higher protein concentrations compared to α-cyclodextran and maintained higher % monomer. The α-cyclodextran formulations lost most of their soluble protein because of precipitation.

FIG. 19 . Overview on percentage content of high molecular weight species (HMWS) determined by size exclusion ultra-high performance chromatography (SE-UPLC) in function of CD33-scFc BiTE antibody construct formulation.

FIG. 20 . Overview on percentage content of high molecular weight species (HMWS) determined by size exclusion ultra-high performance chromatography (SE-UPLC) in function of FLT3-scFc BiTE antibody construct formulation.

FIG. 21 . Overview on percentage content of high molecular weight species (HMWS) determined by size exclusion ultra-high performance chromatography (SE-UPLC) in function of BCMA-scFc BiTE antibody construct formulation.

DETAILED DESCRIPTION

Despite the high quality of current therapeutic biotech products and the resemblance of recombinant human proteins and antibodies to endogenous human proteins, protein instability remains an important concern. In addition to the quality-related consequences of protein aggregation such as possible loss of protein activity and undesirable aesthetics of drug product, soluble protein aggregates have been reported to have significant cytotoxic effects, and, importantly, are a potential risk factor for the development of an the immune response to protein products.
Protein aggregation can occur during at various points throughout the lifetime of a protein, including fermentation, refolding, purification, filling, shipment, storage or administration and is strongly dependent on various environmental factors. There is a critical need in the art to increase stability and reduce aggregation of therapeutic proteins; and optimized pharmaceutical formulations can aid in doing so. The present inventors investigated the effects of different cyclodextrins to on the aggregation of bispecific antibody constructs (specifically, Bi-specific T-cell engagers, BiTE®) when exposed to various environmental stress factors. Surprisingly, the inventors found that antibody constructs could be significantly stabilized in the presence of cyclodextrins, and in particular β-cyclodextrins.
Thus, the present invention provides a stable pharmaceutical composition comprising a) a bispecific single chain antibody construct, binding to a target cell surface antigen via a first binding domain and to the T cell surface antigen CD3 via a second binding domain, b) a β-cyclodextrin and c) a buffer.

Stability

Within the present invention, the term “stability” or “stabilization” relates to the stability of the pharmaceutical composition in total and in particular to the stability of the active ingredient (i.e. the bispecific single chain antibody construct) itself, specifically during formulation, filling, shipment, storage and administration. The terms “stability” or “stable” in the context of the pharmaceutical composition of the invention and the bispecific single chain antibody construct particularly refers to the reduction or prevention of the formation of protein aggregates (HMWS). Specifically, the term “stability” also relates to the colloidal stability of the bispecific single chain antibody constructs comprised within the pharmaceutical composition described herein. “Colloidal stability” is the ability of colloidal particles (such as proteins) to remain dispersed in liquids for a prolonged period of time (days to years).
The term “(protein) aggregate” as used herein generally encompasses protein species of higher molecular weight such as “oligomers” or “multimers” instead of the desired defined species (e.g., a monomer). The term is used interchangeably herein with the terms “high molecular weight species” and “HMWS”. Protein aggregates may generally differ in size (ranging from small (dimers) to large assemblies (subvisible or even visible particles) and from the nanometer to micrometer range in diameter), morphology (approximately spherical to fibrillar), protein structure (native vs. non-native/denatured), type of intermolecular bonding (covalent vs. non-covalent), reversibility and solubility. Soluble aggregates cover the size range of roughly 1 to 100 nm, and protein particulates cover subvisible (˜0.1-100.m) and visible (>100. m) ranges. All of the aforementioned types protein aggregates are generally encompassed by the term. The term “(protein) aggregate” thus refers to all kinds physically-associated or chemically linked non-native species of two or more protein monomers.
The term “protein aggregation” or “non-native aggregation” thus denotes the process(es) by which protein molecules assemble into complexes composed of two or more proteins, with the individual proteins denoted as the monomer. There are multiple pathways leading to protein aggregation that can be induced by a wide variety of conditions, including temperature, mechanical stress such as shaking and stirring, pumping, freezing and/or thawing and formulation.

Temperature

An increase in temperature accelerates chemical reactions such as oxidation and deamidation of proteins, which can in turn promote aggregation. Higher temperature also directly influences conformation of proteins on the quaternary, tertiary, and secondary structure level, and can lead to temperature-induced unfolding that can promote aggregation.

Freezing and Thawing

Protein denaturation and aggregation can occur during freeze/thawing due to complex physical and chemical changes such as creation of new ice/solution interfaces, adsorption to container surfaces, cryoconcentration of the protein and solutes, and pH changes due to crystallization of buffer components.

Protein Concentration

An increase in protein concentration can also enhance the formation of protein aggregates. At high protein concentrations, macromolecular crowding occurs, a term used to describe the effect of high total volume occupancy by macromolecular solutes upon the behavior of each macromolecular species in that solution. According to this excluded volume theory, self-assembly and thus potentially aggregation may be favored.

Preservatives

Antimicrobial preservatives, such as benzyl alcohol and phenol, are often needed in protein liquid formulations to ensure sterility during its shelf life, and in addition required in multidose formulations and certain drug delivery systems, e.g., injection pens, minipumps and topical applications. Many preservatives have been reported to induce protein aggregation, although the underlying mechanism is not well understood. It has been proposed that preservatives bind to and populate unfolded protein states that are prone to aggregation.
Advantageously, the pharmaceutical compositions of the invention are envisaged to be stable, i.e. to remain free or substantially free from protein aggregates even when subjected to stress, in particular thermal stress, storage, surface-induced stress (such as freeze/thaw cycles, foaming), concentration (by ultra- and diafiltration) or being mixed with organic compounds such as antimicrobial preservatives. Preferably, the pharmaceutical compositions may have similar or even improved characteristics as compared to the compositions comprising SBE-β-CD or HP β-CD that have been evaluated in the appended Examples. Pharmaceutical compositions of the invention are preferably homogenous solutions of dispersed monomeric bispecific single chain antibody constructs.
The skilled person will appreciate that even though the pharmaceutical composition effectively provides for stabilization of the active ingredient (i.e. reduces or inhibits formation of protein aggregates of the bispecific single chain antibody construct), some aggregates or conformers may occasionally form, however without substantially compromising overall usability of the pharmaceutical composition. In this context “substantially free” of aggregates means that the amount of aggregates remains lower than 10%, 9%, 8%, 7%, 6%, 5%, 4%, 3%, 2% or 1% (w/v), particularly also when being subjected to environmental stress, e.g. as evaluated in the appended Examples.
Methods for determining the presence of soluble and insoluble protein aggregates have been, inter alia, reviewed by Mahler et al., J Pharm Sci. 2009 September; 98(9):2909-34. Formation of soluble protein aggregates can be evaluated by size exclusion ultra high performance liquid chromatography (SE-UPLC) as described in the appended Examples. SEC is one of the most used analytical methods for the detection and quantification of protein aggregates. SEC analysis allows both for sizing of aggregates, and their quantification. SEQ-UPLC allows for the selective and rapid separation of macromolecules based on their shape and size (hydrodynamic radius) in a molecular weight range of about 5-1000 kDa.
Protein solutions show an optical property, called opalescence or turbidity. The optical property of a solution is a function of the particles present to scatter and absorb light. Proteins are natural colloids and the turbidity of aqueous formulations depends on protein concentration, the presence of nondissolved particles, particle size and particle number per volume unit. Turbidity can be measured by UV-Vis spectroscopy as optical density in the 340-360 nm range and be used to detect both soluble and insoluble aggregates.
Moreover, the inspection of samples by visual means is still an important aspect of assessing protein aggregates. Visual evaluation for the absence or presence of visible aggregates is preferably performed according to Deutscher Arzneimittel Codex (DAC) Test 5.
As set out elsewhere herein, it is envisaged pharmaceutical composition of the invention—most likely by the action of β-cyclodextrins comprised therein—favor an increased colloidal stability of the bispecific single chain antibody constructs, and thus exhibit a reduced or even absent liquid-liquid phase separation (LLPS). LLPS is a thermodynamically driven event, in which a homogenous protein solution separates into a protein-poor phase (usually the top layer) and a protein-rich phase (usually the bottom layer) with decreasing temperatures. LLPS is typically fully reversible simply by mixing the two phases and raising the temperature of the solution. The occurrence of LLPS has been attributed to short-range attractive protein-protein interactions—making it a measure of strength of protein-protein attraction. Pharmaceutical compositions comprising β-cyclodextrins according to the invention have been found to comprise higher concentrations of the bispecific single chain antibody construct in the LLPS protein-poor phase, as compared to pharmaceutical compositions not comprising β-cyclodextrins. Accordingly, pharmaceutical compositions of the invention are envisaged to exhibit reduced LLPS or no LLPS at all when compared to controls, and thus promoting an increased colloidal stability of the bispecific single chain antibody constructs of the present invention. LLPS can be induced and the protein content of the different phases can be examined as described in the appended Examples.
Environmental stress can, in particular due to thermal and/or chemical denaturation, also lead to conformational changes, which may in turn favor aggregation. Surprisingly, the present inventors found that bispecific single chain antibody constructs are also stabilized with regard to conformational changes as evaluated by measuring intrinsic fluorescence emission intensity of aromatic amino acids. The pharmaceutical composition of the present invention therefore preferably also reduces or inhibits the formation of conformers (i.e. non-native, abnormally folded protein species).

Antibody Construct

As explained previously, the stable pharmaceutical composition of the present invention comprises a bispecific single chain antibody construct, binding to a target cell surface antigen via a first binding domain and to the T Cell surface antigen CD3 via a second binding domain.
The term “antibody construct” generally refers to a molecule in which the structure and/or function is/are based on the structure and/or function of an antibody, e.g. of a full-length or whole immunoglobulin molecule. An antibody construct is hence capable of binding to its specific target or antigen. Furthermore, an antibody construct according to the invention comprises the minimum structural requirements of an antibody which allow for the target binding. This minimum requirement may e.g. be defined by the presence of at least the three light chain CDRs (i.e. CDR1, CDR2 and CDR3 of the VL region) and/or the three heavy chain CDRs (i.e. CDR1, CDR2 and CDR3 of the VH region). The antibodies on which the constructs described herein are based include for example monoclonal, recombinant, chimeric, deimmunized, humanized and human antibodies.
Within the definition of “antibody constructs” are full-length or whole antibodies including camelid antibodies and other immunoglobulin antibodies generated by biotechnological or protein engineering methods or processes. These full-length antibodies may be for example monoclonal, recombinant, chimeric, deimmunized, humanized and human antibodies. Also within the definition of “antibody constructs” are fragments of full-length antibodies, such as VH, VHH, VL, (s)dAb, Fv, Fd, Fab, Fab′, F(ab′)2 or “r IgG” (“half antibody”). Antibody constructs may also be modified fragments of antibodies, also called antibody variants, such as scFv, di-scFv or bi(s)-scFv, scFv-Fc, scFv-zipper, scFab, Fab2, Fab3, diabodies, single chain diabodies, tandem diabodies (Tandab's), tandem di-scFv, tandem tri-scFv, “minibodies” exemplified by a structure which is as follows: (VH-VL-CH3)2, (scFv-CH3)2 or (scFv-CH3-scFv)2, multibodies such as triabodies or tetrabodies, and single domain antibodies such as nanobodies or single variable domain antibodies comprising merely one variable domain, which might be V_HH, V_NARVH or VL, that specifically bind an antigen or epitope independently of other V regions or domains. Also encompassed by the term “antibody construct” are single domain antibody constructs composed of (at least) two single domain monoclonal antibodies which are individually selected from the group comprising VH, VL, V_HH and V_NAR, and a linker. The linker is preferably in the form of a peptide linker. Similarly, an “scFv-single domain mAb” is a monoclonal antibody construct composed of at least one single domain antibody as described above and one scFv molecule as described above. Again, the linker is preferably in the form of a peptide linker.
Furthermore, the definition of the term “antibody constructs” generally includes monovalent, bivalent and polyvalent/multivalent constructs and, thus, monospecific constructs, specifically binding to only one antigenic structure, as well as bispecific and polyspecific/multispecific constructs, which specifically bind more than one antigenic structure, e.g. two, three or more, through distinct binding domains. Moreover, the definition of the term “antibody constructs” includes molecules consisting of only one polypeptide chain as well as molecules consisting of more than one polypeptide chain, which chains can be either identical (homodimers, homotrimers or homo oligomers) or different (heterodimer, heterotrimer or heterooligomer). In the context of the present invention, bispecific single chain antibody constructs binding to a target cell surface antigen via a first binding domain and to the T cell surface antigen CD3 via a second binding domain are particularly envisaged.

Binding Domains

The term “binding domain” characterizes a domain which (specifically) binds to/interacts with/recognizes a given target epitope or a given target site on the target molecules (antigens). Binding domains are preferably in the form of polypeptides. Such polypeptides may include proteinaceous parts and non-proteinaceous parts (e.g. chemical linkers or chemical cross-linking agents such as glutaraldehyde). Proteins (including fragments thereof, preferably biologically active fragments, and peptides, usually having less than 30 amino acids) comprise two or more amino acids coupled to each other via a covalent peptide bond (resulting in a chain of amino acids). The term “polypeptide” as used herein describes a group of molecules, which usually consist of more than 30 amino acids. Polypeptides may further form multimers such as dimers, trimers and higher oligomers, i.e. consisting of more than one polypeptide molecule. Polypeptide molecules forming such dimers, trimers etc. may be identical or non-identical. The corresponding higher order structures of such multimers are, consequently, termed homo- or heterodimers, homo- or heterotrimers etc. An example for a heretero multimer is an antibody molecule, which, in its naturally occurring form, consists of two identical light polypeptide chains and two identical heavy polypeptide chains. The terms “peptide”, “polypeptide” and “protein” also refer to naturally modified peptides/polypeptides/proteins wherein the modification is effected e.g. by post-translational modifications like glycosylation, acetylation, phosphorylation and the like. A “peptide”, “polypeptide” or “protein” when referred to herein may also be chemically modified such as pegylated. Such modifications are well known in the art and described herein below.
The structure and function of the first binding domain, and preferably also the structure and/or function of the second binding domain is based on the structure and/or function of an antibody, e.g. of a full-length or whole immunoglobulin molecule. The first binding domain is characterized by the presence of three light chain CDRs (i.e. CDR1, CDR2 and CDR3 of the variable light (VL) region) and three heavy chain CDRs (i.e. CDR1, CDR2 and CDR3 of the variable heavy (VH) region). The second binding domain preferably also comprises the minimum structural requirements of an antibody which allow for the target binding. More preferably, the second binding domain comprises at least three light chain CDRs (i.e. CDR1, CDR2 and CDR3 of the VL region) and/or three heavy chain CDRs (i.e. CDR1, CDR2 and CDR3 of the VH region).
As mentioned above, a binding domain may typically comprise an antibody light chain variable region (VL) and an antibody heavy chain variable region (VH); however, it does not have to comprise both. Fd fragments, for example, have two VH regions and often retain some antigen-binding function of the intact antigen-binding domain. Examples of (modified) antigen-binding antibody fragments include (1) a Fab fragment, a monovalent fragment having the VL, VH, CL and CH1 domains; (2) a F(ab′)2 fragment, a bivalent fragment having two Fab fragments linked by a disulfide bridge at the hinge region; (3) an Fd fragment having the two VH and CH1 domains; (4) an Fv fragment having the VL and VH domains of a single arm of an antibody, (5) a dAb fragment (Ward et al., (1989) Nature 341:544-546), which has a VH domain; (6) an isolated complementarity determining region (CDR), and (7) a single chain Fv (scFv).

Variable Regions

The term “variable” refers to the portions of the antibody or immunoglobulin domains that exhibit variability in their sequence and that are involved in determining the specificity and binding affinity of a particular antibody (i.e., the “variable domain(s)”). The pairing of a variable heavy chain (VH) and a variable light chain (VL) together forms a single antigen-binding site. The CH domain most proximal to VH is designated as CH1. Each light (L) chain is linked to a heavy (H) chain by one covalent disulfide bond, while the two H chains are linked to each other by one or more disulfide bonds depending on the H chain isotype.
Variability is not evenly distributed throughout the variable domains of antibodies; it is concentrated in sub-domains of each of the heavy and light chain variable regions. These sub-domains are called “hypervariable regions” or “complementarity determining regions” (CDRs). CDRs contain most of the residues responsible for specific interactions of the antibody with the antigen and hence contribute to the functional activity of an antibody molecule: they are the main determinants of antigen specificity.
The exact definitional CDR boundaries and lengths are subject to different classification and numbering systems. CDRs may therefore be referred to by Kabat, Chothia, contact or any other boundary definitions, including the numbering system described herein. Despite differing boundaries, each of these systems has some degree of overlap in what constitutes the so called “hypervariable regions” within the variable sequences. CDR definitions according to these systems may therefore differ in length and boundary areas with respect to the adjacent framework region. See for example Kabat (an approach based on cross-species sequence variability), Chothia (an approach based on crystallographic studies of antigen-antibody complexes), and/or MacCallum (Kabat et al., loc. cit.; Chothia et al., J. Mol. Biol, 1987, 196: 901-917; and MacCallum et al., J. Mol. Biol, 1996, 262: 732). Still another standard for characterizing the antigen binding site is the AbM definition used by Oxford Molecular's AbM antibody modeling software. See, e.g., Protein Sequence and Structure Analysis of Antibody Variable Domains. In: Antibody Engineering Lab Manual (Ed.: Duebel, S. and Kontermann, R., Springer-Verlag, Heidelberg). To the extent that two residue identification techniques define regions of overlapping, but not identical regions, they can be combined to define a hybrid CDR. However, the numbering in accordance with the so-called Kabat system is preferred.
Typically, CDRs form a loop structure that can be classified as a canonical structure. The term “canonical structure” refers to the main chain conformation that is adopted by the antigen binding (CDR) loops. From comparative structural studies, it has been found that five of the six antigen binding loops have only a limited repertoire of available conformations. Each canonical structure can be characterized by the torsion angles of the polypeptide backbone. Correspondent loops between antibodies may, therefore, have very similar three dimensional structures, despite high amino acid sequence variability in most parts of the loops (Chothia and Lesk, J. Mol. Biol., 1987, 196: 901; Chothia et al., Nature, 1989, 342: 877; Martin and Thornton, J. Mol. Biol, 1996, 263: 800). Furthermore, there is a relationship between the adopted loop structure and the amino acid sequences surrounding it. The conformation of a particular canonical class is determined by the length of the loop and the amino acid residues residing at key positions within the loop, as well as within the conserved framework (i.e., outside of the loop). Assignment to a particular canonical class can therefore be made based on the presence of these key amino acid residues.
The term “canonical structure” may also include considerations as to the linear sequence of the antibody, for example, as catalogued by Kabat (Kabat et al., loc. cit.). The Kabat numbering scheme (system) is a widely adopted standard for numbering the amino acid residues of an antibody variable domain in a consistent manner and is the preferred scheme applied in the present invention as also mentioned elsewhere herein. Additional structural considerations can also be used to determine the canonical structure of an antibody. For example, those differences not fully reflected by Kabat numbering can be described by the numbering system of Chothia et al and/or revealed by other techniques, for example, crystallography and two- or three-dimensional computational modeling. Accordingly, a given antibody sequence may be placed into a canonical class which allows for, among other things, identifying appropriate chassis sequences (e.g., based on a desire to include a variety of canonical structures in a library). Kabat numbering of antibody amino acid sequences and structural considerations as described by Chothia et al., loc. cit. and their implications for construing canonical aspects of antibody structure, are described in the literature. The subunit structures and three-dimensional configurations of different classes of immunoglobulins are well known in the art. For a review of the antibody structure, see Antibodies: A Laboratory Manual, Cold Spring Harbor Laboratory, eds. Harlow et al., 1988.
The CDR3 of the light chain and, particularly, the CDR3 of the heavy chain may constitute the most important determinants in antigen binding within the light and heavy chain variable regions. In some antibody constructs, the heavy chain CDR3 appears to constitute the major area of contact between the antigen and the antibody. In vitro selection schemes in which CDR3 alone is varied can be used to vary the binding properties of an antibody or determine which residues contribute to the binding of an antigen. Hence, CDR3 is typically the greatest source of molecular diversity within the antibody-binding site. H3, for example, can be as short as two amino acid residues or greater than 26 amino acids.

Framework and Constant Regions

The more conserved (i.e., non-hypervariable) portions of the variable domains are called the “framework” regions (FRM) and provide a scaffold for the six CDRs in three dimensional space to form an antigen-binding surface. The variable domains of naturally occurring heavy and light chains each comprise four FRM regions (FR1, FR2, FR3, and FR4), largely adopting a β-sheet configuration, connected by three hypervariable regions, which form loops connecting, and in some cases forming part of, the β-sheet structure. The hypervariable regions in each chain are held together in close proximity by the FRM and, with the hypervariable regions from the other chain, contribute to the formation of the antigen-binding site (see Kabat et al., loc. cit.). The constant domains are not directly involved in antigen binding, but exhibit various effector functions, such as, for example, antibody-dependent, cell-mediated cytotoxicity and complement activation.

Binding Specificity

Bispecific Antibody Constructs

As explained previously, the antibody construct comprised within the pharmaceutical composition of the invention is particularly envisaged to be a bispecific single chain antibody construct. The term “bispecific” as used herein refers to an antibody construct which is “at least bispecific”, i.e., it comprises at least a first binding domain and a second binding domain, wherein the first binding domain binds to one antigen or target, and the second binding domain binds to another antigen or target. Accordingly, antibody constructs encompassed by the term comprise specificities for at least two different antigens or targets. The term “bispecific antibody construct” thus also encompasses multispecific antibody constructs such as trispecific antibody constructs, the latter ones including three binding domains, or constructs having more than three (e.g. four, five . . . ) specificities. Given that the antibody constructs are (at least) bispecific, they do not occur naturally and they are markedly different from naturally occurring products. A “bispecific” antibody construct is hence an artificial hybrid antibody or immunoglobulin having at least two distinct binding sites with different specificities. Bispecific antibodies can be produced by a variety of methods known in the art, e.g. by chemical conjugation of two different, purified monoclonal antibodies (mAbs) or antibody fragments or by fusing two hybridomas resulting in a quadroma cell line producing, among others, bispecific IgG molecules (see Kontermann and Brinkmann, Drug Discov Today. 2015 July; 20(7):838-47 for review).

Targets

As set out previously, the pharmaceutical composition of the invention comprises a bispecific single chain antibody construct binding to a target cell surface antigen via a first binding domain and to the T Cell surface antigen CD3 via a second binding domain.
The terms “(specifically) binds to”, (specifically) recognizes”, “is (specifically) directed to”, and “(specifically) reacts with” mean in accordance with this invention that a binding domain interacts or specifically interacts with one or more, preferably at least two, more preferably at least three and most preferably at least four amino acids of an epitope located on the target protein or antigen.
The term “epitope” refers to a site on an antigen to which a binding domain, such as an antibody or immunoglobulin or derivative or fragment of an antibody or of an immunoglobulin, specifically binds. An “epitope” is antigenic and thus the term epitope is sometimes also referred to herein as “antigenic structure” or “antigenic determinant”. Thus, the binding domain is an “antigen interaction site”. Said binding/interaction is also understood to define a “specific recognition”. “Epitopes” can be formed both by contiguous amino acids (linear epitope) or non-contiguous amino acids juxtaposed by tertiary folding of a protein (conformational epitope. Linear epitopes typically includes at least 3 or at least 4, and more usually, at least 5 or at least 6 or at least 7, for example, about 8 to about 10 amino acids in a unique sequence. A conformational epitope typically comprises an increased number of amino acids relative to a linear epitope. Methods of determining the conformation of epitopes include, but are not limited to, x-ray crystallography, two-dimensional nuclear magnetic resonance (2D-NMR) spectroscopy and site-directed spin labelling and electron paramagnetic resonance (EPR) spectroscopy.
The interaction between the binding domain and the epitope or epitope cluster implies that a binding domain exhibits appreciable affinity for the epitope or epitope cluster on a particular protein or antigen and, generally, does not exhibit significant reactivity with non-target proteins or antigens. “Appreciable affinity” includes binding with an affinity of about 10⁻⁶M (KD) or stronger. Preferably, binding is considered specific when the binding affinity is about 10⁻¹²to 10⁻⁸M, 10⁻¹²to 10⁻⁹M, 10⁻¹²to 10⁻¹⁰M, 10⁻¹¹to 10⁻⁸M, preferably of about 10⁻¹¹to 10⁻⁹M. Preferably, a binding domain of the invention does not essentially or substantially bind to proteins or antigens other than its target proteins or antigens (i.e., the first binding and second binding domain are not capable of binding to proteins other than their respective target protein).
The term “does not essentially/substantially bind” or “is not capable of binding” means that a binding domain of the present invention does not bind a protein or antigen other than its target protein or antigen, i.e., does not show reactivity of more than 30%, preferably not more than 20%, more preferably not more than 10%, particularly preferably not more than 9%, 8%, 7%, 6% or 5% with proteins or antigens other than its target protein or antigen, whereby binding to its respective target protein or antigen is set to be 100%.
As explained herein, the bispecific single chain antibody construct is envisaged to comprise a first binding domain capable of binding to a target cell surface antigen and a second binding domain capable of binding to the T Cell surface antigen CD3. The antibody construct, the binding domains and in particular the second binding domain (which binds to human CD3 on the surface of a T cell) is in particular envisaged to have the following format: The pairs of VH regions and VL regions are in the format of a single chain antibody (scFv). The VH and VL regions are arranged in the order VH-VL or VL-VH. It is preferred that the VH-region is positioned N-terminally to a linker sequence, and the VL-region is positioned C-terminally of the linker sequence.
The second binding domain of the antibody construct comprised within the pharmaceutical composition of the invention is capable of binding to the T Cell surface antigen CD3. T cells or T lymphocytes are a type of lymphocyte (itself a type of white blood cell) that play a central role in cell-mediated immunity. There are several subsets of T cells, each with a distinct function. T cells can be distinguished from other lymphocytes, such as B cells and NK cells, by the presence of a T cell receptor (TCR) on the cell surface. The TCR is responsible for recognizing antigens bound to major histocompatibility complex (MHC) molecules and is composed of two different protein chains. In 95% of the T cells, the TCR consists of an alpha (α) and beta (β) chain. When the TCR engages with antigenic peptide and MHC (peptide/MHC complex), the T lymphocyte is activated through a series of biochemical events mediated by associated enzymes, co-receptors, specialized adaptor molecules, and activated or released transcription factors
The CD3 receptor complex is a protein complex and is composed of four chains. In mammals, the complex contains a CD3γ (gamma) chain, a CD3δ (delta) chain, and two CD3ε (epsilon) chains. These chains associate with the T cell receptor (TCR) and the so-called ζ (zeta) chain to form the T cell receptor CD3 complex and to generate an activation signal in T lymphocytes. The CD3γ (gamma), CD3δ (delta), and CD3ε (epsilon) chains are highly related cell-surface proteins of the immunoglobulin superfamily containing a single extracellular immunoglobulin domain. The intracellular tails of the CD3 molecules contain a single conserved motif known as an immunoreceptor tyrosine-based activation motif or ITAM for short, which is essential for the signaling capacity of the TCR. The CD3 epsilon molecule is a polypeptide which in humans is encoded by the CD3E gene which resides on chromosome 11.
The second binding domain of the bispecific single chain antibody construct comprised within the pharmaceutical composition of the invention is capable of binding to a target cell surface antigen. Said target cell surface antigen may in general be any antigen that can be recognized by and bind to the second binding domain. The bispecific single chain antibody construct is envisaged to form a link between T cells and target cells by binding to both CD3 and the target cell surface antigen. The bispecific single chain antibody construct is thus thought to recruit T cells to target cells, and preferably to cause T cells to exert cytotoxic activity on target cells by producing pro-apoptotic proteins like perforin and granzymes, thereby causing target cell. The target cell will therefore typically be a cell intended as a target for T cell mediated cytotoxicity and, hence, cytolysis. For instance, the target cell may be a tumor cell such as a malignant blast cell. The target cell surface antigen may thus be selected from CD33, CD19, FAPalpha, MSLN, FLT3 or BCMA. CD33 is particularly envisaged as a target for the first binding domain of the bispecific single chain antibody construct of the invention.
Preferred bispecific single chain antibody constructs of the present invention include AMG 103 (comprising a first binding domain recognizing CD19), AMG 330 (comprising a first binding domain recognizing CD33) a CD33 specific HLE BiTE, a FLT3 specific HLE BiTE and a BCMA specific HLE BiTE as evaluated in the appended Examples.
Specifically, the amino acid sequence of the first binding domain of the bispecific single chain construct may be selected form the group consisting of SEQ ID 99, 109, 119, 128, 137,146, 155, 164, 173, 183, 185 and 187 and the amino acid sequence of the second binding domain of the bispecific single chain construct may be selected form the group consisting of SEQ ID NO: 9, 18, 27, 36, 45, 54, 63, 72, 81, 179 and 90.
Preferred bispecific single chain antibody constructs of the invention thus include constructs comprising or consisting of polypeptide having an amino acid sequence as depicted in a SEQ ID NO selected from the group consisting of SEQ ID NO:100, SEQ ID NO:110, SEQ ID NO:174, SEQ ID NO:175, SEQ ID NO:176, SEQ ID NO:177, SEQ ID NO:180, SEQ ID NO:182, SEQ ID NO:184, SEQ ID NO:186, SEQ ID NO:188.

Peptide Linkers

The at least two binding domains and the variable domains of the antibody construct of the present invention may or may not comprise peptide linkers (spacer peptides). The term “peptide linker” defines in accordance with the present invention an amino acid sequence by which the amino acid sequences of one (variable and/or binding) domain and another (variable and/or binding) domain of the antibody construct of the invention are linked with each other. An essential technical feature of such peptide linker is that said peptide linker does not comprise any polymerization activity. Among the suitable peptide linkers are those described in U.S. Pat. Nos. 4,751,180 and 4,935,233 or WO 88/09344.
In the event that a linker is used, this linker is preferably of a length and sequence sufficient to ensure that each of the first and second domains can, independently from one another, retain their differential binding specificities. For peptide linkers which connect the at least two binding domains in the antibody construct (or two variable domains), those peptide linkers may comprise only a few number of amino acid residues, e.g. 12 amino acid residues or less, such as 11, 10, 9, 8, 7, 6 or 5 amino acid residues. An envisaged peptide linker with less than 5 amino acids comprises 4, 3, 2 or one amino acid(s) and may be Gly-rich, i.e. may consist of the single amino acid Gly. Other useful peptide linker are characterized by the amino acid sequence Gly-Gly-Gly-Gly-Ser (SEQ ID NO: 178), i.e. Gly₄Ser, or polymers thereof, i.e. (Gly₄Ser)x, where x is an integer of 1 or greater. Preferably, peptide linkers do not promote any secondary structures are preferred. Methods for preparing fused and operatively linked bispecific single chain constructs and expressing them in mammalian cells or bacteria are well-known in the art (e.g. Sambrook et al., Molecular Cloning: A Laboratory Manual, 4^thed., Cold Spring Harbor Laboratory Press, Cold Spring Harbor, N.Y., 2012).

Derivatives

The term “antibody construct” also encompasses derivatives. The term “derivative” generally refers to an antibody construct that has been covalently modified to introduce an additional functionality. Covalent modifications of the antibody constructs can be introduced post-translationally by reacting specific amino acid residues of the molecule with an organic derivatizing agent that is capable of reacting with selected side chains or the N- or C-terminal residues. Derivatization of antibody constructs can be used to attach therapeutic or diagnostic agents, labels, groups extending the serum half-life of the molecule, or insertion of non-natural amino acids. Commonly applied chemical modifications include the following:
Cysteinyl residues most commonly are reacted with α-haloacetates (and corresponding amines), such as chloroacetic acid or chloroacetamide, to give carboxymethyl or carboxyamidomethyl derivatives. Cysteinyl residues also are derivatized by reaction with bromotrifluoroacetone, α-bromo-β-(5-imidozoyl)propionic acid, chloroacetyl phosphate, N-alkylmaleimides, 3-nitro-2-pyridyl disulfide, methyl 2-pyridyl disulfide, p-chloromercuribenzoate, 2-chloromercuri-4-nitrophenol, or chloro-7-nitrobenzo-2-oxa-1,3-diazole.
Histidyl residues are derivatized by reaction with diethylpyrocarbonate at pH 5.5-7.0 because this agent is relatively specific for the histidyl side chain. Para-bromophenacyl bromide also is useful; the reaction is preferably performed in 0.1 M sodium cacodylate at pH 6.0. Lysinyl and amino terminal residues are reacted with succinic or other carboxylic acid anhydrides. Derivatization with these agents has the effect of reversing the charge of the lysinyl residues. Other suitable reagents for derivatizing alpha-amino-containing residues include imidoesters such as methyl picolinimidate; pyridoxal phosphate; pyridoxal; chloroborohydride; trinitrobenzenesulfonic acid; O-methylisourea; 2,4-pentanedione; and transaminase-catalyzed reaction with glyoxylate.
Arginyl residues are modified by reaction with one or several conventional reagents, among them phenylglyoxal, 2,3-butanedione, 1,2-cyclohexanedione, and ninhydrin. Derivatization of arginine residues requires that the reaction be performed in alkaline conditions because of the high pKa of the guanidine functional group. Furthermore, these reagents may react with the groups of lysine as well as the arginine epsilon-amino group.
The specific modification of tyrosyl residues may be made, with particular interest in introducing spectral labels into tyrosyl residues by reaction with aromatic diazonium compounds or tetranitromethane. Most commonly, N-acetylimidizole and tetranitromethane are used to form O-acetyl tyrosyl species and 3-nitro derivatives, respectively. Tyrosyl residues are iodinated using ¹²⁵I or ¹³¹I to prepare labeled proteins for use in radioimmunoassay, the chloramine T method described above being suitable.
Carboxyl side groups (aspartyl or glutamyl) are selectively modified by reaction with carbodiimides (R′—N═C═N—R′), where R and R′ are optionally different alkyl groups, such as 1-cyclohexyl-3-(2-morpholinyl-4-ethyl) carbodiimide or 1-ethyl-3-(4-azonia-4,4-dimethylpentyl) carbodiimide. Furthermore, aspartyl and glutamyl residues are converted to asparaginyl and glutaminyl residues by reaction with ammonium ions.
Derivatization with bifunctional agents is useful for crosslinking the antibody constructs of the present invention to a water-insoluble support matrix or surface for use in a variety of methods. Commonly used crosslinking agents include, e.g., 1,1-bis(diazoacetyl)-2-phenylethane, glutaraldehyde, N-hydroxysuccinimide esters, for example, esters with 4-azidosalicylic acid, homobifunctional imidoesters, including disuccinimidyl esters such as 3,3′-dithiobis(succinimidylpropionate), and bifunctional maleimides such as bis-N-maleimido-1,8-octane. Derivatizing agents such as methyl-3-[(p-azidophenyl)dithio]propioimidate yield photoactivatable intermediates that are capable of forming crosslinks in the presence of light. Alternatively, reactive water-insoluble matrices such as cyanogen bromide-activated carbohydrates and the reactive substrates described in U.S. Pat. Nos. 3,969,287; 3,691,016; 4,195,128; 4,247,642; 4,229,537; and 4,330,440 are employed for protein immobilization.
Glutaminyl and asparaginyl residues are frequently deamidated to the corresponding glutamyl and aspartyl residues, respectively. Alternatively, these residues are deamidated under mildly acidic conditions. Either form of these residues falls within the scope of this invention.
Other modifications include hydroxylation of proline and lysine, phosphorylation of hydroxyl groups of seryl or threonyl residues, methylation of the α-amino groups of lysine, arginine, and histidine side chains (T. E. Creighton, Proteins: Structure and Molecular Properties, W. H. Freeman & Co., San Francisco, 1983, pp. 79-86), acetylation of the N-terminal amine, and amidation of any C-terminal carboxyl group.

Glycosylation and De-Glycosylation

Another type of covalent modification of the antibody constructs included within the scope of this invention comprises altering the glycosylation pattern of the protein. As is known in the art, glycosylation patterns can depend on both the sequence of the protein (e.g., the presence or absence of particular glycosylation amino acid residues, discussed below), or the host cell or organism in which the protein is produced. Particular expression systems are discussed below.
Glycosylation of polypeptides is typically either N-linked or O-linked. N-linked refers to the attachment of the carbohydrate moiety to the side chain of an asparagine residue. The tri-peptide sequences asparagine-X-serine and asparagine-X-threonine, where X is any amino acid except proline, are the recognition sequences for enzymatic attachment of the carbohydrate moiety to the asparagine side chain. Thus, the presence of either of these tri-peptide sequences in a polypeptide creates a potential glycosylation site. O-linked glycosylation refers to the attachment of one of the sugars N-acetylgalactosamine, galactose, or xylose, to a hydroxyamino acid, most commonly serine or threonine, although 5-hydroxyproline or 5-hydroxylysine may also be used.
Addition of glycosylation sites to the antibody construct is conveniently accomplished by altering the amino acid sequence such that it contains one or more of the above-described tri-peptide sequences (for N-linked glycosylation sites). The alteration may also be made by the addition of, or substitution by, one or more serine or threonine residues to the starting sequence (for O-linked glycosylation sites). For ease, the amino acid sequence of an antibody construct is preferably altered through changes at the DNA level, particularly by mutating the DNA encoding the polypeptide at preselected bases such that codons are generated that will translate into the desired amino acids.
Another means of increasing the number of carbohydrate moieties on the antibody construct is by chemical or enzymatic coupling of glycosides to the protein. These procedures are advantageous in that they do not require production of the protein in a host cell that has glycosylation capabilities for N- and O-linked glycosylation. Depending on the coupling mode used, the sugar(s) may be attached to (a) arginine and histidine, (b) free carboxyl groups, (c) free sulfhydryl groups such as those of cysteine, (d) free hydroxyl groups such as those of serine, threonine, or hydroxyproline, (e) aromatic residues such as those of phenylalanine, tyrosine, or tryptophan, or (f) the amide group of glutamine. These methods are described in WO 87/05330, and in Aplin and Wriston, 1981, CRC Crit. Rev. Biochem., pp. 259-306.
Removal of carbohydrate moieties present on the starting antibody construct may be accomplished chemically or enzymatically. Chemical deglycosylation requires exposure of the protein to the compound trifluoromethanesulfonic acid, or an equivalent compound. This treatment results in the cleavage of most or all sugars except the linking sugar (N-acetylglucosamine or N-acetylgalactosamine), while leaving the polypeptide intact. Chemical deglycosylation is described by Hakimuddin et al., 1987, Arch. Biochem. Biophys. 259:52 and by Edge et al., 1981, Anal. Biochem. 118:131. Enzymatic cleavage of carbohydrate moieties on polypeptides can be achieved by the use of a variety of endo- and exo-glycosidases as described by Thotakura et al., 1987, Meth. Enzymol. 138:350. Glycosylation at potential glycosylation sites may be prevented by the use of the compound tunicamycin as described by Duskin et al., 1982, J. Biol. Chem. 257:3105. Tunicamycin blocks the formation of protein-N-glycoside linkages.

Non-Proteinaceous Polymers

Other modifications of the antibody construct are contemplated herein. For example, another type of covalent modification of the antibody construct comprises linking the antibody construct to various non-proteinaceous polymers, including, but not limited to, various polyols such as various polyols such as polyethylene glycol (PEGylation), polypropylene glycol, polyoxyalkylenes, or copolymers of polyethylene glycol and polypropylene glycol, or of carbohydrates, such as hydroxyethyl starch (e.g., HESylation®) or polysialic acid (e.g., PolyXen® technology. In addition, as is known in the art, amino acid substitutions may be made in various positions within the antibody construct, e.g. in order to facilitate the addition of polymers such as PEG.

Labels

In some embodiments, the covalent modification of the antibody constructs of the invention comprises the addition of one or more labels. The labelling group may be coupled to the antibody construct via spacer arms of various lengths to reduce potential steric hindrance. Various methods for labelling proteins are known in the art and can be used in performing the present invention. The term “label” or “labelling group” refers to any detectable label. In general, labels fall into a variety of classes, depending on the assay in which they are to be detected—the following examples include, but are not limited to:

- a) isotopic labels, which may be radioactive or heavy isotopes, such as radioisotopes or radionuclides (e.g., ³H, ¹⁴C ¹⁵N, ³⁵S, ⁸⁹Zr, ⁹⁰Y, ⁹⁹Tc, ¹¹¹In, ¹²⁵I, ¹³¹I)
- b) magnetic labels (e.g., magnetic particles)
- c) redox active moieties
- d) optical dye (including, but not limited to, chromophores, phosphors and fluorophores) such as fluorescent groups (e.g., FITC, rhodamine, lanthanide phosphors), chemiluminescent groups, and fluorophores which can be either “small molecule” fluores or proteinaceous fluores
- e) enzymatic groups (e.g. horseradish peroxidase, β-galactosidase, luciferase, alkaline phosphatase)
- f) biotinylated groups
- g) predetermined polypeptide epitopes recognized by a secondary reporter (e.g., leucine zipper pair sequences, binding sites for secondary antibodies, metal binding domains, epitope tags, etc.)

By “fluorescent label” is meant any molecule that may be detected via its inherent fluorescent properties. Suitable fluorescent labels include, but are not limited to, fluorescein, rhodamine, tetramethylrhodamine, eosin, erythrosin, coumarin, methyl-coumarins, pyrene, Malacite green, stilbene, Lucifer Yellow, Cascade BlueJ, Texas Red, IAEDANS, EDANS, BODIPY FL, LC Red 640, Cy 5, Cy 5.5, LC Red 705, Oregon green, the Alexa-Fluor dyes (Alexa Fluor 350, Alexa Fluor 430, Alexa Fluor 488, Alexa Fluor 546, Alexa Fluor 568, Alexa Fluor 594, Alexa Fluor 633, Alexa Fluor 660, Alexa Fluor 680), Cascade Blue, Cascade Yellow and R-phycoerythrin (PE) (Molecular Probes, Eugene, Oreg.), FITC, Rhodamine, and Texas Red (Pierce, Rockford, Ill.), Cy5, Cy5.5, Cy7 (Amersham Life Science, Pittsburgh, Pa.). Suitable optical dyes, including fluorophores, are described in Molecular Probes Handbook by Richard P. Haugland.
Suitable proteinaceous fluorescent labels also include, but are not limited to, green fluorescent protein, including a Renilla, Ptilosarcus, or Aequorea species of GFP (Chalfie et al., 1994, Science 263:802-805), EGFP (Clontech Laboratories, Inc., Genbank Accession Number U55762), blue fluorescent protein (BFP, Quantum Biotechnologies, Inc. 1801 de Maisonneuve Blvd. West, 8th Floor, Montreal, Quebec, Canada H3H 1J9; Stauber, 1998, Biotechniques 24:462-471; Heim et al., 1996, Curr. Biol. 6:178-182), enhanced yellow fluorescent protein (EYFP, Clontech Laboratories, Inc.), luciferase (Ichiki et al., 1993, J. Immunol. 150:5408-5417), β galactosidase (Nolan et al., 1988, Proc. Natl. Acad. Sci. U.S.A. 85:2603-2607) and Renilla (WO92/15673, WO95/07463, WO98/14605, WO98/26277, WO99/49019, U.S. Pat. Nos. 5,292,658, 5,418,155, 5,683,888, 5,741,668, 5,777,079, 5,804,387, 5,874,304, 5,876,995, 5,925,558).
Leucine zipper domains are peptides that promote oligomerization of the proteins in which they are found. Leucine zippers were originally identified in several DNA-binding proteins (Landschulz et al., 1988, Science 240:1759), and have since been found in a variety of different proteins. Among the known leucine zippers are naturally occurring peptides and derivatives thereof that dimerize or trimerize. Examples of leucine zipper domains suitable for producing soluble oligomeric proteins are described in PCT application WO 94/10308, and the leucine zipper derived from lung surfactant protein D (SPD) described in Hoppe et al., 1994, FEBS Letters 344:191. The use of a modified leucine zipper that allows for stable trimerization of a heterologous protein fused thereto is described in Fanslow et al., 1994, Semin. Immunol. 6:267-78. In one approach, recombinant fusion proteins comprising CDH19 antibody fragment or derivative fused to a leucine zipper peptide are expressed in suitable host cells, and the soluble oligomeric CDH19 antibody fragments or derivatives that form are recovered from the culture supernatant.
The antibody construct may also comprise additional peptides or domains, which are e.g. helpful in the isolation of the molecule or relate to an adapted pharmacokinetic profile of the molecule. Domains helpful for the isolation of an antibody construct may be selected from peptide motives or secondarily introduced moieties, which can be captured in an isolation method, e.g. an isolation column. Non-limiting embodiments of such additional domains comprise peptide motives known as Myc-tag, HAT-tag, HA-tag, TAP-tag, GST-tag, chitin binding domain (CBD-tag), maltose binding protein (MBP-tag), Flag-tag, Strep-tag and variants thereof (e.g. StrepII-tag) and His-tag. His-tag domains are generally known as a repeat of consecutive His residues in the amino acid sequence of a molecule, preferably of six His residues. Domains or peptides useful for extending the serum half-life (i.e. the time where 50% of an administered drug are eliminated through biological processes, e.g. metabolism, excretion, etc.) of the antibody constructs include those capable of binding to other proteins with a preferred pharmacokinetic profile in the human body such as serum albumin (e.g. the AB156 peptide) or the constant region of immunoglobulins (Fc domains or variants thereof).
The bispecific single chain antibody construct is envisaged to be present in the pharmaceutical composition of the invention in a concentration of up to about 5 mg/mL, i.e. about 4.0 mg/mL, 3.0 mg/mL, 2.0 mg/mL, 1.0 mg/mL, 0.5 mg/mL, 0.25 mg/mL or 0.1 mg/mL. Preferably, the bispecific single chain antibody construct is present in the pharmaceutical composition in a concentration between 0.1 to 5 mg/mL, preferably of 0.2-2.5 mg/mL, more preferably of 0.25-1.0 mg/mL.

Cyclodextrins

Besides the bispecific single chain antibody construct and the buffer, the pharmaceutical composition of the present invention further comprises a β-cyclodextrin. In general, the term “cyclodextrin” or “CD” refers to a cyclic oligosaccharides composed of at least 6 or more 1→4 linked α-D-glucopyranoside units. The unitary structure of the cyclodextrins is characterized by a hydrophobic cavity with ether groups inside and a polar exterior which is characterized by primary hydroxyl groups. Many cyclodextrins are known in the art, including 6-membered (α-cyclodextrins), 7-membered (β-cyclodextrins) and 8-membered (γ-cylodextrins) cyclodextrins. β-cyclodextrins comprising 7 α-D-glucopyranoside units are particularly preferred components of the pharmaceutical composition of the invention, as they have been shown to be capable of effectively stabilizing the bispecific single chain antibody constructs under various stress conditions.
The term “cyclodextrin” (and in particular “β-cyclodextrin”) also encompasses chemically modified (β-)cyclodextrin derivatives. In general, any chemical modification is conceivable as long as it does not reduce or abolish the advantageous properties of the pharmaceutical composition as demonstrated in the appended examples, and in particular as long as the pharmaceutical compositions retains its stability. Chemically modified cyclodextrin derivatins typically result from etherification or the introduction of other functional groups at the 2-, 3- and 6-hydroxyl groups of the glucose residues. Thus, the term includes cyclodextrins comprising one or more substitutions of the hydroxyl groups, e.g. alkylated and hydroxyalkylated cyclodextrins.
For the purpose of the invention, the term “cyclodextrin” also includes pharmaceutically acceptable salt(s) thereof. The phrase “pharmaceutically acceptable salt(s)”, as used herein, means those salts of cyclodextrins that are safe and effective for the administration. Pharmaceutically acceptable salts include those formed with anions such as those derived from hydrochloric, phosphoric, acetic, oxalic, tartaric acids, etc., and those formed with cations such as those derived from sodium, potassium, ammonium, calcium, ferric hydroxides, isopropylamine, triethylamine, 2-ethylamino ethanol, histidine, procaine, etc. Of course, any counterions used in pharmaceuticals must be considered safe, and several lists of pharmaceutically approved counterions exist, which vary depending on the source. Approved salt formers can e.g. be found in the Handbook of Pharmaceutical Salts (Stahl P H, Wermuth C G, editors. 2002. Handbook of pharmaceutical salts: Properties, selection and use. Weinheim/Zurich: Wiley-VCH/VHCA.).
Thus, the pharmaceutical composition of the invention is envisaged to comprise a β-cyclodextrin, particularly one selected from the group consisting of β-cyclodextrin, methyl-β-cyclodextrin, hydroxyethyl-β-cyclodextrin, hydroxypropyl-β-cyclodextrin, ethyl-β-cyclodextrin, butyl-β-cyclodextrin Succinyl-(2-hydroxypropyl)-β-cyclodextrin, heptakis(2,3,6-tri-O-methyl)-β-cyclodextrin, heptakis(2,3,6-tri-O-benzoyl)-β-cyclodextrin, β-cyclodextrin phosphate sodium salt, β-cyclodextrin sulphate sodium salt, triacetyl-β-cyclodextrin, heptakis(6-O-sulfo)-β-cyclodextrin heptasodium salt, carboxymethyl-β-cyclodextrin sodium salt, sulfobutylether-β-cyclodextrin sodium salt, and 6-O-β-toluenesulfonyl-β-cyclodextrin. In particular, the β-cyclodextrin may be sulfobutylether-β-cyclodextrin (“SBE-β-CD”) sodium salt, hydroxypropyl-β-cyclodextrin (“HP-β-CD”).
The β-cyclodextrin may be present in the pharmaceutical composition in a concentration in the range of 0.1% to 20% (w/v), preferably of 0.5% to 2% (w/v) and more preferably of 0.8% to 1.5% (w/v). It is in particular envisaged that the concentration of chemically unmodified β-cyclodextrin is about 1.8% (w/v) or less, such as about 1.6% (w/v), about 1.5% (w/v), about 1.4% (w/v), about 1.3% (w/v), about 1.2% (w/v), about 1.1% (w/v), about 1.0% (w/v), about 0.9% (w/v), about 0.8% (w/v), or less, down to a concentration of about 0.1% (w/v).

Buffer

The pharmaceutical composition of the invention further comprises a buffer, which may be selected from the group consisting of potassium phosphate, acetic acid/sodium acetate, citric acid/sodium citrate, succinic acid/sodium succinate, tartaric acid/sodium tartrate, histidine/histidine HCl, glycine, Tris, glutamate, acetate and mixtures thereof, and in particular from potassium phosphate, citric acid/sodium citrate, succinic acid, histidine, glutamate, acetate and combinations thereof.
Suitable buffer concentrations encompass concentrations of about 200 mM or less, such as about 190, 180, 170, 160, 150, 140, 130, 120, 110, 100, 80, 70, 60, 50, 40, 30, 20, 10 or 5 mM. The skilled person will be readily able to adjust the buffer concentrations in order to provide for stability of the pharmaceutical composition as described herein. Envisaged buffer concentrations in the pharmaceutical composition of the invention specifically range from about 5 to about 200 mM, preferably from about 5 to about 100 mM, and more preferably from about 10 to about 50 mM.
pH
The pharmaceutical composition according to the invention may have a pH in the range from about 4 to about 7.5, i.e. a pH of 4, 4.5, 5, 5.5, 6, 6.5, 7 or 7.5. Preferably, the pH is in the range from about 5 to about 7.5, more preferably from about 5.5 to about 7.5.

Pharmaceutical Composition

As used herein, the term “pharmaceutical composition” relates to a composition which is suitable for administration to a subject in need thereof. The terms “subject” or “individual” or “animal” or “patient” are used interchangeably herein to refer to any subject, particularly a mammalian subject, for whom administration of the pharmaceutical composition of the invention is desired. Mammalian subjects include humans, non-human primates, dogs, cats, guinea pigs, rabbits, rats, mice, horses, cattle, cows, and the like, with humans being preferred. The pharmaceutical composition of the present invention is stable and pharmaceutically acceptable, i.e. capable of eliciting the desired therapeutic effect without causing any undesirable local or systemic effects in the subject to which the pharmaceutical composition is administered. Pharmaceutically acceptable compositions of the invention may in particular be sterile and/or pharmaceutically inert. Specifically, the term “pharmaceutically acceptable” can mean approved by a regulatory agency or other generally recognized pharmacopoeia for use in animals, and more particularly in humans.
The pharmaceutical composition of the invention comprises one or a plurality of the bispecific single chain antibody construct(s) described herein, preferably in a therapeutically effective amount, a β-cyclodextrin and a buffer. By “therapeutically effective amount” is meant an amount of said construct that elicits the desired therapeutic effect. Therapeutic efficacy and toxicity can be determined by standard pharmaceutical procedures in cell cultures or experimental animals, e.g., ED₅₀(the dose therapeutically effective in 50% of the population) and LD₅₀(the dose lethal to 50% of the population). The dose ratio between therapeutic and toxic effects is the therapeutic index, and it can be expressed as the ratio, ED₅₀/LD₅₀. Pharmaceutical compositions that exhibit large therapeutic indices are generally preferred.

Excipients

Besides the β-cyclodextrin and the buffer described previously, the pharmaceutical composition may optionally comprise one or more further excipients as long as they do not reduce or abolish its advantageous properties as described herein, and in particular its stability.
Excipients can be used in the invention for a wide variety of purposes, such as adjusting physical, chemical, or biological properties of formulations, such as adjustment of viscosity, and or processes of the invention to further improve effectiveness and or to further stabilize such formulations and processes against degradation and spoilage due to, for instance, stresses that occur during manufacturing, shipping, storage, pre-use preparation, administration, and thereafter. The term “excipient” generally includes fillers, binders, disintegrants, coatings, sorbents, antiadherents, glidants, preservatives, antioxidants, flavoring, coloring, sweeting agents, solvents, co-solvents, buffering agents, chelating agents, viscosity imparting agents, surface active agents, diluents, humectants, carriers, diluents, preservatives, emulsifiers, stabilizers and tonicity modifiers.
Acceptable excipients are preferably pharmaceutically acceptable, i.e. nontoxic to recipients at the dosages and concentrations employed.
Exemplary excipients include, without limitation:

- amino acids such as glycine, alanine, glutamine, asparagine, threonine, proline, 2-phenylalanine, including charged amino acids, preferably lysine, lysine acetate, arginine, glutamate and/or histidine
- preservatives, including antimicrobials such as antibacterial and antifungal agents
- antioxidants such as ascorbic acid, methionine, sodium sulfite or sodium hydrogen-sulfite;
- buffers, buffer systems and buffering agents which are used to maintain the composition at physiological pH or at a slightly lower pH, typically within a pH range of from about 5 to about 8 or 9; examples of buffers are borate, bicarbonate, Tris-HCl, citrates, phosphates or other organic acids, succinate, phosphate, histidine and acetate; for example Tris buffer of about pH 7.0-8.5, or acetate buffer of about pH 4.0-5.5;
- non-aqueous solvents such as propylene glycol, polyethylene glycol, vegetable oils such as olive oil, and injectable organic esters such as ethyl oleate;
- aqueous carriers including water, alcoholic/aqueous solutions, emulsions or suspensions, including saline and buffered media;
- biodegradable polymers such as polyesters;
- bulking agents such as mannitol or glycine;
- chelating agents such as ethylenediamine tetraacetic acid (EDTA);
- isotonic and absorption delaying agents;
- complexing agents such as caffeine, polyvinylpyrrolidone, beta-cyclodextrin or hydroxypropyl-beta-cyclodextrin)
- fillers;
- monosaccharides; disaccharides; and other carbohydrates (such as glucose, mannose or dextrins); carbohydrates may be non-reducing sugars, preferably trehalose, sucrose, octasulfate, sorbitol or xylitol;
- (low molecular weight) proteins, polypeptides or proteinaceous carriers such as human or bovine serum albumin, gelatin or immunoglobulins, preferably of human origin;
- coloring and flavouring agents;
- sulfur containing reducing agents, such as glutathione, thioctic acid, sodium thioglycolate, thioglycerol, [alpha]-monothioglycerol, and sodium thio sulfate
- diluting agents;
- emulsifying agents;
- hydrophilic polymers such as polyvinylpyrrolidone)
- salt-forming counter-ions such as sodium;
- preservatives such as antimicrobials, anti-oxidants, chelating agents, inert gases and the like; examples are: benzalkonium chloride, benzoic acid, salicylic acid, thimerosal, phenethyl alcohol, methylparaben, propylparaben, chlorhexidine, sorbic acid or hydrogen peroxide);
- metal complexes such as Zn-protein complexes;
- solvents and co-solvents (such as glycerin, propylene glycol or polyethylene glycol);
- sugars and sugar alcohols, including polyols, trehalose, sucrose, octasulfate, mannitol, sorbitol or xylitol stachyose, mannose, sorbose, xylose, ribose, myoinisitose, galactose, lactitol, ribitol, myoinisitol, galactitol, glycerol, cyclitols (e.g., inositol), polyethylene glycol; and polyhydric sugar alcohols;
- suspending agents;
- surfactants or wetting agents such as pluronics, PEG, sorbitan esters, polysorbates such as polysorbate 20, polysorbate, triton, tromethamine, lecithin, cholesterol, tyloxapal; surfactants may be detergents, preferably with a molecular weight of >1.2 KD and/or a polyether, preferably with a molecular weight of >3 KD; non-limiting examples for preferred detergents are Tween 20, Tween 40, Tween 60, Tween 80 and Tween 85; non-limiting examples for preferred polyethers are PEG 3000, PEG 3350, PEG 4000 and PEG 5000;
- stability enhancing agents such as sucrose or sorbitol;
- tonicity enhancing agents such as alkali metal halides, preferably sodium or potassium chloride, mannitol sorbitol;
- parenteral delivery vehicles including sodium chloride solution, Ringers dextrose, dextrose and sodium chloride, lactated Ringer's, or fixed oils;
- intravenous delivery vehicles including fluid and nutrient replenishers, electrolyte replenishers (such as those based on Ringer's dextrose).

It is evident to those skilled in the art that the different excipients of the pharmaceutical composition (e.g., those listed above) can have different effects, for example, and amino acid can act as a buffer, a stabilizer and/or an antioxidant; mannitol can act as a bulking agent and/or a tonicity enhancing agent; sodium chloride can act as delivery vehicle and/or tonicity enhancing agent; etc.
Polyols are useful stabilizing agents in both liquid and lyophilized formulations to protect proteins from physical and chemical degradation processes, and are also useful for adjusting the tonicity of formulations. Polyols include sugars, e.g., mannitol, sucrose, and sorbitol and polyhydric alcohols such as, for instance, glycerol and propylene glycol, and, for purposes of discussion herein, polyethylene glycol (PEG) and related substances. Mannitol is commonly used to ensure structural stability of the cake in lyophilized formulations. It ensures structural stability to the cake. It is generally used with a lyoprotectant, e.g., sucrose. Sorbitol and sucrose are commonly used agents for adjusting tonicity and as stabilizers to protect against freeze-thaw stresses during transport or the preparation of bulks during the manufacturing process. PEG is useful to stabilize proteins and as a cryoprotectant.
Surfactants routinely are used to prevent, minimize, or reduce surface adsorption. Protein molecules may be susceptible to adsorption on surfaces and to denaturation and consequent aggregation at air-liquid, solid-liquid, and liquid-liquid interfaces. These effects generally scale inversely with protein concentration. These deleterious interactions generally scale inversely with protein concentration and typically are exacerbated by physical agitation, such as that generated during the shipping and handling of a product. Commonly used surfactants include polysorbate 20, polysorbate 80, other fatty acid esters of sorbitan polyethoxylates, and poloxamer 188. Surfactants also are commonly used to control protein conformational stability. The use of surfactants in this regard is protein-specific since, any given surfactant typically will stabilize some proteins and destabilize others.
Polysorbates are susceptible to oxidative degradation and often, as supplied, contain sufficient quantities of peroxides to cause oxidation of protein residue side-chains, especially methionine. Consequently, polysorbates should be used carefully, and when used, should be employed at their lowest effective concentration.
Antioxidants can—to some extent—prevent deleterious oxidation of proteins in pharmaceutical formulations by maintaining proper levels of ambient oxygen and temperature and by avoiding exposure to light. Antioxidant excipients can be used as well to prevent oxidative degradation of proteins. Among useful antioxidants in this regard are reducing agents, oxygen/free-radical scavengers, and chelating agents. Antioxidants for use in therapeutic protein formulations are preferably water-soluble and maintain their activity throughout the shelf life of a product. EDTA is a useful example.
Metal ions can act as protein co-factors and enable the formation of protein coordination complexes. Metal ions also can inhibit some processes that degrade proteins. However, metal ions also catalyze physical and chemical processes that degrade proteins. Magnesium ions (10-120 mM) can be used to inhibit isomerization of aspartic acid to isoaspartic acid. Ca⁺²ions (up to 100 mM) can increase the stability of human deoxyribonuclease. Mg⁺², Mn⁺², and Zn⁺², however, can destabilize rhDNase. Similarly, Ca⁺²and Sr⁺²can stabilize Factor VIII, it can be destabilized by Mg⁺², Mn⁺²and Zn⁺², Cu⁺²and Fe⁺², and its aggregation can be increased by Al⁺³ions.
Preservatives have the primary function to inhibit microbial growth and ensure product sterility throughout the shelf-life or term of use of the drug product, and are in particular needed for multi-dose formulations. Commonly used preservatives include benzyl alcohol, phenol and m-cresol. Although preservatives have a long history of use with small-molecule parenterals, the development of protein formulations that includes preservatives can be challenging. Preservatives almost always have a destabilizing effect (aggregation) on proteins, and this has become a major factor in limiting their use in protein formulations. To date, most protein drugs have been formulated for single-use only. However, when multi-dose formulations are possible, they have the added advantage of enabling patient convenience, and increased marketability. A good example is that of human growth hormone (hGH) where the development of preserved formulations has led to commercialization of more convenient, multi-use injection pen presentations.
As might be expected, development of liquid formulations containing preservatives are more challenging than lyophilized formulations. Freeze-dried products can be lyophilized without the preservative and reconstituted with a preservative containing diluent at the time of use. This shortens the time for which a preservative is in contact with the protein, significantly minimizing the associated stability risks. With liquid formulations, preservative effectiveness and stability should be maintained over the entire product shelf-life (about 18 to 24 months). An important point to note is that preservative effectiveness should be demonstrated in the final formulation containing the active drug and all excipient components.
Salts may be used in accordance with the invention to, for example, adjust the ionic strength and/or the isotonicity of the pharmaceutical formulation and/or to further improve the solubility and/or physical stability of the antibody construct or other ingredient. As is well known, ions can stabilize the native state of proteins by binding to charged residues on the protein's surface and by shielding charged and polar groups in the protein and reducing the strength of their electrostatic interactions, attractive, and repulsive interactions. Ions also can stabilize the denatured state of a protein by binding to, in particular, the denatured peptide linkages (—CONH) of the protein. Furthermore, ionic interaction with charged and polar groups in a protein also can reduce intermolecular electrostatic interactions and, thereby, prevent or reduce protein aggregation and insolubility. Ionic species differ in their effects on proteins. A number of categorical rankings of ions and their effects on proteins have been developed that can be used in formulating pharmaceutical compositions in accordance with the invention. One example is the Hofmeister series, which ranks ionic and polar non-ionic solutes by their effect on the conformational stability of proteins in solution. Stabilizing solutes are referred to as “kosmotropic.” Destabilizing solutes are referred to as “chaotropic.” Kosmotropes commonly are used at high concentrations (e.g., >1 molar ammonium sulfate) to precipitate proteins from solution (“salting-out”). Chaotropes commonly are used to denture and/or to solubilize proteins (“salting-in”). The relative effectiveness of ions to “salt-in” and “salt-out” defines their position in the Hofmeister series.
Free amino acids can be used in the pharmaceutical composition as bulking agents, stabilizers, and antioxidants, as well as other standard uses. Lysine, proline, serine, and alanine can be used for stabilizing proteins in a formulation. Glycine is useful in lyophilization to ensure correct cake structure and properties. Arginine may be useful to inhibit protein aggregation, in both liquid and lyophilized formulations. Methionine is useful as an antioxidant.
Particularly useful excipients for formulating the pharmaceutical composition include sucrose, trehalose, mannitol, sorbitol, arginine, lysine, polysorbate 20, polysorbate 80, poloxamer 188, pluronic and combinations thereof. Said excipients may be present in the pharmaceutical composition in different concentrations, as long as the composition exhibits the desirable properties as exemplified herein, and in particular promotes stabilization of the contained bispecific single chain antibody constructs. For instance, sucrose may be present in the pharmaceutical composition in a concentration between 2% (w/v) and 12% (w/v), i.e. in a concentration of 12% (w/v), 11% (w/v), 10% (w/v), 9% (w/v), 8% (w/v), 7% (w/v), 6% (w/v), 5% (w/v), 4% (w/v), 3% (w/v) or 2% (w/v). Preferred sucrose concentrations range between 4% (w/v) and 10% (w/v) and more preferably between 6% (w/v) and 10% (w/v). Polysorbate 80 may be present in the pharmaceutical composition in a concentration between 0.001% (w/v) and 0.5% (w/v), i.e. in a concentration of 0.5% (w/v), 0.2% (w/v), 0.1% (w/v), 0.08% (w/v), 0.05% (w/v), 0.02% (w/v), 0.01% (w/v), 0.008% (w/v), 0.005% (w/v), 0.002% (w/v) or 0.001% (w/v). Preferred Polysorbate 80 concentrations range between 0.002% (w/v) and 0.5% (w/v), and preferably between 0.005% (w/v) and 0.02% (w/v).
The pharmaceutical composition provided herein may in particular comprise one or more preservatives.
Useful preservatives for formulating pharmaceutical compositions generally include antimicrobials (e.g. anti-bacterial or anti-fungal agents), anti-oxidants, chelating agents, inert gases and the like; examples are: benzalkonium chloride, benzoic acid, salicylic acid, thimerosal, phenethyl alcohol, methylparaben, propylparaben, chlorhexidine, sorbic acid or hydrogen peroxide). Antimicrobial preservatives are substances which are used to extend the shelf-life of medicines by reducing microbial proliferation. Preservatives that particularly useful for formulating the pharmaceutical composition of the invention include benzyl alcohol, chlorobutanol, phenol, meta-cresol, methylparaben, phenoxyethanol, propylparaben thiomerosal. The structure and typical concentration for the use of these preservatives are described in Table 1 of Meyer et al. J Pharm Sci. 96(12), 3155.
The aforementioned preservatives may be present in the pharmaceutical composition in different concentrations. For instance, benzyl alcohol may be present in a concentration ranging between 0.2 and 1.1% (v/v), chlorobutanol in a concentration ranging between 0.3-0.5% (v/v), phenol in a concentration ranging between 0.07 and 0.5% (v/v), meta-cresol in a concentration ranging between 0.17 and 0-32% (v/v) or thiomerosal in a concentration ranging between 0.003 to 0.01% (v/v). Preferred concentrations for methylparaben are in the range of 0.05 and 0.5% (v/v), for phenoxyethanol in the range of 0.1 and 3% (v/v) and for propylparaben in the range of 0.05 and 0.5% (v/v).
However, it is also conceivable that the pharmaceutical composition does not comprise any preservatives. In particular, the present invention inter alia provides a pharmaceutical composition being free of preservatives, comprising a bispecific single chain antibody construct having an amino acid sequence as depicted in SEQ ID Nos. 100 and 110 in a concentration of about 0.5 mg/ml, sulfobutylether-β-cyclodextrin sodium salt in a concentration of about 1% (w/v), and potassium phosphate in concentration of about 10 mM, and further sucrose in concentration of about 8% (w/v) of and polysorbate 80 in concentration of about 0.01% (w/v) at a pH of about 6.0.

Form

The pharmaceutical compositions of the invention can be formulated in various forms, e.g. in solid, liquid, frozen, gaseous or lyophilized form and may be, inter alia, in the form of an ointment, a cream, transdermal patches, a gel, powder, a tablet, solution, an aerosol, granules, pills, suspensions, emulsions, capsules, syrups, liquids, elixirs, extracts, tincture or fluid extracts.
Generally, various storage and/or dosage forms are conceivable for the pharmaceutical composition of the invention, depending, i.a., on the intended route of administration, delivery format and desired dosage (see, for example, Remington's Pharmaceutical Sciences, 22nd edition, Oslo, A., Ed., (2012)). The skilled person will be aware that such choice of a particular dosage form may for example influence the physical state, stability, rate of in vivo release and rate of in vivo clearance of the antibody construct of the invention.
For instance, the primary vehicle or carrier in a pharmaceutical composition may be either aqueous or non-aqueous in nature. A suitable vehicle or carrier may be water for injection, physiological saline solution or artificial cerebrospinal fluid, possibly supplemented with other materials common in compositions for parenteral administration. Neutral buffered saline or saline mixed with serum albumin are further exemplary vehicles.
When parenteral administration is contemplated, the therapeutic compositions of the invention may be provided in the form of a pyrogen-free, parenterally acceptable aqueous solution comprising the desired antibody construct in a pharmaceutically acceptable vehicle. A particularly suitable vehicle for parenteral injection is sterile distilled water in which the antibody construct is formulated as a sterile, isotonic solution, properly preserved. The preparation can involve the formulation of the desired molecule with an agent, such as injectable microspheres, bio-erodible particles, polymeric compounds (such as polylactic acid or polyglycolic acid), beads or liposomes, that may provide controlled or sustained release of the product which can be delivered via depot injection. Hyaluronic acid may also be used, having the effect of promoting sustained duration in the circulation. Implantable drug delivery devices may be used to introduce the desired antibody construct.
Sustained- or controlled-delivery/release formulations are also envisaged herein. Techniques for formulating a variety of other sustained- or controlled-delivery means, such as liposome carriers, bio-erodible microparticles or porous beads and depot injections, are also known to those skilled in the art. See, for example, International Patent Application No. PCT/US93/00829, which describes controlled release of porous polymeric microparticles for delivery of pharmaceutical compositions. Sustained-release preparations may include semipermeable polymer matrices in the form of shaped articles, e.g., films, or microcapsules. Sustained release matrices may include polyesters, hydrogels, polylactides (as disclosed in U.S. Pat. No. 3,773,919 and European Patent Application Publication No. EP 058481), copolymers of L-glutamic acid and gamma ethyl-L-glutamate (Sidman et al., 1983, Biopolymers 2:547-556), poly (2-hydroxyethyl-methacrylate) (Langer et al., 1981, J. Biomed. Mater. Res. 15:167-277 and Langer, 1982, Chem. Tech. 12:98-105), ethylene vinyl acetate (Langer et al., 1981, supra) or poly-D(−)-3-hydroxybutyric acid (European Patent Application Publication No. EP 133,988). Sustained release compositions may also include liposomes that can be prepared by any of several methods known in the art. See, e.g., Eppstein et al., 1985, Proc. Natl. Acad. Sci. U.S.A. 82:3688-3692; European Patent Application Publication Nos. EP 036,676; EP 088,046 and EP 143,949. The antibody construct may also be entrapped in microcapsules prepared, for example, by coacervation techniques or by interfacial polymerization (for example, hydroxymethylcellulose or gelatine-microcapsules and poly (methylmethacylate) microcapsules, respectively), in colloidal drug delivery systems (for example, liposomes, albumin microspheres, microemulsions, nanoparticles and nanocapsules), or in macroemulsions. Such techniques are disclosed in Remington's Pharmaceutical Sciences, 22nd edition, Oslo, A., Ed., (2012).
Pharmaceutical compositions used for in vivo administration are typically provided as sterile preparations. Sterilization can be accomplished by filtration through sterile filtration membranes. When the composition is lyophilized, sterilization using this method may be conducted either prior to or following lyophilization and reconstitution. Compositions for parenteral administration can be stored in lyophilized form or in a solution. Parenteral compositions generally are placed into a container having a sterile access port, for example, an intravenous solution bag or vial having a stopper pierceable by a hypodermic injection needle.
The antibody constructs disclosed herein may also be formulated as immuno-liposomes. A “liposome” is a small vesicle composed of various types of lipids, phospholipids and/or surfactant which is useful for delivery of a drug to a mammal. The components of the liposome are commonly arranged in a bilayer formation, similar to the lipid arrangement of biological membranes. Liposomes containing the antibody construct are prepared by methods known in the art, such as described in Epstein et al., Proc. Natl. Acad. Sci. USA, 82: 3688 (1985); Hwang et al., Proc. Natl Acad. Sci. USA, 77: 4030 (1980); U.S. Pat. Nos. 4,485,045 and 4,544,545; and WO 97/38731. Liposomes with enhanced circulation time are disclosed in U.S. Pat. No. 5,013,556. Particularly useful liposomes can be generated by the reverse phase evaporation method with a lipid composition comprising phosphatidylcholine, cholesterol and PEG-derivatized phosphatidylethanolamine (PEG-PE). Liposomes are extruded through filters of defined pore size to yield liposomes with the desired diameter. Fab′ fragments of the antibody construct of the present invention can be conjugated to the liposomes as described in Martin et al. J. Biol. Chem. 257: 286-288 (1982) via a disulfide interchange reaction. A chemotherapeutic agent is optionally contained within the liposome. See Gabizon et al. J. National Cancer Inst. 81 (19) 1484 (1989).

Further Active Agents

It is envisaged that the composition of the invention might comprise, in addition to the bispecific single chained antibody construct defined herein, further biologically active agents, depending on the intended use of the composition. Such agents might be in particular drugs acting on tumors and/or malignant cells, but other active agents are also conceivable depending on the intended use of the pharmaceutical composition, including agents acting on the gastro-intestinal system, drugs inhibiting immunoreactions (e.g. corticosteroids), drugs modulating the inflammatory response, drugs acting on the circulatory system and/or agents such as cytokines known in the art. It is also envisaged that the pharmaceutical composition of the present invention is applied in a co-therapy, i.e., in combination with another anti-cancer medicament.

Storage

Once the pharmaceutical composition has been formulated, it may be stored in sterile vials as a solution, suspension, gel, emulsion, solid, crystal, or as a dehydrated or lyophilized powder. Such formulations may be stored either in a ready-to-use form or in a form (e.g., lyophilized) that is reconstituted prior to administration. E.g., lyophilized compositions may be reconstituted in, e.g., bacteriostatic water for injection (BWFI), physiological saline, phosphate buffered saline (PBS), or the same formulation the protein had been in prior to lyophilization.

Route of Administration

The pharmaceutical composition of the invention may in general be formulated for delivery by any suitable route of administration. In the context of the present invention, the routes of administration include, but are not limited to topical routes (such as epicutaneous, inhalational, nasal, opthalmic, auricular/aural, vaginal, mucosal); enteral routes (such as oral, gastrointestinal, sublingual, sublabial, buccal, rectal); and parenteral routes (such as intravenous, intraarterial, intraosseous, intramuscular, intracerebral, intracerebroventricular, epidural, intrathecal, subcutaneous, intraperitoneal, extra-amniotic, intraarticular, intracardiac, intradermal, intralesional, intrauterine, intravesical, intravitreal, transdermal, intranasal, transmucosal, intrasynovial, intraluminal).
The pharmaceutical compositions described herein are particularly useful for parenteral administration, e.g., subcutaneous or intravenous delivery, for example by injection such as bolus injection, or by infusion such as continuous infusion. Pharmaceutical compositions may be administered using a medical device. Examples of medical devices for administering pharmaceutical compositions are described in U.S. Pat. Nos. 4,475,196; 4,439,196; 4,447,224; 4,447, 233; 4,486,194; 4,487,603; 4,596,556; 4,790,824; 4,941,880; 5,064,413; 5,312,335; 5,312,335; 5,383,851; and 5,399,163.
The pharmaceutical composition of the invention can also be administered uninterruptedly. As a non-limiting example, uninterrupted or substantially uninterrupted, i.e. continuous administration may be realized by a small pump system worn by the patient for metering the influx of the antibody construct into the body of the patient. The pharmaceutical composition can be administered by using said pump systems. Such pump systems are generally known in the art, and commonly rely on periodic exchange of cartridges containing the therapeutic agent to be infused. When exchanging the cartridge in such a pump system, a temporary interruption of the otherwise uninterrupted flow of therapeutic agent into the body of the patient may ensue. In such a case, the phase of administration prior to cartridge replacement and the phase of administration following cartridge replacement would still be considered within the meaning of the pharmaceutical means and methods of the invention together make up one “uninterrupted administration” of such therapeutic agent.
The continuous or uninterrupted administration of the pharmaceutical composition of the invention may be intravenous or subcutaneous by way of a fluid delivery device or small pump system including a fluid driving mechanism for driving fluid out of a reservoir and an actuating mechanism for actuating the driving mechanism. Pump systems for subcutaneous administration may include a needle or a cannula for penetrating the skin of a patient and delivering the suitable composition into the patient's body. Said pump systems may be directly fixed or attached to the skin of the patient independently of a vein, artery or blood vessel, thereby allowing a direct contact between the pump system and the skin of the patient. The pump system can be attached to the skin of the patient for 24 hours up to several days. The pump system may be of small size with a reservoir for small volumes. As a non-limiting example, the volume of the reservoir for the suitable pharmaceutical composition to be administered can be between 0.1 and 50 ml.
Continuous administration may also be achieved transdermally by way of a patch worn on the skin and replaced at intervals. One of skill in the art is aware of patch systems for drug delivery suitable for this purpose. It is of note that transdermal administration is especially amenable to uninterrupted administration, as exchange of a first exhausted patch can advantageously be accomplished simultaneously with the placement of a new, second patch, for example on the surface of the skin immediately adjacent to the first exhausted patch and immediately prior to removal of the first exhausted patch. Issues of flow interruption or power cell failure do not arise.
The skilled person will readily understand that the pharmaceutical composition of the invention may in general comprise any of the aforementioned excipients, or additional active agents, or may be provided in any suitable form as long as it is stable and preferably exhibits the same advantageous properties as the pharmaceutical compositions comprising β-cyclodextrins that have been evaluated in the appended Examples. The skilled person will readily be able to adjust the various components so as to provide a pharmaceutical composition that is stable, i.e. is preferably substantially free from aggregates and/or conformers of the bispecific single chain antibody fragments comprised within.
It must be noted that as used herein, the singular forms “a”, “an”, and “the”, include plural references unless the context clearly indicates otherwise. Thus, for example, reference to “a reagent” includes one or more of such different reagents and reference to “the method” includes reference to equivalent steps and methods known to those of ordinary skill in the art that could be modified or substituted for the methods described herein.
Unless otherwise indicated, the term “at least” preceding a series of elements is to be understood to refer to every element in the series. Those skilled in the art will recognize, or be able to ascertain using no more than routine experimentation, many equivalents to the specific embodiments of the invention described herein. Such equivalents are intended to be encompassed by the present invention.
The term “and/or” wherever used herein includes the meaning of “and”, “or” and “all or any other combination of the elements connected by said term”.
The term “about” or “approximately” as used herein means within 20%, preferably within 10%, and more preferably within 5% of a given value or range. It includes, however, also the concrete number, e.g., about 20 includes 20.
The term “less than” or “greater than” includes the concrete number. For example, less than 20 means less than or equal to. Similarly, more than or greater than means more than or equal to, or greater than or equal to, respectively.
Throughout this specification and the claims which follow, unless the context requires otherwise, the word “comprise”, and variations such as “comprises” and “comprising”, will be understood to imply the inclusion of a stated integer or step or group of integers or steps but not the exclusion of any other integer or step or group of integer or step. When used herein the term “comprising” can be substituted with the term “containing” or “including” or sometimes when used herein with the term “having”.
When used herein “consisting of” excludes any element, step, or ingredient not specified in the claim element. When used herein, “consisting essentially of” does not exclude materials or steps that do not materially affect the basic and novel characteristics of the claim.
In each instance herein any of the terms “comprising”, “consisting essentially of” and “consisting of” may be replaced with either of the other two terms.
It should be understood that this invention is not limited to the particular methodology, protocols, material, reagents, and substances, etc., described herein and as such can vary. The terminology used herein is for the purpose of describing particular embodiments only, and is not intended to limit the scope of the present invention, which is defined solely by the claims.
All publications and patents cited throughout the text of this specification (including all patents, patent applications, scientific publications, manufacturer's specifications, instructions, etc.), whether supra or infra, are hereby incorporated by reference in their entirety. Nothing herein is to be construed as an admission that the invention is not entitled to antedate such disclosure by virtue of prior invention. To the extent the material incorporated by reference contradicts or is inconsistent with this specification, the specification will supersede any such material.
A better understanding of the present invention and of its advantages will be obtained from the following examples, offered for illustrative purposes only. The examples are not intended to limit the scope of the present invention in any way.

EXAMPLES

Example 1: Effect of Temperature-Induced Stress on Formulations Comprising AMG330 and HP-β-CD

AMG 330 protein pool (SEQ ID NO: 100) derived from hydroxyapatite chromatography was dialyzed into a formulation base buffer composed of 100 mM tris base, 50 mM disodium hydrogen phosphate, 4% (w/v) trehalose dihydrate at pH 5.2. The endpoint of dialysis was verified by osmolality measurements. The dialyzed bulk was concentrated by ultrafiltration and centrifugation to a concentration of 0.96 mg/mL and sterile filtered by means of a 0.2 μm PVDF filter. The preformulated bulk was divided into three equally sized volume fractions. These were adjusted to pH 5.2, 5.6 and 6.0 respectively using 5M sodium hydroxide and again filtered with a 0.2 μm PVDF filter. After pH adjustment preformulated bulks were spiked with the required volumes of stock solutions containing either 1% (w/V) polysorbate 20, 1% (w/V) polysorbate 80 or 4% (w/V) HP-β-CD. The concentrations of polysorbate 20, polysorbate 80 and HP-β-CD in the final formulations are shown in FIG. 1 . The concentration of each formulation was adjusted to 0.4 mg/mL using base buffer composed as described above. All excipients were applied in compendial grade. The final formulations were filled to 150 μL in polypropylene reaction tubes and incubated in a controlled cabinet at 30° C. for 72 hours. The content of conformer and high molecular weight species (HMWS) was determined with size exclusion ultra high performance liquid chromatography (SE-UPLC). SE-UPLC was performed on an Aquity H-Class UPLC system (Waters) using an Acquity UPLC BEH200 SEC 150 mm column (Waters). Column temperature was set to 25° C. Separation of size variants was achieved by applying an isocratic method with a flow rate of 0.4 mL/min. The mobile phase was composed of 100 mM sodium phosphate, 250 mM NaCl pH 6.8. The run time totals 6.0 minutes. Samples were held at 8° C. within the autosampler until analysis. The injection volume was 7.5 μL. In order to avoid carry over an intermediate injection with 40% ACN was performed after each sample. Detection was based on fluorescence (Ex 280 nm, Em 325 nm). Peak integration was performed using Empower® software. Relative AUC of monomer and size variants was reported. It could be shown that the formation of non-monomeric protein species (including conformers and high molecular weight species) during thermal stress (30° C.) can be inhibited in presence of HP-β-CD (FIG. 1 ). In contrast formulations containing polysorbate 20 or 80 exhibited formation of non-monomeric species over time.

Example 2: Effect of Surface-Induced Stress on Formulations Comprising AMG330 and HP-β-CD

A further experiment was performed in order to assess whether HP-β-CD stabilizes AMG 330 against surface induced stress conditions. AMG 330 drug substance formulated in 35 mM tris hydrochloride, 17.5 mM sodium phosphate hydrogenphosphate, 100 mM L-arginine hydrochloride and 1.4% (w/V) trehalose dihydrate, pH 6.0 was supplemented with either polysorbate 20, 80 or HP-β-CD at different concentrations depicted in FIGS. 2A-2C (x-axis). All excipients were applied in compendial grade. Formulations were filled to 1.0 mL in prewashed and presterilized type I glass vials. Vials were stoppered with sterilized butyl rubber stoppers and were sealed with aluminum caps. Formulations were stressed by (1) ten consecutive freeze/thaw cycles and (2) foaming. Freezing and thawing was performed in an Epsilon 2-6D pilot scale lyophilizer (Christ, Germany). Target temperatures for freezing and thawing were set to −50° C. and 20° C. respectively. Freezing and thawing rates of 0.3 K/min. were used. Each temperature was followed by a 1 hour isothermal plateau. Foaming was achieved by injecting nitrogen into the respective solution over 1 hour at 80 mL per minute using a 21G injection needle. The vial was vented using a second injection needle equipped with sterile filter. Samples stored at −70° C. were used as non-stressed controls. Samples were analyzed by SE-UPLC and visible inspection according Deutscher Arzneimittel Codex (DAC) test 5. SE-UPLC was performed as described under Example 1. For the assessment of protein concentration detection was additionally performed via absorption at 280 nm. In the unstressed control samples it became evident that non-monomeric species including conformer, dimers and aggregates are more abundant in formulations containing polysorbate 20 or 80 if compared to formulations with HP-β-CD. When stressed by foaming and freeze/thaw, non-monomeric species increased in formulations containing polysorbates (FIGS. 2A-2C). The use of HP-β-CD reduced the formation of non-monomeric species. In absence of any surfactant, protein losses greater than 80% were observed whereas the use of polysorbate and HP-β-CD resulted in quantitative protein recovery. In contrast to surfactant free formulations, HP-β-CD containing formulations were practically free of protein aggregates in the visible size range (Table 1).

TABLE 1

Assessment of visible particles according to PhEur 2.9.20.
Inspection result ratings assigned according to Deutscher
Arzneimittel Codex (DAC) test 5.

	%	Inspection	Fulfillment of compendial requirement
Treatment	HP-β-CD	Result	(DAC test 5)¹

unstressed	0.1	4	yes
unstressed	0.5	0	yes
unstressed	1	1	yes
unstressed	2	3	yes
unstressed	without	22	no
10 x F/T	0.1	4	yes
10 x F/T	0.5	2	yes
10 x F/T	1	2	yes
10 x F/T	2	4	yes
10 x F/T	without	30	no
Foaming	0.1	6	no
Foaming	0.5	2	yes
Foaming	1	4	yes
Foaming	2	3	yes
Foaming	without	30	no

¹Compendial requirement according to Deutscher Arzneimittel Codex (DAC) test 5: inspection result < 4.5

Example 3: Effect of Benzyl Alcohol on Formulations Comprising AMG103 and HP-β-CD or SBE-β-CD

The impact of HP-β-CD and SBE-β-CD on the stability of BiTE® antibody constructs in presence of benzyl alcohol was investigated in formulations containing 0.6 mg/mL AMG 103 (blinatumomab). Therefore AMG 103 was formulated in 20 mM histidine, 2% (w/v) trehalose dihydrate, 0.9% (w/v) sodium chloride at pH 7.0. This formulation was supplemented with different concentrations of either HP-β-CD (0.5 and 1.0% w/V) or SBE-β-CD (0.5, 1.0 and 2.0% w/V). A cyclodextrin free formulation served as control. The AMG 103 concentration in all formulations was adjusted to 0.6 mg/mL. All excipients were applied in compendial grade. All formulations were spiked with 0.9% (V/V) benzyl alcohol and filled to 0.5 mL in polypropylene reaction tubes. Incubation was performed at 37° C. for 24 hours. Samples were analyzed by UV absorption to determine the optical density at 350 nm as a measure for protein aggregation and by intrinsic fluorescence emission intensity measurement in order to detect potential conformational changes. UV absorption was performed on an Infinite M1000 plate reader (Tecan) using transparent half area 96 well plates (Corning). Each well was filled with 100 μL of sample solution. Sample measurements were performed in triplicates. UV absorption was recorded at 350 nm. Intrinsic fluorescence emission intensities were analyzed in the same plate from the bottom. Excitation was realized at 278 nm. Emission intensity was recorded from 300 to 500 nm using 1 nm increments. Excitation and emission slits were set to 10 and 5 nm respectively. During both UV and fluorescence measurements the plate was temperature controlled (25° C.).
Optical densities (OD) at 350 nm indicated a reduced aggregation propensity of AMG 103 in presence of HP-β-CD or SBE-β-CD. The effect was more pronounced with increasing cyclodextrin concentrations (FIG. 3 ). The aggregation of AMG 103 in presence of benzyl alcohol translates into a change of the local environment tryptophan residues demonstrated by intrinsic fluorescence. These changes were minimized with increasing concentrations of the different β-CDs (FIG. 4 ).

Example 4: Effect of Benzyl Alcohol on Formulations Comprising Different Concentrations of AMG103 and β-CD

The effect of increased concentrations of HP-β-CD and SBE-β-CD on the aggregation propensity of AMG 103 (blinatumomab) was addressed by a 2-level 4-factor full factorial experimental design. AMG 103 was formulated as described under Example 2. However its concentration was varied between 0.2 and 0.6 mg/mL (Table 2).

TABLE 2

2-level, 4-factor full factorial experimental design to assess the effect
of SBE-β-CD and HP-β-CD on the aggregation
propensity of AMG 103 in presence of benzyl alcohol

	β-CD	AMG	103	Benzyl alcohol
β-CD	concentration	concentration	concentration
type	% w/V	mg/mL	% V/V

HP-β-CD	0.2	0.2	0.5
			0.9
		0.6	0.5
			0.9
	0.6	0.2	0.5
			0.9
		0.6	0.5
			0.9
SBE-β-CD	0.2	0.2	0.5
			0.9
		0.6	0.5
			0.9
	0.6	0.2	0.5
			0.9
		0.6	0.5
			0.9

All samples were incubated directly in a transparent half area 96 well plates (Corning) at 37° C. for 96 hours. The plate was covered with an adhesive foil to avoid evaporation losses. Again optical densities at 350 nm were taken as a measure for aggregation of AMG 103 (see Example 3). Analytical data were evaluated via analysis of variance (ANOVA) using Statistica® software. The normal distribution of measured values was graphically verified by plotting expected normal values against raw residuals. Predictive models (FIGS. 5A-5B) were generated by Statistica® based on regression of analytical data. Thereby, pure factor effects as well as linear interactions between factors were taken into account. At given concentrations of AMG 103 and benzyl alcohol, aggregation of AMG 103 could be reduced with increasing contents of either HP-β-CD or SBE-β-CD (FIGS. 5A-5B).

Example 5: Effect of Storage-Induced Stress on Formulations Comprising Bispecific Antibody Constructs and β-CD

Preformulated drug substance containing approximately 1 mg/mL CD33_2-hALB in 20 mM potassium phosphate, 150 mM L-arginine hydrochloride and 6% (w/V) trehalose dihydrate at pH 6.0 was dialyzed in 20 mM citric acid, 6% (w/V) sucrose at pH 5.0 and in 20 mM potassium phosphate, 6% (w/V) sucrose at pH 6.0 respectively. The dialysis endpoint was determined via osmolality measurements. Dialysis was performed using Slide A Lyzer® devices. After dialysis the citrate buffered material was directly concentrated above 7 mg/mL with VivaSpin® units. Centrifugation was performed at approximately 2000 g for 5 min. at 2 to 8° C. The potassium phosphate buffered material was treated likewise. However the material was divided into two equally sized volume fractions prior to the centrifugation step. One fraction was adjusted to pH 7.0. The pH of the second fraction was maintained at pH 6.0. After sterile filtration through a 0.2 μm PVDF filter, the concentrates were finally formulated by adding stock solutions of polysorbate 80 and SBE-β-CD where applicable. The CD33_2-hALB target concentration was 5.0 mg/mL. The finally formulated bulks were filled into prewashed and presterilized type I glass vials. Vials were stoppered with sterilized butyl rubber stoppers and were sealed with aluminum caps. The fill volume totaled 1.0 mL. An overview on formulations is provided by Table 3. The vials were stored for six days in a temperature controlled cabinet at 37° C. High molecular weight species were quantified by SE-UPLC using the method described under Example 1. The injected amount of protein totaled 3 μg.

TABLE 3

Overview on CD33_2-hALB formulations

ID	Citric acid	Potassium phosphate	Sucrose	SBE-β-CD	Polysorbate	80	pH

C50SuT

	20 mM		6% w/V		0.01% w/V	5.0
C50SBESuT	20 mM		6% w/V	1% w/V	0.01% w/V	5.0
K60SuT		20 mM	6% w/V		0.01% w/V	6.0
K60SBESuT		20 mM	6% w/V	1% w/V	0.01% w/V	6.0
K70SuT		20 mM	6% w/V		0.01% w/V	7.0
K70SBESuT		20 mM	6% w/V	1% w/V	0.01% w/V	7.0

Formulations containing SBE-β-CD (F2, F4, F6) showed lower amounts of high molecular weight species (HMWS) after incubation if compared to cyclodextrin free preparations. The effect was more pronounced at pH 6 and 7 than at pH 5 (FIG. 6 ).

Example 6: Effect of Ultrafiltration and Diafiltration on Formulations Comprising Bispecific Antibody Constructs and β-CD

Purified MSLN-hALB (i.e., SEQ ID NO: 176) was concentrated stepwise by ultrafiltration (UF). First a seven fold concentration was performed using a cassette equipped with a regenerated cellulose membrane and surface of 0.11 m². A further seven fold concentration was carried out with a smaller membrane with a surface of 50 cm². Both membranes had a molecular weight cut-off (MWCO) of 10 kDa. For ultrafiltration and diafiltration steps the transmembrane pressure was limited to 1.4 bar. The concentrated pool was divided into two parts. The first part was dialfiltrated into a buffer composed of 20 mM potassium phosphate, 150 mM L-arginine hydrochloride, 6% (w/V) trehalose dihydrate at pH 6.0. The second part was diafiltrated into a buffer composed of 20 mM potassium phosphate, 2% (w/V) Sucrose at pH 6.0. The final formulations listed in Table 4 were adjusted by adding concentrated stock solutions to the diafiltrated materials. All excipients were applied in compendial grade. The target MSLN-hALB concentration was 1.0 mg/mL.

TABLE 4

Overview on MSLN-hALB formulations

ID	Formulation composition

K60RTrT-low	20 mM potassium phosphate, 150 mM L-arginine HCl, 6% (w/V) trehalose
	dihydrate, 0.01.% (w/V) polysorbate 80, pH 6.0
K60SBESuT-low	20 mM potassium phosphate, 1% (w/V) SBE-β-CD, 8% (w/V) Sucrose,
	0.01% (w/V) polysorbate 80, pH 6.0
K60RMSuT-low	20 mM potassium phosphate, 150 mM L-arginine HCl, 4% (w/V) mannitol,
	2% (w/V) sucrose, 0.01.% (w/V) polysorbate 80, pH 6.0

Finally MSLN-hALB drug substance was sterile filtered through a 0.2 μm PVDF filter and filled into prewashed and presterilized type I glass vials. Vials were stoppered with sterilized butyl rubber stoppers and were sealed with aluminum caps. The fill volume totaled 1.0 mL. The vials were stored for up to two weeks in temperature controlled cabinets at 25° C. and 37° C. respectively. High molecular weight species were quantified by SE-UPLC using the method described under Example 1. The injected amount of protein totaled 3 μg. Acidic charge variants were determined using weak cation exchange ultra high performance liquid chromatography (WCX-UPLC). WCX-UPLC was performed on a UPLC H class Aquity (Waters) using a Protein-Pak Hi Res CM 7 μm 4.6×100 mm column. The column temperature was set to 30° C. In order to achieve chromatographic separation the following gradient (Table 5) was applied:

TABLE 5

Overview on WCX-UPLC gradient

Time [min:sec]	% Eluent A	% Eluent B

0:00	100	0
4:00	100	0
25:00	50	50
25.01	0	100
29:00	0	100
29:01	100	0
33:00	100	0

Eluent A was composed of 20 mM sodium phosphate at pH 6.5. Eluent B was composed of 20 mM sodium phosphate, 250 mM sodium chloride, pH 6.5. The injected amount of protein totaled 3 μg. The flow rate was 0.65 mL/min. Prior to injection, samples were held in the autosampler at 8° C. Protein detection relied on the measurement of intrinsic fluorescence intensity. Excitation was performed at 280 nm and emission was taken at 330 nm. Acidic charge variants were quantified based on the relative area under the curve (AUC). Integration was performed using Empower® software.
The lowest high molecular weight species (HMWS) formation rates were observed for the formulation with SBE-β-CD (FIG. 7B). The chemical stability was also most pronounced for the SBE-β-CD containing formulation indicated by the lowest fraction of acidic charge variants (FIG. 8 ).

Example 7: LLPS of AMG 330 with SBE-β-CD and Alginate

LLPS: Liquid-Liquid Phase Separation (LLPS) is caused by net attraction between the colloidal particles (e.g. proteins) and thus is measure of strength of this attraction. When there is attraction between proteins, a LLPS occurs into coexisting protein-rich and protein-poor phases, provided the temperature is sufficiently low. In LLPS, the co-existing phases are in true thermodynamic equilibrium and are fully reversible and the concentrations of the coexisting phases depend only on temperature and not on the initial protein concentration. LLPS can be induced by addition of PEG. If there is a stronger the attraction between proteins, the lower the PEG concentration that is necessary for LLPS to occur, which in turn indicates that these proteins will easily aggregate. At a given temperature and PEG concentration, excipients that increase colloidal stability of a protein result in a higher protein concentration in protein-poor phase. This increase in protein concentration can be measured chromatographically relative to a control without an excipient. In formulation development it is desirable to observe LLPS and evaluate the attraction between protein molecules.
The purpose of this experiment is to use LLPS to evaluate the effect of SBE-β-CD and Alginate on the colloidal stability of AMG 330.

TABLE 6

Solution composition and preparation:

Solution
ID	Solution Composition	Solution Preparation	Volume

A	AMG 330 (1.2 mg/ml)	n/a	180 uL needed
B	1X PBS		5 mL 10X PBS + 45 mL	50 mL
		milli Q water
C
	50% SBE-β-CD in 1X PBS (pH to	5 g in 10 g
	match 1x PBS)
D	1% SBE-β-CD in 1X PBS	100 uL C + 4.9 mL B	5 mL
E	0.1% SBE-β-CD in 1X PBS	10 uL + 4.99 mL B	5 mL
F
	1% Alginate in 1x PBS (pH to	0.2 g in 20 g
	match
1X PBS)
G	0.1% Alginate in 1x PBS	500 uL F + 4.5 mL B	5 mL
H
	24% PEG 3350 IN 1X PBS	4.8 g in 20 g

TABLE 7

Sample composition and preparation:

			Final
Sample			volume
ID	Sample Composition	Sample preparation	(uL)

1-1	AMG 330 + 1X PBS, 0% PEG	(10 uL A + 40 uL B) + 50 uL B	100
1-2	AMG 330 + 1X PBS, 0% PEG	(10 uL A + 40 uL B) + 50 uL B	100
2-1	AMG 330 + 1X PBS, 12% PEG	(10 uL A + 40 uL B) + 50 uL H	100
2-2	AMG 330 + 1X PBS, 12% PEG	(10 uL A + 40 uL B) + 50 uL H	100
3-1	AMG 330 + 0.001% SBE-β-CD, 12%	(10 uL A + 1 uL E + 39 uL B) + 50	100
	PEG	uL H
3-2	AMG 330 + 0.001% SBE-β-CD, 12%	(10 uL A + 1 uL E + 39 uL B) + 50	100
	PEG	uL H
4-1	AMG 330 + 0.01% SBE-β-CD, 12% PEG	(10 uL A + 1 uL D + 39 uL B) + 50	100
		uL H
4-2	AMG 330 + 0.01% SBE-β-CD, 12% PEG	(10 uL A + 1 uL D + 39 uL B) + 50	100
		uL H
5-1	AMG 330 + 0.1% SBE-β-CD, 12% PEG	(10 uL A + 10 uL D + 30 uL B) +	100
		50 uL H
5-2	AMG 330 + 0.1% SBE-β-CD, 12% PEG	(10 uL A + 10 uL D + 30 uL B) +	100
		50 uL H
6-1	AMG 330 + 1% SBE-β-CD, 12% PEG	(10 uL A + 2 uL C + 38 uL B) + 50	100
		uL H
6-2	AMG 330 + 1% SBE-β-CD, 12% PEG	(10 uL A + 2 uL C + 38 uL B) + 50	100
		uL H
7-1	AMG 330 + 0.001% Alginate, 12% PEG	(10 uL A + 1 uL G + 39 uL B) + 50	100
		uL H
7-2	AMG 330 + 0.001% Alginate, 12% PEG	(10 uL A + 1 uL G + 39 uL B) + 50	100
		uL H
8-1	AMG 330 + 0.01% Alginate, 12% PEG	(10 uL A + 1 uL F + 39 uL B) + 50	100
		uL H
8-2	AMG 330 + 0.01% Alginate, 12% PEG	(10 uL A + 1 uL F + 39 uL B) + 50	100
		uL H
9-1	AMG 330 + 0.1% Alginate, 12% PEG	(10 uL A + 10 uL F + 30 uL B) +	100
		50 uL H
9-2	AMG 330 + 0.1% Alginate, 12% PEG	(10 uL A + 10 uL F + 30 uL B) +	100
		50 uL H

Different solution/sample composition and preparation was prepared as mentioned in the table 6 and 7 above. Samples were prepared (final AMG 330 concentration of 0.12 mg/ml) and incubated at 40° C. for three days. Samples were then micro centrifuged (Eppendorf Centrifuge 5418, St. Louis, Mo., USA) for 20 sec and 80 uL supernatant was removed and analyzed by analytical CEX (ProPac WCX-10 column, 2 mm ID) in Agilent chromatography system (Agilent 1200, Santa Clara, Calif., USA).
Analytical CEX: 70 μL of the sample were injected into the CEX column which was equilibrated with 20 mM Citric acid, 0.005% Sodium Azide, pH 6.0 and eluted with 20 mM Citric acid, 1M Sodium Chloride, 0.005% Sodium Azide pH 6.0, with a gradient time of 30 min (total run time: 45 min/injection) with a maximum concentration of 500 mM Sodium chloride at a flow rate of 0.2 mL/min. Autosampler temperature were maintained at 40 C during the run. From the chromatograms, peak areas of the samples were calculated (FIGS. 9 and 10 ).

Example 8: Buffer Exchange and Protein Concentration of AMG 330 by Ultrafiltration Centrifugation in the Presence of 4 Different Formulations (Including SBE-β-CD)

TABLE 8

Solution composition and preparation (Volume in mL):

Solution ID	Solution composition	Solution preparation	Vol to prepare

A	0.4 mg/mL AMG 330	N/A	17 mL
B
	10 mM Citrate, pH 6.0		N/A
C
	40% Captisol in 1X PBS
D	500 mM Arg, 500 mM Glu in B, pH 6.0
E	35 mM Tris, 17.5 mM Na phosphate, 50 mM
	Arg, 1.4% Trehalose, pH 6.0
F	65% Sucrose (w/v) in B
G	18% Mannitol (w/v) in B
H	1% Polysorbate 80 (w/v) in B
I	1% PEG 4000 (w/w) in E, pH 6.0
J	10 mM Citrate pH 6.0, 3% Captisol	97.5 mL B + 2.5 mL C	100 mL
K	3.5 mM Tris, 17.5 mM Na phosphate, 0 mM	95 mL + 5 mL I
	Arg, 1.4% Trehalose, 0 % PEG 4000, pH 6.0
L	10 mM Citrate, 50 mM Arg, 50 mM Glu, 2%	63.8 mL B + 10 mL + 3.1 mL +
	Sucrose, 4% Mannitol, 0.01% PS-80, pH 6.0	22.2 mL G + 1 mL H

indicates data missing or illegible when filed

TABLE 9

Sample composition and preparation:

Sample ID	Sample composition	Sample preparation

1-1	AMG 330 in 10 mM Citrate, pH 6.0	2 mL A, buffer exchange in by centrifugation/filtration
1-2
2-1	AMG 330 in 10 mM Citrate, pH , 1% Captisol	2 mL A, buffer exchange in J by centrifugation/filtration
2-2
3-1	AMG 330 in 5 mM Tris, 17.5 mM Na phosphate,	2 mL A, buffer exchange in K by centrifugation/filtration
	50 mM Arg, 1.4% Trehalose, 0.05% PEG-4000,
	pH 6.0
3-2
4-1	AMG 330 in 10 mM Citrate, 50 mM Arg, 50 mM	2 mL A, buffer exchange in L by centrifugation/filtration
	Glu, 2% Sucrose, 4% Mannitol, 0.01% PS-80,
	pH 6.0
4-2
5-1	AMG 330, no buffer exchange	10 uL A into HPLC
5-2

indicates data missing or illegible when filed

Initial protein concentration was 0.4 mg/ml. 2 mL of 0.4 mg/ml AMG 330 were placed into an Amicon ultra 15 ml centrifugal filter, MWCO 10,000. 10 mL of the appropriate buffer were added to each tube and gently mixed with protein and centrifuged (Allegra 6R Centrifuge, Beckman Coulter, Brea, Calif., USA) for 3 hrs at 2000 rpm at 4° C. The retentate was then gently mixed and the tubes were centrifuged for 1.5 hrs at 2500 rpm at 25° C. Following a retentate volume of 200-250 μL, 10 mL of appropriate buffer was added to each and gently mixed with the retentate and then centrifuged for 30 min at 2500 rpm at 25° C. to a final volume of 200-250 μL. Final protein concentration in 4 different formulations ranged from 2.9 to 3.7 mg/ml.
Analytical SEC: Samples were analyzed by analytical SEC (TSKgel G3000SWXL, 7.8 mm ID, PA, USA) in an Agilent chromatography system (Agilent 1200, Santa Clara, Calif., USA) with a running buffer of 100 mM sodium phosphate, 250 mM Sodium chloride, pH 6.8 with a flow rate of 0.5 mL/min (total run time: 35 min/injection). Autosampler temperature was maintained at 4° C. during the run.
The presence of SBE-β-CD appears to provide significant protection to AMG 330 against the formation of HMW during protein concentration by ultrafiltration with the lowest relative amount of aggregates in formulation containing SBE-β-CD. The formulation containing Arginine, Glutamate, Sucrose, Mannitol and PS-80 had the highest amount of HMW followed by the formulation containing Tris, phosphate, Arginine, Trehalose and PEG 4000 (FIG. 11 ). CEX analysis showed similar effect (data not shown).

Example 9: Small Scale Formulation Study of AMG 330 Including SBE-β-CD (LLPS, FT, UFC)

The purpose of this experiment is to evaluate the stability of AMG 330 after various stresses in 14 different formulations. Specifically, AMG 330 was evaluated after LLPS, 20 freeze/thaw (F/T) cycles and concentration by ultrafiltration/centrifugation (UFC). As shown in Example 8, SBE-β-CD provides protection against AMG 330 aggregation and is further evaluated in this experiment. For UFC (FIG. 12A, FIG. 12B), only 5 formulations were investigated. For LLPS and F/T studies (FIG. 12C, FIG. 12D), 14 formulations were investigated. LLPS samples were analyzed by analytical CEX, whereas UFC and F/T samples were analyzed by both analytical SEC and CEX.

Materials and Methods:

TABLE 10

Stock solution preparation:

Solution ID	Solution composition	Solution preparation	volume

A
	20 mM Citrate, pH 6.0	by media prep	20 L
B	2 mg/mL AMG 330,	dialysis of 0.4 mg/mL AMG 330, then	20 mL, concentrate
	buffer exchange in A	concentration by ultrafiltration/centrifugation	to mL
C	% polysorbate 80 (w/w) in A	2 g, bring to 100 g in A	100 mL
D
	10% SBE-β-CD (w/w) in A, pH 6.0	g, bring to 50 g in A, pH adjust to 6.0	50 mL
E
	15% Glycine in (w/w) A, pH 6.0	7.5 g, bring to 50 g in A, pH adjust to 6.0
F	40% Sucrose (w/w) in A	20 g, bring to 25 g in A	25 mL
G
	1 % Mannitol (w/w) in A	3.5 g, bring to 25 g in A
H	400 mM Arg in A, pH 6.0	3.484 g Arg, bring to 50 mL in A, pH adjust	50 mL
		to 6.0
I	200 mM Arg, 200 mM Glu in A, pH 6.0	1.742 g Arg + 1.47 g Glu, bring to 50 mL
		in A, pH adjust to 6.0
J	1 % Trehalose dihydrate (w/w)in A	.75 g, bring to 25 g in A	25 mL
K
	200 PEG 3350 (w/w) in A, pH 6.0	3 .4 g, bring to 40 g in A, pH adjust to 6.0	40 mL
L
	1. mg/mL AMG 330 + 0.074% PS80	2100 uL B + 108 uL C	2 uL
M
	40% SBE-β-CD (w/w) in A, pH 6.0	6 g, bring to 15 g in A, pH adjuct to 6.0	3.5 mL
N	% Sucrose (w/w) in A	5 g, bring to 25 g in A	2 mL

indicates data missing or illegible when filed

Ultrafiltration/Centrifugation (UFC):

TABLE 11

Sample composition preparation for UFC (Volume in μL).

20mM Cit

PS-80

Captisol

Glycine

Sucrose

Sample ID	Sample composition	A	C	D	E	F

2-1_UFC	control	79.2	0.8
3-1_UFC	0.5% SBE-β-CD	75.2	0.8	4
4-1_UFC	1% SBE-β-CD	71.2	0.8	8
5-1_UFC	2% SBE-β-CD	63.2	0.8	16
6-1_UFC	2% SBE-β-CD, 2% Glycine, 1% Sucrose	58.5	0.8	9	10.7	2
8-1_UFC	2% Glycine, 1% Sucrose	66.5	0.8		10.7	2

For each sample, 4 mL of 0.4 mg/mL AMG 330 were placed into an Amicon Ultra 15 ml centrifugal filter tube of MWCO 10,000. 8 mL of the appropriate buffer were added to each tube and gently mixed with protein and centrifuged (Allegra 6R Centrifuge, Beckman Coulter, Brea, Calif., USA) at 2000 rpm (4000 rcf) at 20° C. until the retentate volume was 200-250 uL. This process were repeated twice more for a total of 3 concentration steps. The retentate was then gently mixed with a pipettor removed from the filter tube, placed in an Eppendorf tube and micro-centrifuged (Eppendorf Centrifuge 5418, St. Louis, Mo., USA) at maximum speed for 2 min. Following this, protein concentration was measured for the supernatant, and analyzed by analytical SEC (same details as in Example 8) by injecting 20 μL. Each sample was prepared in duplicate.

LLPS:

Samples were prepared as outlined in table below and incubated for 5 days at 4° C. The final volume of all the samples was 240 μL. After incubation, samples were micro centrifuged (Eppendorf Centrifuge 5418, St. Louis, Mo., USA) for 20 s, then 200 μL supernatant was removed for analytical CEX (same details as in Example 7), except the autosampler temperature was maintained at 25° C.

TABLE 12

Sample composition preparation for LLPS:

	20 mM	AMG	40%
	Citrate,	330	SBE					Arginine
	pH	+	-β-		55%			+
Volume in uL	6.0	PS80	CD	Glycine	Sucrose	Mannitol	Arginine	Glutamate	Trehalose	PEG

ID	Sample composition	A	L	M	E	N	G	H	I	J	K

1	Control, 0% PEG	207.6	32.4								0
2	Control, 13% PEG	87.6	32.4								0
3	0.5% SBE-β-CD, 13% PEG	84.6	32.4	3							120
4	1% SBE-β-CD, 13% PEG	81.6	32.4	6							120
5	2% SBE-β-CD, 13% PEG	75.6	32.4	12							120
6	1% SBE-β-CD, 1%	45.2	32.4	6	32	4.4					120
	Glycine, 1% Sucrose,
	13% PEG
7	4% Glycine, 13% PEG	23.6	32.4		64						120
8	2% Glycine, 1%	51.2	32.4		32	4.4					120
	Sucrose, 13% PEG
9	4% Mannitol, 13% PEG	19	32.4				68.6				120
10	100 mM Arginine, 13% PEG	27.6	32.4					60			120
11	50 mM Arginine, 50	27.6	32.4						60		120
	mM Glutamate, 13% PEG
12	4% Sucrose, 13% PEG	70.1	32.4			17.5					120
13	4% Trehalose	23.6	32.4							64	120
	dehydrate, 13% PEG
14	1% SBE-β-CD, 4%	64.1	32.4	6		17.5					120
	Sucrose, 13% PEG
15	1% SBE-β-CD, 4%	4.3	32.4	6		8.7	68.6				120
	Mannitol, 2% Sucrose,
	13% PEG

Increasing concentrations of SBE-β-CD resulted in increased monomer recovery while maintaining relatively low level of aggregates. SBE-β-CD performed even better when in combination with sucrose, mannitol and sucrose, and especially with glycine and sucrose. This is especially striking because Glycine alone performed quite poorly and it didn't do much better in combination with sucrose.

Freeze/Thaw (F/T):

TABLE 13

Sample composition preparation for F/T:

	20 mM	AMG	40%				Arginine
	Citrate,	330 +	SBE-		55%		+
Volume in uL	pH 6.0	PS80	β-CD	Glycine	Sucrose	Mannitol	Glutamate	Trehalose

ID	Sample composition	A	L	M	E	N	G	I	J

1	Control, −70 C.	207.6	32.4
2	Control, −30 C.	207.6	32.4
3	0.5% SBE-β-CD, −70 C.	204.6	32.4	3
4	0.5% SBE-β-CD, −30 C.	204.6	32.4	3
5	1% SBE-β-CD, −70 C.	201.6	32.4	6
6	1% SBE-β-CD, −30 C.	201.6	32.4	6
7	2% SBE-β-CD, −70 C.	195.6	32.4	12
8	2% SBE-β-CD, −30 C.	195.6	32.4	12
9	1% SBE-β-CD, 2%	165.2	32.4	6	32	4.4
	Glycine, 1%
	Sucrose, −70 C.
10	1% SBE-β-CD, 2%	165.2	32.4	6	32	4.4
	Glycine, 1%
	Sucrose,−30 C.
11	4% Glycine, −70 C.	143.6	32.4		64
12	4% Glycine, −30 C.	143.6	32.4		64
13	2% Glycine, 1%	171.2	32.4		32	4.4
	Sucrose, −70 C.
14	2% Glycine, 1%	171.2	32.4		32	4.4
	Sucrose, −30 C.
15	4% Mannitol, −70 C.	139	32.4				68.6
16	4% Mannitol, −30 C.	139	32.4				68.6
17	50 mM Arginine, 50	147.6	32.4					60
	mM Glutamate, −70 C.
18	50 mM Arginine, 50	147.6	32.4					60
	mM Glutamate, −30 C.
19	4% Trehalose	143.6	32.4						64
	dehydrate, −70 C.
20	4% Trehalose	143.6	32.4						64
	dehydrate, −30 C.
21	1% SBE-β-CD, 4%	184.1	32.4	6		17.5
	Sucrose, -70 C.
22	1% SBE-β-CD, 4%	184.1	32.4	6		17.5
	Sucrose, -30 C.
23	1% SBE-β-CD, 4%	124.3	32.4	6		8.7	68.6
	Mannitol, 2%
	Sucrose, −70 C.
24	1% SBE-β-CD, 4%	124.3	32.4	6		8.7	68.6
	Mannitol, 2%
	Sucrose, −30 C.

Samples were prepared as tabulated above. 20 F/T cycles were performed, with samples stored for at least on hour at −70° C. or −30° C. during each freeze, and at room temperature for no more than one hour during thaw. Final volume of each sample was 240 μL. Aliquots were removed for analytical SEC (same as Example 8) analysis after 0 and 20 cycles.
The presence of SBE-β-CD appears to provide benefit toward reducing aggregation and increasing relative monomer levels during F/T in comparison to other formulations. The formulations in which SBE-β-CD was used in combination with other excipients also performed well, particularly with Glycine and Sucrose.

Example 10: Comparing the Effects of SBE-β-CD and 2-Hydroxypropyl Beta-Cyclodextrin

SBE-β-CD has been shown in previous UFC experiment to provide significant protection to AMG 330 against aggregation during protein concentration. In the present experiment, the effects on AMG 330 during protein concentration by UFC are compared in the presence of either SBE-β-CD or another cyclodextrin, 2-Hydroxypropyl beta-cyclodextrin (2-HP-β-CD).

Materials and Methods:

20 mL of 0.4 mg/mL AMG 330 were concentrated to ˜10 mL in Amicon Ultra 15 mL centrifugal filter tubes of MWCO 10,000. The retentate of the tubes were combined, and the concentration of the protein was then measured by SoloVPE (using extinction coefficient of 2.319 mL/(mg*cm)) and found to be 0.83 mg/mL. This protein was then used to prepare the UFC samples.
All samples contained 10 mM Potassium phosphate, 8% sucrose, 0.01% Polysorbate-80, pH 6.0.
Five formulation conditions were tested: 1) control with buffer only, 2) 1% SBE-β-CD added, 3) 2% SBE-β-CD added, 4) 1% 2-HP-β-CD added, and 5) 2% 2-HP-β-CD added. 50 mL of each of the 5 buffer solutions were prepared. Two replicate samples of each formulation were tested.
For each sample, 0.875 mL of AMG 330 was placed into an Amicon Ultra 4 mL centrifugal filter tube of MWCO 10,000. 3.125 mL of the appropriate buffer were added to each tube and mixed gently with the protein, and the tubes were centrifuged (Allegra 6R Centrifuge, Beckman Coulter, Brea, Calif., USA) at 4000 rcf at 25 C until retentate volume was ˜100 uL. 4 mL additional buffer was added, and the samples were again concentrated to ˜100 uL. There tentate was then gently mixed with a pipettor, and 45 uL were removed from the filter tube, placed in an Eppendorf tube, and micro-centrifuged (Eppendorf Centrifuge 5418, St. Louis, Mo., USA) at maximum speed for 2 min. The supernatant was analyzed by analytical SEC (same as Example 8). Non-concentrated AMG 330 (0.4 mg/mL) was also analyzed for comparison purposes.
In this experiment, AMG 330 was concentrated up to ˜10 mg/mL in the presence of 1 and 2% SBE-β-CD or 2-HP-β-CD. The SBE-β-CD containing formulations are indicated by asterisks. The control on the left (labeled as 0.4 mg/mL) was not concentrated beyond it starting concentration of 0.4 mg/mL. Second from the left (labeled as Control in FIG. 4A and FIG. 4B) is sample that was concentrated without any cyclodextrin. The comparison between SBE-β-CD and 2-HP-β-CD formulations demonstrated the advantage of using SBE-β-CD. FIG. 13 shows the highest concentration reached; FIG. 14 reveals the composition of these concentrated solutions in terms of % aggregate and % monomer.

Example 11: Comparing the Effects of Four Different Cyclodextrins for their Ability to Maintain AMG 330 in a Soluble Non-Aggregated Form

SBE-β-CD has been shown to reduce aggregation in AMG 330 in previous experiments. The purpose of this experiment is to evaluate other cyclodextrins in comparison to SBE-β-CD. The levels of aggregation in AMG 330 were measured after 1-4 days incubation at 4° C. and 25° C. with 4 different cyclodextrins.

Materials and Methods:

All samples also contained ˜2 mg/ mL AMG 330, 20 mM Citrate, and 0.01% Polysorbate-80, pH 6.0. Samples were prepared and stored in Eppendorf tubes (table 14). The tubes were wrapped in plastic and protected from light during incubation. Aliquots were taken after 1 and 4 days incubation at 4° C. and 25° C. (Thermofisher Scientific, (Newington, N.H.) Haake A28). The aliquots were briefly micro centrifuged (Eppendorf Centrifuge 5418, St. Louis, Mo., USA) and the supernatants were analyzed by analytical SEC.

TABLE 14

Solution composition and preparation:

Solution		Solution
ID	Solution composition	preparation	Volume

A
	2 mg/mL AMG 330	N/A	500 uL
B
	20 mM Citrate, pH 6.0	N/A
C
	10% SBE-β-CD in B	1.0 g, bring to 10 g in B
D
	10% alpha-cyclodextrin	1.0 g, bring to 10 g in B	10 mL
	(α-CD) in B
E
	10% gamma-cyclodextrin	1.0 g, bring to 10 g in B	10 mL
	(γ-CD) in B
F
	10% 2-hydroxypropyl-	1.0 g, bring to 10 g in B	10 mL
	beta-cyclodextrin (2-
	HP-β-CD) in B
G
	1% PS-80 in B	N/A
H
	2 mg/mL AMG 330 +	495 uL A + 5 uL G	500 uL
	0.01% PS-80

TABLE 15

Sample composition and preparation:

					Storage
	Sample	Sample		Aliquot	temperature
Sample ID	composition	preparation	Volume	Volume	(C.)

Control at 4° C.	Control	95 uL H + 5 uL B	100 uL	50	4 C. (Fridge)
				uL
Control at 25° C.	Control	95 uL H + 5 uL B	100 uL	50	25 C.
				uL	(Incubator)
0.5% SBE-β-CD at 4° C.	0.5% SBE-β-CD	95 uL H + 5 uL C	100 uL	50	4 C. (Fridge)
				uL
0.5% SBE-β-CD at 25° C.	0.5% SBE-β-CD	95 uL H + 5 uL C	100 uL	50	25 C.
				uL	(Incubator)
0.5% α-CD at 4° C.	0.5% α-CD	95 uL H + 5 uL D	100 uL	50	4 C. (Fridge)
				uL
0.5% α-CD at 25° C.	0.5% α-CD	95 uL H + 5 uL D	100 uL	50	25 C.
				uL	(Incubator)
0.5% γ-CD at 4° C.	0.5% γ-CD	95 uL H + 5 uL E	100 uL	50	4 C. (Fridge)
				uL
0.5% γ-CD at 25° C.	0.5% γ-CD	95 uL H + 5 uL E	100 uL	50	25 C.
				uL	(Incubator)
0.5% 2-HP-β-CD at 4° C.	0.5% 2-HP-β-CD	95 uL H + 5 uL F	100 uL	50	4 C. (Fridge)
				uL
0.5% 2-HP-β-CD at 25° C.	0.5% 2-HP-β-CD	95 uL H + 5 uL F	100 uL	50	25 C.
				uL	(Incubator)

Four different cyclodextrins, including SBE-β-CD, were tested for ability to maintain AMG 330 in a soluble non-aggregated form. Protein at ˜2 mg/ml was incubated for 4 days at 4° and 25° C. without further concentration. All samples also contained 20 mM Citrate and 0.01% Polysorbate-80, pH 6.0.
At end of 4 days at 4° C., 0.5% SBE-β-CD formulation had a larger total peak area by SEC indicating higher soluble protein concentrations. Other formulations precipitated and aggregated to various degrees. This result demonstrate that SBE-β-CD was a more effective stabilizer and solubilizer of AMG 330 at both temperatures (4° and 25° C.) compared to α-cyclodextrin, γ-cyclodextrin or hydroxypropyl R-cyclodextrins seemed to fare better only at 25° C. (FIG. 15 ).

Example 12: AMG 330 in 13 Different Formulations at 1 mg/mL and Stored at ˜20, ˜30 and ˜70° C. for Up to 6 Weeks

The purpose of this experiment is to develop a stable frozen and lyophilized formulation for AMG 330 SBE-β-CD and Triton X-100 was evaluated s formulation excipients. Polycarbonate carboys will be used to simulate drug substance (DS) frozen storage.

Materials and Methods:

With a starting concentration of 0.4 mg/mL for AMG 330, UF/F buffer exchange (buffers listed in table 16) was carried out using two cogent μScale TFF systems with a delta pressure set at 23 psi. Four Millipore Pellicon 3 Ultracel 10 kD 0.11 m2 cassettes and two cogent tubing assemblies were used. Post exchange, the material was over-concentrated to 1.2 mg/mL and collected in sterile Nalgene containers.

TABLE 16

Formulation composition:

Sample	Formulation
ID	Abbreviation	Formulation composition

FRM 1	C60CpGSuP	10 mM Citrate, 1% SBE-β-CD, 2% Glycine, 1% Sucrose, 0.01%
		PS80, pH 6.0
FRM 2	C60CpMSuP	10 mM Citrate, 1% SBE-β-CD, 4% Mannitol, 2% Sucrose, 0.01%
		PS80, pH 6.0
FRM 3	C60CpSuP	10 mM Citrate, 1% SBE-β-CD, 8% Sucrose, 0.01% PS80, pH 6.0
FRM 4	H60CpGSuP	10 mM Histidine, 1% SBE-β-CD, 2% Glycine, 1% Sucrose, 0.01%
		PS80, pH 6.0
FRM 5	H60CpMSuP	10 mM Histidine, 1% SBE-β-CD, 4% Mannitol, 2% Sucrose, 0.01%
		PS80, pH 6.0
FRM 6	H60CpSuP	10 mM Histidine, 1% SBE-β-CD, 8% Sucrose, 0.01% PS80, pH 6.0
FRM 7	KP60CpGSuP	10 mM Potassium phosphate, 1% SBE-β-CD, 2% Glycine, 1%
		Sucrose, 0.01% PS80, pH 6.0
FRM 8	KP60CpMSuP	10 mM Potassium phosphate, 1% SBE-β-CD, 4% Mannitol, 2%
		Sucrose, 0.01% PS80, pH 6.0
FRM 9	KP60CpSuP	10 mM Potassium phosphate, 1% SBE-β-CD, 8% Sucrose, 0.01%
		PS80, pH 6.0
FRM 10	KP60CpGSuT	10 mM Potassium phosphate, 1% SBE-β-CD, 2% Glycine, 1%
		Sucrose, 0.004% Triton X-100, pH 6.0
FRM 11	KP60CpMSuT	10 mM Potassium phosphate, 1% SBE-β-CD, 4% Mannitol, 2%
		Sucrose, 0.004% Triton X-100, pH 6.0
FRM 12	KP60CpSuT	10 mM Potassium phosphate, 1% SBE-β-CD, 8% Sucrose, 0.004%
		Triton X-100, pH 6.0
FRM 13	PEG 4000	35 mM Tris, 17.5 mM Sodium phosphate, 50 mM Arginine, 1.4%
		Trehalose, 0.05% PEG 4000 at pH 6.0

Formulation buffer, PEG and surfactant stocks were freshly prepared and added to produce the final formulated material. Samples were filled out at a volume of 15 mL in 30 mL PC carboys (Nalgene) for this experiment). All samples were filtered in a sterile hood using sterivex filter units (0.22 μm) prior to filling. Final protein concentration in PC carboys is 1 mg/mL.
For static experiments, samples were measured by analytical SEC (same as Example 8) at t=0 and t=6 weeks.

Results:

SBE-β-CD was included in AMG 330 formulations that were incubated at various temperatures. Results after 6 weeks of storage showed that all the SBE-β-CD containing formulations were stable in contrast to a formulation based on the use of PEG-4000 and without SBE-β-CD.
The comparison between SBE-β-CD and PEG based formulation demonstrates the advantage of using SBE-β-CD. PEG based formulation aggregated and particulated heavily after storage at −20° C. (FIG. 16 ).

Example 13: Evaluation of Two Cyclodextrans (SBE-β-CD and α-Cyclodextrin) as Excipients for Lyophilized Formulation for AMG 330

This experiment was conducted to determine a platform lyophilized formulation can be developed for BiTE® molecules. AMG 330 BiTE® was used as a model protein. Two cyclodextrins (SBE-β-CD and α-cyclodextran) was evaluated as formulation excipients.

Materials and Methods:

AMG 330 drug substance concentration is 0.4 mg/mL. AMG 330 was buffer exchanged into respective buffers (listed in table 17) using Millipore Centripreps (30K NMWL, 15 mL):
1. Aliquoted 30 mL of AMG 330 DS into two (2×15 mL) Centriprep sample containers per formulation
2. Added 4.4 mL of corresponding formulation buffer to each Centriprep filtrate collector (to prevent overconcentration of DS)
3. Centrifuged (Allegra 6R Centrifuge, Beckman Coulter, Brea, Calif., USA) at 1500×g for 20 min at 25° C. (centrifuged to equilibrium); ˜ 5 mL of protein remaining in each sample container, 3-fold concentration to 1.2 mg/mL target
4. Decanted filtrate in each filtrate collector and replaced with 4.4 mL of fresh formulation buffer; added 10 mL of fresh formulation buffer to each sample container
5. Centrifuged per step 3
6. Repeated steps 4-5 four more times (five buffer exchanges total; ˜243-fold total dilution)
7. Stored buffer-exchanged material O/N at 4° C.

TABLE 17

Formulation components for lyophilization:

	Formulation
	concentration
Sample ID	(mg/mL)	Buffer	Excipient	Surfactant	pH

C60SuT	0.85	20 mM	4% (w/v)	0.01% (w/V)	6
		Citrate	Sucrose	Polysorbate
				80
C60GSuT	0.85	20 mM	2% (w/v)	0.01% (w/V)	6
		Citrate	Glycine, 1%	Polysorbate
			(w/v)	80
			Sucrose
C60MSuT	0.85	20 mM	4%	0.01% (w/V)	6
		Citrate	Mannitol,	Polysorbate
			2% (w/v)	80
			Sucrose
C60RSuT	0.85	20 mM	75 mM	0.01% (w/V)	6
		Citrate	Arginine, 4%	Polysorbate
			(w/v)	80
			Sucrose
C60CpT	0.85	20 mM	0.5% (w/v)	0.01% (w/V)	6
		Citrate	SBE-β-CD	Polysorbate
				80
C60CpSuT	0.85	20 mM	0.5% (w/v)	0.01% (w/V)	6
		Citrate	SBE-β-CD,	Polysorbate
			4% (w/v)	80
			Sucrose
C60CpGSuT	0.85	20 mM	0.5% (w/v)	0.01% (w/V)	6
		Citrate	SBE-β-CD,	Polysorbate
			2% (w/v)	80
			Glycine, 1%
			(w/v)
			Sucrose
C60CpMSuT	0.85	20 mM	0.5% (w/v)	0.01% (w/V)	6
		Citrate	SBE-β-CD,	Polysorbate
			4% (w/v)	80
			Mannitol,
			2% (w/v)
			Sucrose
C60AcL	0.85	20 mM	0.5% (w/v) α-	0.01% (w/V)	6
		Citrate	Cyclodextrin	Lutrol F68
C60AcSuL	0.85	20 mM	0.5% (w/v) α-	0.01% (w/V)	6
		Citrate	Cyclodextrin,	Lutrol F68
			4% (w/v)
			Sucrose
C60AcGSuL	0.85	20 mM	0.5% (w/v) α-	0.01% (w/V)	6
		Citrate	Cyclodextrin,	Lutrol F68
			2% (w/v)
			Glycine, 1%
			(w/v)
			Sucrose
C60AcMSuL	0.85	20 mM	0.5% (w/v) α-	0.01% (w/V)	6
		Citrate	Cyclodextrin,	Lutrol F68
			4% (w/v)
			Mannitol,
			2% (w/v)
			Sucrose

Formulation buffer and surfactant stocks were added to produce the final formulated material. Samples were filled at a volume of 2 mL in 5 cc glass vials (Schott Type 1A) with a total of 4 vials per formulation. All samples were filtered in a sterile hood using Sterivex filter units (0.22 μm) prior to filling. After filing vials were loosely capped with rubber stoppers for lyophilization (FIG. 17A).
Three vials per formulation were lyophilized using a modified conservative lyophilization cycle (−17° C. annealing temperature, 66 hr total cycle time). The remaining one vial per formulation was reserved for t=0 (pre-lyophilization) analysis. Prior to reconstitution, the lyo cakes were visually inspected for structural integrity and elegance. Lyophilized samples were reconstituted with 1.96 mL of Milli-Q water and gently swirled until fully dissolved for further analysis. Pre-lyophilization and post-constitution samples were analyzed by analytical SEC and micro flow imaging (MFI).
SEC results revealed that SBE-β-CD containing formulations generated lower levels of HMW species pre- and post-lyophilization compared to formulations with α-cyclodextran or no cyclodextran at all. Other formulation excipients (sucrose, glycine, mannitol) did not appear to impact levels of HMW species significantly (FIG. 17B, FIG. 17C).
MFI revealed a moderate increase in subvisible particles (majority in the 1-2 μm range) for most formulations following lyophilization. A dramatic increase was observed for one of the α-cyclodextran formulation, C60AcL. Two SBE-β-CD (captisol) containing formulations, C60CpT and C60CpMSuT, contained the least number of subvisible particles after lyophilization (FIG. 17D).

Example 14: Small Scale Formulation Study of Fap Alpha BiTE® Including SBE-β-CD and α-Cyclodextran (UFC, LLPS and F/T)

The purpose of this experiment is to evaluate the stability of Fap alpha BiTE® after various stresses in various formulations. Specifically, FAP alpha BiTE® (SEQ ID NO: 177) was evaluated after LLPS, 20 freeze/thaw (F/T) cycles, and concentration by ultrafiltration/centrifugation (UFC). Results from previous studies with similar formulations have shown that SBE-β-CD have a positive effect on AMG 330 BiTE® stability and in this study, effect on SBE-β-CD on FAP BiTE® was investigated.

Materials and Methods:

30 mL of buffer was prepared for each formulation tested.

TABLE 18

Sample composition and preparation. Control (FRM1) is formulated in 10 mM
Potassium Phosphate, 161 mM Arginine pH 7.6 + 4% Trehalose at 2.65 mg/mL.

	20 mM	1%	1%	40%	10%	15%	55%	18%
Volume in mL	Citrate	PS-80	F-68	SBE-β-CD	α-CD	Glycine	Sucrose	Mannitol

Sample	Sample

ID	composition
FRM1	Control	N/A	N/A	N/A	N/A	N/A	N/A	N/A	N/A
FRM2	Control,	29.7	0.3
	0.01% PS-80
FRM3	0.5% SBE-β-	29.325	0.3		0.375
	CD, 0.01%
	PS-80
FRM4	0.5% SBE-β-	24.78	0.3		0.375		4	0.545
	CD, 2%
	Glycine, 1%
	Sucrose,
	0.01% PS-80
FRM5	0.5% SBE-β-	21.565	0.3		0.375			1.09	6.67
	CD, 4%
	Mannitol, 2%
	Sucrose,
	0.01% PS-80
FRM6	0.5% α-CD,	25.5		3		1.5
	0.1% F-68
FRM7	0.5% α-CD,	20.955		3		1.5	4	0.545
	2% Glycine,
	1% Sucrose,
	0.1% F-68
FRM8	0.5% α-CD,	17.74		3		1.5		1.09	6.67
	4% Mannitol,
	2% Sucrose,
	0.1% F-68

For each sample, 375 μL of 2.65 mg/mL FAP alpha BiTE® (formulated in 10 mM Potassium Phosphate, 161 mM Arginine pH 7.6+4% Trehalose) were placed into an Amicon Ultra 4 mL centrifugal filter tube of MWCO 10,000. 3.5 mL of the appropriate buffer were added to each tube and mixed gently with the protein, and the tubes were centrifuged (Allegra 6R Centrifuge, Beckman Coulter, Brea, Calif., USA) at 4000 rcf at 25 C until retentate volume was-50 uL. The buffer addition and centrifugation steps were repeated twice more for a total of 3 concentration steps. The retentate was then gently mixed with a pipettor, removed from the filter tube, placed in an Eppendorf tube, and microcentrifuged (Eppendorf Centrifuge 5418, St. Louis, Mo., USA) at maximum speed for 2 min. The supernatant was then analyzed by SEC. Each sample was prepared in duplicate. Non-concentrated FAP alpha BiTE® (2.65 mg/mL) was also analyzed for comparison purposes.
The presence of SBE-β-CD appeared to increase relative SEC mainpeak by suppressing the formation of HMW species during protein concentration. The presence of α-cyclodextran resulted in very low protein recovery and high relative levels of HMW species.
Fap alpha LLPS results: LLPS results with Fap a BiTE® and SBE-β-CD are comparable to the LLPS results with AMG 330. α-cyclodextran did not show any positive or negative effect on the colloidal stability of this molecule (FIG. 18 ).

Example 15: Formulation Study for CD33-scFc BiTE Antibody Construct

CD33-scFc BiTE antibody construct was purified using Protein A and cation exchange chromatography (CEX). The CEX eluate was dialyzed into a 10 mM L-glutamic acid buffer at pH 4.2 using dialysis cassettes containing membranes with a molecular weight cut-off (MWCO) of 10 kDa. Dialysis was performed at 2-8° C. The concentration of the dialyzed pool material totaled 2.3 mg/mL. The material was further concentrated via ultrafiltration centrifugation (UFC) using concentrator tubes containing membranes with MWCO of 10 kDa. The concentrated material was filtered with through a filter with a pore size of 0.22 μm. Post filtration concentration totaled 2.7 mg/mL. The material was fully formulated into the formulations listed in Table 19. by spiking with concentrated stock solution. The final protein concentration totals 1.0 mg/mL.

TABLE 19

Overview on tested formulations; HPBCD:
hydroxypropyl-beta-cyclodextrin; PS 80: polysorbate 80.

	L-Glutamic			Trehalose
	acid	Mannitol	Sucrose	dihydrate	HPBCD	PS	80
Designation	[mM\|	[% (w/v)]	[% (w/v)]	[% (w/v)]	[% (w/v)]	[% (w/v)]

G42MSuT	10	4.0	2.0	0.0	0.0	0.01
G42MTrT	10	4.0	0.0	2.0	0.0	0.01
G42SuT	10	0.0	8.0	0.0	0.0	0.01
G42TrT	10	0.0	0.0	8.0	0.0	0.01
G42HP12SuT	10	0.0	4.0	0.0	12.0	0.01
G42HP12TrT	10	0.0	0.0	4.0	12.0	0.01
G42HP6MT	10	4.0	0.0	0.0	6.0	0.01
G42HP6SuT	10	0.0	6.0	0.0	6.0	0.01
G42HP6TrT	10	0.0	0.0	6.0	6.0	0.01

Formulations were filled to 1.0 mL in 2R type I glass vials which were closed with butyl rubber stoppers and aluminum flip off seals. Vials were stored at −20 and −70° C. Samples were pulled at designated time points. After sampling vials were thawed at ambient temperature and analyzed via size exclusion ultra-high performance chromatography (SE-UPLC) in order to quantify the percentaged content of high molecular weight species. SE-UPLC was performed on an Aquity H-Class UPLC system (Waters) using an Acquity UPLC BEH200 SEC 150 mm column (Waters). Column temperature was set to 25° C. Separation of size variants was achieved by applying an isocratic method with a flow rate of 0.4 mL/min. The mobile phase was composed of 100 mM sodium phosphate, 250 mM NaCl pH 6.8. The run time totals 6.0 minutes. Samples were held at 8° C. within the autosampler until analysis. A total amount of 3 μg protein was injected. In order to avoid carry over an intermediate injection with 40% ACN was performed after each sample. Detection was based on fluorescence (excitation at 280 nm, emission at 325 nm). Peak integration was performed using Empower® software. Relative area under the curve of HMWS was reported (FIG. 18 ).
Storage of formulated CD33-scFc BiTE antibody construct at −70° C. or below inhibited the formation of HMWS. However, HMWS significantly increased during storage at −20° C. for formulations that did not contain HPBCD. In contrast, the protein was prevented from forming HMWS at −20° C. in presence of HPBCD irrespective of its concentration (6 or 12%). The presence of mannitol detrimentally affected stability at −20° C. indicated by an increase in HMWS.

Example 16: Formulation Study for FLT3-scFc BiTE Antibody Constructs

Two different FLT3-scFc BiTE antibody constructs (FL1-scFc and FL2-scFc) were purified using protein A and CEX chromatrography. Post CEX all contructs were diafiltered in a buffer composed of 10 mM L-glutamic acid, 4% (w/v) sucrose at pH 4.2. The MWCO of the used membrane was 10 kDa. The diafiltered pool (protein concentration of 1.7 mg/mL) was concentrated via ultrafiltration (MWCO of 10 kDa) until a concentration of 7.6 mg/mL was achieved. The material was then filtered through a 0.2 μm filter and fully formulated through spiking with excipient stock solutions. An overview of formulations is provided by Table 20.

TABLE 20

Overview on tested formulations; pH was adjusted to
4.2 for all formulations; HPBCD:
hydroxypropyl-beta-cyclodextrin; PS 80: polysorbate 80.

		L-Glutamic	Sucrose	HPBCD	PS	80
	Protein	acid	[%	[%	[%
Designation	[mg/mL]	[mM]	(w/v)]	(w/v)]	(w/v)]

G42SuT	5.0	10	9.0	0.0	0.01
G42HP12SuT	5.0	10	4.0	12.0	0.01

Both formulations were filled to 1.3 mL in 2R type I glass vials which were closed with butyl rubber stoppers and aluminum flip off seals. Vials were stored at −20° C. Samples were pulled at designated time points. After sampling vials were thawed at ambient temperature and analyzed via size exclusion ultra-high performance chromatography (SE-UPLC) in order to quantify the percentaged content of high molecular weight species. SE-UPLC was performed on an Aquity H-Class UPLC system (Waters) using an Acquity UPLC BEH200 SEC 150 mm column (Waters). Column temperature was set to 25° C. Separation of size variants was achieved by applying an isocratic method with a flow rate of 0.4 mL/min. The mobile phase was composed of 100 mM sodium phosphate, 250 mM NaCl pH 6.8. The run time totals 6.0 minutes. Samples were held at 8° C. within the autosampler until analysis. A total amount of 3 μg protein was injected. In order to avoid carry over an intermediate injection with 40% ACN was performed after each sample. Detection was based on fluorescence (excitation at 280 nm, emission at 325 nm). Peak integration was performed using Empower® software. Relative area under the curve of HMWS was reported (FIG. 19 ).

Example 17: Formulation Study for BCMA-scFc BiTE Antibody Constructs

Two BCMA-scFc BiTE antibody constructs (BC1-scFc and BC2-scFc) were purified, formulated, stored, and analyzed as described under Example 16. An overview of formulations is provided by Table 21.

TABLE 21

Overview on tested formulations; pH was adjusted to
4.2 for all formulations; HPBCD:
hydroxypropyl-beta-cyclodextrin; PS 80: polysorbate 80.

		L-Glutamic			PS	80
	Protein	acid	Sucrose	HPBCD	[%
Designation	[mg/mL]	[mM]	[% (w/v)]	[% (w/v)]	(w/v)]

G42SuT	5.0	10	9.0	0.0	0.01
G42HP12SuT	5.0	10	6.0	6.0	0.01

FIG. 20 shows the percentaged HMWS content in function of formulation for both antibody constructs. The percentaged content of HMWS increased by 1.6% (BC1-scFc) and 1.9% (BC-scFc) respectively in HPBCD free formulations after four weeks. In contrast HMWS formation was inhibited in formulations containing 6% HPBCD.


SEQ
ID NO:	Description	SEQUENCE

1.	CD3_1	VL CDR1	GSSTGAVTSGYYPN

2.	CD3_1	VL CDR2	GTKFLAP

3.	CD3_1	VL CDR3	ALWYSNRWV

4.	CD3_1	VH CDR1	IYAMN

5.	CD3_1	VH CDR2	RIRSKYNNYATYYADSVKS

6.	CD3_1	VH CDR3	HGNFGNSYVSFFAY

7.	CD3_1	VH	EVQLVESGGGLVQPGGSLKLSCAASGFTFNIYAMNWVRQAPGKGLEWVARIRSKYNNYATYYADSVKSRFTISRDDS
			KNTAYLQMNNLKTEDTAVYYCVRHGNFGNSYVSFFAYWGQGTLVTVSS


8.	CD3_1	VL	QTVVTQEPSLTVSPGGTVTLTCGSSTGAVTSGYYPNWVQQKPGQAPRGLIGGTKFLAPGTPARFSGSLLGGKAALTL
			SGVQPEDEAEYYCALWYSNRWVFGGGTKLTVL


9.	CD3_1	scFv	EVQLVESGGGLVQPGGSLKLSCAASGFTFNIYAMNWVRQAPGKGLEWVARIRSKYNNYATYYADSVKSRFTISRDDS
			KNTAYLQMNNLKTEDTAVYYCVRHGNFGNSYVSFFAYWGQGTLVTVSSGGGGSGGGGSGGGGSQTVVTQEPSLTVSP
			GGTVTLTCGSSTGAVTSGYYPNWVQQKPGQAPRGLIGGTKFLAPGTPARFSGSLLGGKAALTLSGVQPEDEAEYYCA
			LWYSNRWVFGGGTKLTVL


10.	CD3_2	VL CDR1	GSSTGAVTSGYYPN

11.	CD3_2	VL CDR2	GTKFLAP

12.	CD3_2	VL CDR3	ALWYSNRWV

13.	CD3_2	VH CDR1	KYAMN

14.	CD3_2	VH CDR2	RIRSKYNNYATYYADSVKD

15.	CD3_2	VH CDR3	HGNFGNSYISYWAY

16.	CD3_2	VH	EVQLVESGGGLVQPGGSLKLSCAASGFTFNKYAMNWVRQAPGKGLEWVARIRSKYNNYATYYADSVKDRFTISRDDS
			KNTAYLQMNNLKTEDTAVYYCVRHGNFGNSYISYWAYWGQGTLVTVSS


17.	CD3_2	VL	QTVVTQEPSLTVSPGGTVTLTCGSSTGAVTSGYYPNWVQQKPGQAPRGLIGGTKFLAPGTPARFSGSLLGGKAALTL
			SGVQPEDEAEYYCALWYSNRWVFGGGTKLTVL


18.	CD3_2	scFv	EVQLVESGGGLVQPGGSLKLSCAASGFTFNKYAMNWVRQAPGKGLEWVARIRSKYNNYATYYADSVKDRFTISRDDS
			KNTAYLQMNNLKTEDTAVYYCVRHGNFGNSYISYWAYWGQGTLVTVSSGGGGSGGGGSGGGGSQTVVTQEPSLTVSP
			GGTVTLTCGSSTGAVTSGYYPNWVQQKPGQAPRGLIGGTKFLAPGTPARFSGSLLGGKAALTLSGVQPEDEAEYYCA
			LWYSNRWVFGGGTKLTVL


19.	CD3_3	VL CDR1	GSSTGAVTSGYYPN

20.	CD3_3	VL CDR2	GTKFLAP

21.	CD3_3	VL CDR3	ALWYSNRWV

22.	CD3_3	VH CDR1	SYAMN

23.	CD3_3	VH CDR2	RIRSKYNNYATYYADSVKG

24.	CD3_3	VH CDR3	HGNFGNSYLSFWAY

25.	CD3_3	VH	EVQLVESGGGLEQPGGSLKLSCAASGFTFNSYAMNWVRQAPGKGLEWVARIRSKYNNYATYYADSVKGRFTISRDDS
			KNTAYLQMNNLKTEDTAVYYCVRHGNFGNSYLSFWAYWGQGTLVTVSS

26.	CD3_3	VL	QTVVTQEPSLTVSPGGTVTLTCGSSTGAVTSGYYPNWVQQKPGQAPRGLIGGTKFLAPGTPARFSGSLLGGKAALTL
			SGVQPEDEAEYYCALWYSNRWVFGGGTKLTVL

27.	CD3_3	scFv	EVQLVESGGGLEQPGGSLKLSCAASGFTFNSYAMNWVRQAPGKGLEWVARIRSKYNNYATYYADSVKGRFTISRDDS
			KNTAYLQMNNLKTEDTAVYYCVRHGNFGNSYLSFWAYWGQGTLVTVSSGGGGSGGGGSGGGGSQTVVTQEPSLTVSP
			GGTVTLTCGSSTGAVTSGYYPNWVQQKPGQAPRGLIGGTKFLAPGTPARFSGSLLGGKAALTLSGVQPEDEAEYYCA
			LWYSNRWVFGGGTKLTVL

28.	CD3_4	VL CDR1	GSSTGAVTSGYYPN

29.	CD3_4	VL CDR2	GTKFLAP

30.	CD3_4	VL CDR3	ALWYSNRWV

31.	CD3_4	VH CDR1	RYAMN

32.	CD3_4	VH CDR2	RIRSKYNNYATYYADSVKG

33.	CD3_4	VH CDR3	HGNFGNSYLSYFAY

34.	CD3_4	VH	EVQLVESGGGLVQPGGSLKLSCAASGFTFNRYAMNWVRQAPGKGLEWVARIRSKYNNYATYYADSVKGRFTISRDDS
			KNTAYLQMNNLKTEDTAVYYCVRHGNFGNSYLSYFAYWGQGTLVTVSS


35.	CD3_4	VL	QTVVTQEPSLTVSPGGTVTLTCGSSTGAVTSGYYPNWVQQKPGQAPRGLIGGTKFLAPGTPARFSGSLLGGKAALTL
			SGVQPEDEAEYYCALWYSNRWVFGGGTKLTVL

36.	CD3_4	scFv	EVQLVESGGGLVQPGGSLKLSCAASGFTFNRYAMNWVRQAPGKGLEWVARIRSKYNNYATYYADSVKGRFTISRDDS
			KNTAYLQMNNLKTEDTAVYYCVRHGNFGNSYLSYFAYWGQGTLVTVSSGGGGSGGGGSGGGGSQTVVTQEPSLTVSP
			GGTVTLTCGSSTGAVTSGYYPNWVQQKPGQAPRGLIGGTKFLAPGTPARFSGSLLGGKAALTLSGVQPEDEAEYYCA
			LWYSNRWVFGGGTKLTVL

37.	CD3_5	VL CDR1	RSSTGAVTSGYYPN

38.	CD3_5	VL CDR2	ATDMRPS

39.	CD3_5	VL CDR3	ALWYSNRWV

40.	CD3_5	VH CDR1	VYAMN

41.	CD3_5	VH CDR2	RIRSKYNNYATYYADSVKK

42.	CD3_5	VH CDR3	HGNFGNSYLSWWAY

43.	CD3_5	VH	EVQLVESGGGLVQPGGSLKLSCAASGFTFNVYAMNWVRQAPGKGLEWVARIRSKYNNYATYYADSVKKRFTISRDDS
			KNTAYLQMNNLKTEDTAVYYCVRHGNFGNSYLSWWAYWGQGTLVTVSS

44.	CD3_5	VL	QTVVTQEPSLTVSPGGTVTLTCRSSTGAVTSGYYPNWVQQKPGQAPRGLIGATDMRPSGTPARFSGSLLGGKAALTL
			SGVQPEDEAEYYCALWYSNRWVFGGGTKLTVL


45.	CD3_5	scFv	EVQLVESGGGLVQPGGSLKLSCAASGFTFNVYAMNWVRQAPGKGLEWVARIRSKYNNYATYYADSVKKRFTISRDDS
			KNTAYLQMNNLKTEDTAVYYCVRHGNFGNSYLSWWAYWGQGTLVTVSSGGGGSGGGGSGGGGSQTVVTQEPSLTVSP
			GGTVTLTCRSSTGAVTSGYYPNWVQQKPGQAPRGLIGATDMRPSGTPARFSGSLLGGKAALTLSGVQPEDEAEYYCA
			LWYSNRWVFGGGTKLTVL

46.	CD3_6	VL CDR1	GSSTGAVTSGYYPN

47.	CD3_6	VL CDR2

48.	CD3_6	VL CDR3	ALWYSNRWV

49.	CD3_6	VH CDR1	KYAMN

50.	CD3_6	VH CDR2	RIRSKYNNYATYYADSVKS

51.	CD3_6	VH CDR3	HGNFGNSYTSYYAY

52.	CD3_6	VH	EVQLVESGGGLVQPGGSLKLSCAASGFTFNKYAMNWVRQAPGKGLEWVARIRSKYNNYATYYADSVKSRFTISRDDS
			KNTAYLQMNNLKTEDTAVYYCVRHGNFGNSYTSYYAYWGQGTLVTVSS

53.	CD3_6	VL	QTVVTQEPSLTVSPGGTVTLTCGSSTGAVTSGYYPNWVQQKPGQAPRGLIGGTKFLAPGTPARFSGSLLGGKAALTL
			SGVQPEDEAEYYCALWYSNRWVFGGGTKLTVL

54.	CD3_6	scFv	EVQLVESGGGLVQPGGSLKLSCAASGFTFNKYAMNWVRQAPGKGLEWVARIRSKYNNYATYYADSVKSRFTISRDDS
			KNTAYLQMNNLKTEDTAVYYCVRHGNFGNSYTSYYAYWGQGTLVTVSSGGGGSGGGGSGGGGSQTVVTQEPSLTVSP
			GGTVTLTCGSSTGAVTSGYYPNWVQQKPGQAPRGLIGGTKFLAPGTPARFSGSLLGGKAALTLSGVQPEDEAEYYCA
			LWYSNRWVFGGGTKLTVL

55.	CD3_7	VL CDR1	RSSTGAVTSGYYPN

56.	CD3_7	VL CDR2	ATDMRPS

57.	CD3_7	VL CDR3	ALWYSNRWV

58.	CD3_7	VH CDR1	GYAMN

59.	CD3_7	VH CDR2	RIRSKYNNYATYYADSVKE

60.	CD3_7	VH CDR3	HRNFGNSYLSWFAY

61.	CD3_7	VH	EVQLVESGGGLVQPGGSLKLSCAASGFTFNGYAMNWVRQAPGKGLEWVARIRSKYNNYATYYADSVKERFTISRDDS
			KNTAYLQMNNLKTEDTAVYYCVRHRNFGNSYLSWFAYWGQGTLVTVSS

62.	CD3_7	VL	QTVVTQEPSLTVSPGGTVTLTCRSSTGAVTSGYYPNWVQQKPGQAPRGLIGATDMRPSGTPARFSGSLLGGKAALTL
			SGVQPEDEAEYYCALWYSNRWVFGGGTKLTVL

63.	CD3_7	scFv	EVQLVESGGGLVQPGGSLKLSCAASGFTFNGYAMNWVRQAPGKGLEWVARIRSKYNNYATYYADSVKERFTISRDDS
			KNTAYLQMNNLKTEDTAVYYCVRHRNFGNSYLSWFAYWGQGTLVTVSSGGGGSGGGGSGGGGSQTVVTQEPSLTVSP
			GGTVTLTCRSSTGAVTSGYYPNWVQQKPGQAPRGLIGATDMRPSGTPARFSGSLLGGKAALTLSGVQPEDEAEYYCA
			LWYSNRWVFGGGTKLTVL

64.	CD3_8	VL CDR1	GSSTGAVTSGYYPN

65.	CD3_8	VL CDR2	GTKFLAP

66.	CD3_8	VL CDR3	ALWYSNRWV

67.	CD3_8	VH CDR1	VYAMN

68.	CD3_8	VH CDR2	RIRSKYNNYATYYADSVKK

69.	CD3_8	VH CDR3	HGNFGNSYISWWAY

70.	CD3_8	VH	EVQLVESGGGLVQPGGSLKLSCAASGFTFNVYAMNWVRQAPGKGLEWVARIRSKYNNYATYYADSVKKRFTISRDDS
			KNTAYLQMNNLKTEDTAVYYCVRHGNFGNSYISWWAYWGQGTLVTVSS

71.	CD3_8	VL	QTVVTQEPSLTVSPGGTVTLTCGSSTGAVTSGYYPNWVQQKPGQAPRGLIGGTKFLAPGTPARFSGSLLGGKAALTL

		SGVQPEDEAEYYCALWYSNRWVFGGGTKLTVL

72.	CD3_8	scFv	EVQLVESGGGLVQPGGSLKLSCAASGFTFNVYAMNWVRQAPGKGLEWVARIRSKYNNYATYYADSVKKRFTISRDDS
			KNTAYLQMNNLKTEDTAVYYCVRHGNFGNSYISWWAYWGQGTLVTVSSGGGGSGGGGSGGGGSQTVVTQEPSLTVSP
			GGTVTLTCGSSTGAVTSGYYPNWVQQKPGQAPRGLIGGTKFLAPGTPARFSGSLLGGKAALTLSGVQPEDEAEYYCA
			LWYSNRWVFGGGTKLTVL

73.	CD3_9	VL CDR1	GSSTGAVTSGNYPN

74.	CD3_9	VL CDR2	GTKFLAP

75.	CD3_9	VL CDR3	VLWYSNRWV

76.	CD3_9	VH CDR1	SYAMN

77.	CD3_9	VH CDR2	RIRSKYNNYATYYADSVKG

78.	CD3_9	VH CDR3	HGNFGNSYVSWWAY

79.	CD3_9	VH	EVQLVESGGGLVQPGGSLKLSCAASGFTFNSYAMNWVRQAPGKGLEWVARIRSKYNNYATYYADSVKGRFTISRDDS
			KNTAYLQMNNLKTEDTAVYYCVRHGNFGNSYVSWWAYWGQGTLVTVSS


80.	CD3_9	VL	QTVVTQEPSLTVSPGGTVTLTCGSSTGAVTSGNYPNWVQQKPGQAPRGLIGGTKFLAPGTPARFSGSLLGGKAALTL
			SGVQPEDEAEYYCVLWYSNRWVFGGGTKLTVL

81.	CD3_9	scFv	EVQLVESGGGLVQPGGSLKLSCAASGFTFNSYAMNWVRQAPGKGLEWVARIRSKYNNYATYYADSVKGRFTISRDDS
			KNTAYLQMNNLKTEDTAVYYCVRHGNFGNSYVSWWAYWGQGTLVTVSSGGGGSGGGGSGGGGSQTVVTQEPSLTVSP
			GGTVTLTCGSSTGAVTSGNYPNWVQQKPGQAPRGLIGGTKFLAPGTPARFSGSLLGGKAALTLSGVQPEDEAEYYCV
			LWYSNRWVFGGGTKLTVL

82.	CD3_10	VL CDR1	GSSTGAVTSGNYPN

83.	CD3_10	VL CDR2	GTKFLAP

84.	CD3_10	VL CDR3	VLWYSNRWV

85.	CD3_10	VH CDR1	KYAMN

86.	CD3_10	VH CDR2	RIRSKYNNYATYYADSVKD

87.	CD3_10	VH CDR3	HGNFGNSYISYWAY

88.	CD3_10	VH	EVQLVESGGGLVQPGGSLKLSCAASGFTFNKYAMNWVRQAPGKGLEWVARIRSKYNNYATYYADSVKDRFTISRDDS
			KNTAYLQMNNLKTEDTAVYYCVRHGNFGNSYISYWAYWGQGTLVTVSS

89.	CD3_10	VL	QTVVTQEPSLTVSPGGTVTLTCGSSTGAVTSGNYPNWVQQKPGQAPRGLIGGTKFLAPGTPARFSGSLLGGKAALTL
			SGVQPEDEAEYYCVLWYSNRWVFGGGTKLTVL


90.	CD3_10	scFv	EVQLVESGGGLVQPGGSLKLSCAASGFTFNKYAMNWVRQAPGKGLEWVARIRSKYNNYATYYADSVKDRFTISRDDS
			KNTAYLQMNNLKTEDTAVYYCVRHGNFGNSYISYWAYWGQGTLVTVSSGGGGSGGGGSGGGGSQTVVTQEPSLTVSP
			GGTVTLTCGSSTGAVTSGNYPNWVQQKPGQAPRGLIGGTKFLAPGTPARFSGSLLGGKAALTLSGVQPEDEAEYYCV
			LWYSNRWVFGGGTKLTVL

91.	CD33_1	VH CDR1	NYGMN

92.	CD33_1	VH CDR2	WINTYTGEPTYADKFQG

93.	CD33_1	VH CDR3	WSWSDGYYVYFDY

94.	CD33_1	VL CDR1	KSSQSVLDSSTNKNSLA

95.	CD33_1	VL CDR2	WASTRES

96.	CD33_1	VL CDR3	QQSAHFPIT

97.	CD33_1	VH	QVQLVQSGAEVKKPGESVKVSCKASGYTFTNYGMNWVKQAPGQGLEWMGWINTYTGEPTYADKFQGRVTMTTDTSTS
			TAYMEIRNLGGDDTAVYYCARWSWSDGYYVYFDYWGQGTSVTVSS

98.	CD33_1	VL	DIVMTQSPDSLTVSLGERTTINCKSSQSVLDSSTNKNSLAWYQQKPGQPPKLLLSWASTRESGIPDRFSGSGSGTDF
			TLTIDSPQPEDSATYYCQQSAHFPITFGQGTRLEIK

99.	CD33_1	scFv	QVQLVQSGAEVKKPGESVKVSCKASGYTFTNYGMNWVKQAPGQGLEWMGWINTYTGEPTYADKFQGRVTMTTDTSTS
			TAYMEIRNLGGDDTAVYYCARWSWSDGYYVYFDYWGQGTSVTVSSGGGGSGGGGSGGGGSDIVMTQSPDSLTVSLGE
			RTTINCKSSQSVLDSSTNKNSLAWYQQKPGQPPKLLLSWASTRESGIPDRFSGSGSGTDFTLTIDSPQPEDSATYYC
			QQSAHFPITFGQGTRLEIK


100.	CD33_1	bispecific	QVQLVQSGAEVKKPGESVKVSCKASGYTFTNYGMNWVKQAPGQGLEWMGWINTYTGEPTYADKFQGRVTMTTDTSTS
		molecule	TAYMEIRNLGGDDTAVYYCARWSWSDGYYVYFDYWGQGTSVTVSSGGGGSGGGGSGGGGSDIVMTQSPDSLTVSLGE
			RTTINCKSSQSVLDSSTNKNSLAWYQQKPGQPPKLLLSWASTRESGIPDRFSGSGSGTDFTLTIDSPQPEDSATYYC
			QQSAHFPITFGQGTRLEIKSGGGGSEVQLVESGGGLVQPGGSLKLSCAASGFTFNKYAMNWVRQAPGKGLEWVARIR
			SKYNNYATYYADSVKDRFTISRDDSKNTAYLQMNNLKTEDTAVYYCVRHGNFGNSYISYWAYWGQGTLVTVSSGGGG
			SGGGGSGGGGSQTVVTQEPSLTVSPGGTVTLTCGSSTGAVTSGNYPNWVQQKPGQAPRGLIGGTKFLAPGTPARFSG
			SLLGGKAALTLSGVQPEDEAEYYCVLWYSNRWVFGGGTKLTVL

101.	CD33_2	VH CDR1	NYGMN

102.	CD33_2	VH CDR2	WINTYTGEPTYADKFQG

103.	CD33_2	VH CDR3	WSWSDGYYVYFDY

104.	CD33_2	VL CDR1	KSSQSVLDSSTNKNSLA

105.	CD33_2	VL CDR2	WASTRES

106.	CD33_2	VL CDR3	QQSAHFPIT

107.	CD33_2	VH	QVQLVQSGAEVKKPGESVKVSCKASGYTFTNYGMNWVKQAPGQCLEWMGWINTYTGEPTYADKFQGRVTMTTDTSTS
			TAYMEIRNLGGDDTAVYYCARWSWSDGYYVYFDYWGQGTSVTVSS

108.	CD33_2	VL	DIVMTQSPDSLTVSLGERTTINCKSSQSVLDSSTNKNSLAWYQQKPGQPPKLLLSWASTRESGIPDRFSGSGSGTDF
			TLTIDSPQPEDSATYYCQQSAHFPITFGCGTRLEIK

109.	CD33_2	scFv	QVQLVQSGAEVKKPGESVKVSCKASGYTFTNYGMNWVKQAPGQCLEWMGWINTYTGEPTYADKFQGRVTMTTDTSTS
			TAYMEIRNLGGDDTAVYYCARWSWSDGYYVYFDYWGQGTSVTVSSGGGGSGGGGSGGGGSDIVMTQSPDSLTVSLGE
			RTTINCKSSQSVLDSSTNKNSLAWYQQKPGQPPKLLLSWASTRESGIPDRFSGSGSGTDFTLTIDSPQPEDSATYYC
			QQSAHFPITFGCGTRLEIK

110.	CD33_2	bispecific	QVQLVQSGAEVKKPGESVKVSCKASGYTFTNYGMNWVKQAPGQCLEWMGWINTYTGEPTYADKFQGRVTMTTDTSTS
		molecule	TAYMEIRNLGGDDTAVYYCARWSWSDGYYVYFDYWGQGTSVTVSSGGGGSGGGGSGGGGSDIVMTQSPDSLTVSLGE
			RTTINCKSSQSVLDSSTNKNSLAWYQQKPGQPPKLLLSWASTRESGIPDRFSGSGSGTDFTLTIDSPQPEDSATYYC
			QQSAHFPITFGCGTRLEIKSGGGGSEVQLVESGGGLVQPGGSLKLSCAASGFTFNKYAMNWVRQAPGKGLEWVARIR
			SKYNNYATYYADSVKDRFTISRDDSKNTAYLQMNNLKTEDTAVYYCVRHGNFGNSYISYWAYWGQGTLVTVSSGGGG
			SGGGGSGGGGSQTVVTQEPSLTVSPGGTVTLTCGSSTGAVTSGNYPNWVQQKPGQAPRGLIGGTKFLAPGTPARFSG
			SLLGGKAALTLSGVQPEDEAEYYCVLWYSNRWVFGGGTKLTVL

111.	CD33_3	VH CDR1	NYGMN

112.	CD33_3	VH CDR2	WINTYTGEPTYADDFKG

113.	CD33_3	VH CDR3	WSWSDGYYVYFDY

114.	CD33_3	VL CDR1	KSSQSVLDSSKNKNSLA

115.	CD33_3	VL CDR2	WASTRES

116.	CD33_3	VL CDR3	QQSAHFPIT

117.	CD33_3	VH	QVQLVQSGAEVKKPGESVKVSCKASGYTFTNYGMNWVRQAPGQGLEWMGWINTYTGEPTYADDFKGRVTM
			SSDTSTSTAYLEINSLRSDDTAIYYCARWSWSDGYYVYFDYWGQGTTVTVSS

118.	CD33_3	VL	DIVMTQSPDSLTVSLGERTTINCKSSQSVLDSSKNKNSLAWYQQKPGQPPKLLLSWASTRESGIPDRFSG
			SGSGTDFTLTIDSLQPEDSATYYCQQSAHFPITFGQGTRLEIK

119.	CD33_3	scFv	QVQLVQSGAEVKKPGESVKVSCKASGYTFTNYGMNWVRQAPGQGLEWMGWINTYTGEPTYADDFKGRVTM
			SSDTSTSTAYLEINSLRSDDTAIYYCARWSWSDGYYVYFDYWGQGTTVTVSSGGGGSGGGGSGGGGSDIV
			MTQSPDSLTVSLGERTTINCKSSQSVLDSSKNKNSLAWYQQKPGQPPKLLLSWASTRESGIPDRFSGSGS
			GTDFTLTIDSLQPEDSATYYCQQSAHFPITFGQGTRLEIK

120.	CD33_4	VH CDR1	NYGMN

121.	CD33_4	VH CDR2	WINTYTGEPTYADDFKG

122.	CD33_4	VH CDR3	WSWSDGYYVYFDY

123.	CD33_4	VL CDR1	QVQLVQSGAEVKKPGASVKVSCKASGYTFTNYGMNWVKQAPGQGLKWMGWINTYTGEPTYADDFKGRVTM
			TSDTSTSTAYLELHNLRSDDTAVYYCARWSWSDGYYVYFDYWGQGTTVTVSS

124.	CD33_4	VL CDR2	KSSQSVLDSSKNKNSLA

125.	CD33_4	VL CDR3	WASTRES

126.	CD33_4	VH	QQSAHFPIT

127.	CD33_4	VL	DIVMTQSPDSLTVSLGERTTINCKSSQSVLDSSKNKNSLAWYQQKPGQPPKLLLSWASTRESGIPDRFSG
			SGSGTDFTLTIDSLQPEDSATYYCQQSAHFPITFGQGTRLEIK

128.	CD33_4	scFv	QVQLVQSGAEVKKPGASVKVSCKASGYTFTNYGMNWVKQAPGQGLKWMGWINTYTGEPTYADDFKGRVTM
			TSDTSTSTAYLELHNLRSDDTAVYYCARWSWSDGYYVYFDYWGQGTTVTVSSGGGGSGGGGSGGGGSDIV
			MTQSPDSLTVSLGERTTINCKSSQSVLDSSKNKNSLAWYQQKPGQPPKLLLSWASTRESGIPDRFSGSGS
			GTDFTLTIDSLQPEDSATYYCQQSAHFPITFGQGTRLEIK

129.	CD33_5	VH CDR1	NYGMN

130.	CD33_5	VH CDR2	WINTYTGEPTYADDFKG

131.	CD33_5	VH CDR3	WSWSDGYYVYFDY

132.	CD33_5	VL CDR1	KSSQSVLDSSKNKNSLA

133.	CD33_5	VL CDR2	WASTRES

134.	CD33_5	VL CDR3	QQSAHFPIT

135.	CD33_5	VH	QVQLVQSGAEVKKPGESVKVSCKASGYTFTNYGMNWVKQAPGQGLKWMGWINTYTGEPTYADDFKGRVTM
			TTDTSTSTAYMEIRNLRNDDTAVYYCARWSWSDGYYVYFDYWGQGTTVTVSS

136.	CD33_5	VL	DIVMTQSPDSLTVSLGERTTINCKSSQSVLDSSKNKNSLAWYQQKPGQPPKLLLSWASTRESGIPDRFSG
			SGSGTDFTLTIDSLQPEDSATYYCQQSAHFPITFGQGTRLEIK

137.	CD33_5	scFv	QVQLVQSGAEVKKPGESVKVSCKASGYTFTNYGMNWVKQAPGQGLKWMGWINTYTGEPTYADDFKGRVTM
			TTDTSTSTAYMEIRNLRNDDTAVYYCARWSWSDGYYVYFDYWGQGTTVTVSSGGGGSGGGGSGGGGSDIV
			MTQSPDSLTVSLGERTTINCKSSQSVLDSSKNKNSLAWYQQKPGQPPKLLLSWASTRESGIPDRFSGSGS
			GTDFTLTIDSLQPEDSATYYCQQSAHFPITFGQGTRLEIK

138.	CD33_6	VH CDR1	NYGMN

139.	CD33_6	VH CDR2	WINTYTGEPTYADDFKG

140.	CD33_6	VH CDR3	WSWSDGYYVYFDY

141.	CD33_6	VL CDR1	KSSQSVLDSSKNKNSLA

142.	CD33_6	VL CDR2	WASTRES

143.	CD33_6	VL CDR3	QQSAHFPIT

144.	CD33_6	VH	QVQLVQSGAEVKKPGESVKVSCKASGYTFTNYGMNWVKQAPGQGLKWMGWINTYTGEPTYADDFKGRVTM
			TSDTSTSTAYMEISSLRSDDTAVYYCARWSWSDGYYVYFDYWGQGTTVTVSS

145.	CD33_6	VL	DIVMTQSPDSLTVSLGERTTINCKSSQSVLDSSKNKNSLAWYQQKPGQPPKLLLSWASTRESGIPDRFSG
			SGSGTDFTLTIDSLQPEDSATYYCQQSAHFPITFGQGTRLEIK

146.	CD33_6	scFv	QVQLVQSGAEVKKPGESVKVSCKASGYTFTNYGMNWVKQAPGQGLKWMGWINTYTGEPTYADDFKGRVTM
			TSDTSTSTAYMEISSLRSDDTAVYYCARWSWSDGYYVYFDYWGQGTTVTVSSGGGGSGGGGSGGGGSDIV
			MTQSPDSLTVSLGERTTINCKSSQSVLDSSKNKNSLAWYQQKPGQPPKLLLSWASTRESGIPDRFSGSGS
			GTDFTLTIDSLQPEDSATYYCQQSAHFPITFGQGTRLEIK

147.	CD33_7	VH CDR1	NYGMN

148.	CD33_7	VH CDR2	WINTYTGETNYADKFQG

149.	CD33_7	VH CDR3	WSWSDGYYVYFDY

150.	CD33_7	VL CDR1	KSSQSVLDSSTNKNSLA

151.	CD33_7	VL CDR2	WASTRE

152.	CD33_7	VL CDR3	QQSAHFPIT

153.	CD33_7	VH	QVQLVQSGAEVKKPGESVKVSCKASGYTFTNYGMNWVKQAPGQGLEWMGWINTYTGETNYADKFQGRVTF
			TSDTSTSTAYMELRNLKSDDTAVYYCARWSWSDGYYVYFDYWGQGTTVTVSS

154.	CD33_7	VL	DIVMTQSPDSMTVSLGERTTINCKSSQSVLDSSTNKNSLAWYQQKPGQPPKLLLSWASTRESGIPDRFSG
			SGSGTDFTLTIDSLQPEDSATYYCQQSAHFPITFGQGTRLDIK

155.	CD33_7	scFv	QVQLVQSGAEVKKPGESVKVSCKASGYTFTNYGMNWVKQAPGQGLEWMGWINTYTGETNYADKFQGRVTF
			TSDTSTSTAYMELRNLKSDDTAVYYCARWSWSDGYYVYFDYWGQGTTVTVSSGGGGSGGGGSGGGGSDIV
			MTQSPDSMTVSLGERTTINCKSSQSVLDSSTNKNSLAWYQQKPGQPPKLLLSWASTRESGIPDRFSGSGS
			GTDFTLTIDSLQPEDSATYYCQQSAHFPITFGQGTRLDIK

156.	CD33_8	VH CDR1	NYGMN

157.	CD33_8	VH CDR2	WINTYTGETNYADKFQG

158.	CD33_8	VH CDR3	WSWSDGYYVYFDY

159.	CD33_8	VL CDR1	KSSQSVLDSSTNKNSLA

160.	CD33_8	VL CDR2	WASTRES

161.	CD33_8	VL CDR3	QQSAHFPIT

162.	CD33_8	VH	QVQLVQSGAEVKKPGESVKVSCKASGYTFTNYGMNWVKQAPGQGLEWMGWINTYTGETNYADKFQGRVTF
			TSDTSTSTAYMELRNLKSDDTAVYYCARWSWSDGYYVYFDYWGQGTTVTVSS

163.	CD33_8	VL	DIVMTQSPDSLSVSLGERTTINCKSSQSVLDSSTNKNSLAWYQQKPGQPPKLLLSWASTRESGIPDRFSG
			SGSGTDFTLTIDSLQPEDSATYYCQQSAHFPITFGQGTRLEIK

164.	CD33_8	scFv	QVQLVQSGAEVKKPGESVKVSCKASGYTFTNYGMNWVKQAPGQGLEWMGWINTYTGETNYADKFQGRVTF
			TSDTSTSTAYMELRNLKSDDTAVYYCARWSWSDGYYVYFDYWGQGTTVTVSSGGGGSGGGGSGGGGSDIV
			MTQSPDSLSVSLGERTTINCKSSQSVLDSSTNKNSLAWYQQKPGQPPKLLLSWASTRESGIPDRFSGSGS
			GTDFTLTIDSLQPEDSATYYCQQSAHFPITFGQGTRLEIK

165.	CD33_9	VH CDR1	NYGMN

166.	CD33_9	VH CDR2	WINTYTGEPTYADKFQG

167.	CD33_9	VH CDR3	WSWSDGYYVYFDY

168.	CD33_9	VL CDR1	KSSQSVLDSSNNKNSLA

169.	CD33_9	VL CDR2	WASTRES

170.	CD33_9	VL CDR3	QQSAHFPIT

171.	CD33_9	VH	QVQLVQSGAEVKKPGESVKVSCKASGYTFTNYGMNWVKQAPGQGLEWMGWINTYTGEPTYADKFQGRVTM
			TTDTSTSTAYMEIRNLRSDDTAVYYCARWSWSDGYYVYFDYWGQGTTVTVSS

172.	CD33_9	VL	DIVMTQSPDSLTVSLGERTTINCKSSQSVLDSSNNKNSLAWYQQKPGQPPKLLLSWASTRESGIPDRFSG
			SGSGTDFTLTIDGLQPEDSATYYCQQSAHFPITFGQGTRLEIK

173.	CD33_9	scFv	QVQLVQSGAEVKKPGESVKVSCKASGYTFTNYGMNWVKQAPGQGLEWMGWINTYTGEPTYADKFQGRVTM
			TTDTSTSTAYMEIRNLRSDDTAVYYCARWSWSDGYYVYFDYWGQGTTVTVSSGGGGSGGGGSGGGGSDIV
			MTQSPDSLTVSLGERTTINCKSSQSVLDSSNNKNSLAWYQQKPGQPPKLLLSWASTRESGIPDRFSGSGS
			GTDFTLTIDGLQPEDSATYYCQQSAHFPITFGQGTRLEIK

174.	CD19	bispecific	DIQLTQSPASLAVSLGQRATISCKASQSVDYDGDSYLNWYQQIPGQPPKLLIYDASNLVSGIPPRFSGSGSGTDFTL
		molecule	NIHPVEKVDAATYHCQQSTEDPWTFGGGTKLEIKGGGGSGGGGSGGGGSQVQLQQSGAELVRPGSSVKISCKASGYA
			FSSYWMNWVKQRPGQGLEWIGQIWPGDGDTNYNGKFKGKATLTADESSSTAYMQLSSLASEDSAVYFCARRETTTVG
			RYYYAMDYWGQGTTVTVSSGGGGSDIKLQQSGAELARPGASVKMSCKTSGYTFTRYTMHWVKQRPGQGLEWIGYINP
			SRGYTNYNQKFKDKATLTTDKSSSTAYMQLSSLTSEDSAVYYCARYYDDHYCLDYWGQGTTLTVSSVEGGSGGSGGS
			GGSGGVDDIQLTQSPAIMSASPGEKVTMTCRASSSVSYMNWYQQKSGTSPKRWIYDTSKVASGVPYRFSGSGSGTSY
			SLTISSMEAEDAATYYCQQWSSNPLTFGAGTKLELKHHHHHH

175.	CD33_2	bispecific	QVQLVQSGAEVKKPGESVKVSCKASGYTFTNYGMNWVKQAPGQCLEWMGWINTYTGEPTYADKFQGRVTMTTDTSTS
		molecule +	TAYMEIRNLGGDDTAVYYCARWSWSDGYYVYFDYWGQGTSVTVSSGGGGSGGGGSGGGGSDIVMTQSPDSLTVSLGE
		hALB	RTTINCKSSQSVLDSSTNKNSLAWYQQKPGQPPKLLLSWASTRESGIPDRFSGSGSGTDFTLTIDSPQPEDSATYYC
			QQSAHFPITFGCGTRLEIKSGGGGSEVQLVESGGGLVQPGGSLKLSCAASGFTFNKYAMNWVRQAPGKGLEWVARIR
			SKYNNYATYYADSVKDRFTISRDDSKNTAYLQMNNLKTEDTAVYYCVRHGNFGNSYISYWAYWGQGTLVTVSSGGGG
			SGGGGSGGGGSQTVVTQEPSLTVSPGGTVTLTCGSSTGAVTSGNYPNWVQQKPGQAPRGLIGGTKFLAPGTPARFSG
			SLLGGKAALTLSGVQPEDEAEYYCVLWYSNRWVFGGGTKLTVLPGGGGSDAHKSEVAHRFKDLGEENFKALVLIAFA
			QYLQQCPFEDHVKLVNEVTEFAKTCVADESAENCDKSLHTLFGDKLCTVATLRETYGEMADCCAKQEPERNECFLQH
			KDDNPNLPRLVRPEVDVMCTAFHDNEETFLKKYLYEIARRHPYFYAPELLFFAKRYKAAFTECCQAADKAACLLPKL
			DELRDEGKASSAKQRLKCASLQKFGERAFKAWAVARLSQRFPKAEFAEVSKLVTDLTKVHTECCHGDLLECADDRAD
			LAKYICENQDSISSKLKECCEKPLLEKSHCIAEVENDEMPADLPSLAADFVESKDVCKNYAEAKDVFLGMFLYEYAR
			RHPDYSVVLLLRLAKTYETTLEKCCAAADPHECYAKVFDEFKPLVEEPQNLIKQNCELFEQLGEYKFQNALLVRYTK
			KVPQVSTPTLVEVSRNLGKVGSKCCKHPEAKRMPCAEDYLSVVLNQLCVLHEKTPVSDRVTKCCTESLVNRRPCFSA
			LEVDETYVPKEFNAETFTFHADICTLSEKERQIKKQTALVELVKHKPKATKEQLKAVMDDFAAFVEKCCKADDKETC
			FAEEGKKLVAASQAALGLDYHHHHHH

176.	MS_4	bispecific	QVQLVESGGGLVKPGGSLRLSCAASGFTFSDYYMTWIRQAPGKGLEWLSYISSSGSTIYYADSVKGRFTISRDNAKN
		molecule +	SLFLQMNSLRAEDTAVYYCARDRNSHFDYWGQGTLVTVSSGGGGSGGGGSGGGGSDIQMTQSPSSVSASVGDRVTIT
		hALB	CRASQGINTWLAWYQQKPGKAPKLLIYGASGLQSGVPSRFSGSGSGTDFTLTISSLQPEDFATYYCQQAKSFPRTFG
			QGTKVEIKSGGGGSEVQLVESGGGLVQPGGSLKLSCAASGFTFNKYAMNWVRQAPGKGLEWVARIRSKYNNYATYYA
			DSVKDRFTISRDDSKNTAYLQMNNLKTEDTAVYYCVRHGNFGNSYISYWAYWGQGTLVTVSSGGGGSGGGGSGGGGS
			QTVVTQEPSLTVSPGGTVTLTCGSSTGAVTSGNYPNWVQQKPGQAPRGLIGGTKFLAPGTPARFSGSLLGGKAALTL
			SGVQPEDEAEYYCVLWYSNRWVFGGGTKLTVLPGGGGSDAHKSEVAHRFKDLGEENFKALVLIAFAQYLQQCPFEDH
			VKLVNEVTEFAKTCVADESAENCDKSLHTLFGDKLCTVATLRETYGEMADCCAKQEPERNECFLQHKDDNPNLPRLV
			RPEVDVMCTAFHDNEETFLKKYLYEIARRHPYFYAPELLFFAKRYKAAFTECCQAADKAACLLPKLDELRDEGKASS
			AKQRLKCASLQKFGERAFKAWAVARLSQRFPKAEFAEVSKLVTDLTKVHTECCHGDLLECADDRADLAKYICENQDS
			ISSKLKECCEKPLLEKSHCIAEVENDEMPADLPSLAADFVESKDVCKNYAEAKDVFLGMFLYEYARRHPDYSVVLLL
			RLAKTYETTLEKCCAAADPHECYAKVFDEFKPLVEEPQNLIKQNCELFEQLGEYKFQNALLVRYTKKVPQVSTPTLV
			EVSRNLGKVGSKCCKHPEAKRMPCAEDYLSVVLNQLCVLHEKTPVSDRVTKCCTESLVNRRPCFSALEVDETYVPKE
			FNAETFTFHADICTLSEKERQIKKQTALVELVKHKPKATKEQLKAVMDDFAAFVEKCCKADDKETCFAEEGKKLVAA
			SQAALGLDYHHHHHH

177.	FAPa	bispecific	QVQLVQSGAEVKKPGASVKVSCKASGYTFTEYTIHWVRQAHGQSLEWMGGINPNNGIPNYNQKFKGRVTI
		molecule	TVDTSASTAYMELRSLRSEDTAVYYCARRRIAYGYDEGHAMDYWGQGTLVTVSSGGGGSGGGGSGGGGSD
			IVMTQTPFSLPVTPGEPASISCKSSQSLLYSRNQKNYLAWYQQKPGQSPKLLIYWASTRESGVPDRFSGS
			GSGTDFTLKISRVEAEDVGVYYCQQYFSYPLTFGGGTKVEIKSGGGGSEVQLVESGGGLVQPGGSLKLSC
			AASGFTFNKYAMNWVRQAPGKGLEWVARIRSKYNNYATYYADSVKDRFTISRDDSKNTAYLQMNNLKTED
			TAVYYCVRHGNFGNSYISYWAYWGQGTLVTVSSGGGGSGGGGSGGGGSQTVVTQEPSLTVSPGGTVTLTC
			GSSTGAVTSGNYPNWVQQKPGQAPRGLIGGTKFLAPGTPARFSGSLLGGKAALTLSGVQPEDEAEYYCVL
			WYSNRWVFGGGTKLTVLHHHHHH

178.	G4S	linker	GGGS

179.	F12q	scFv	EVQLVESGGGLVQPGGSLRLSCAASGFTFNSYAMNWVRQAPGKGLEWVARIRSKYNNYATYYADSVKGRFTISRDDS
			KNTAYLQMNSLKTEDTAVYYCVRHGNFGNSYVSWWAYWGQGTLVTVSSGGGGSGGGGSGGGGSQTVVTQEPSLTVSP
			GGTVTLTCGSSTGAVTSGNYPNWVQQKPGQAPRGLIGGTKFLAPGTPARFSGSLLGGKAALTLSGVQPEDEAEYYCV
			LWYSNRWVFGGGTKLTVL

180.	CD33-scFc BiTE	bispecific	QVQLVQSGAEVKKPGESVKVSCKASGYTFTNYGMNWVKQAPGQCLEWMGWINTYTGEPTYADKFQGRVTMTTDTSTS
	antibody construct	HLE molecule	TAYMEIRNLGGDDTAVYYCARWSWSDGYYVYFDYWGQGTSVTVSSGGGGSGGGGSGGGGSDIVMTQSPDSLTVSLGE
	CD33_2-scFc		RTTINCKSSQSVLDSSTNKNSLAWYQQKPGQPPKLLLSWASTRESGIPDRFSGSGSGTDFTLTIDSPQPEDSATYYC
			QQSAHFPITFGCGTRLEIKSGGGGSEVQLVESGGGLVQPGGSLKLSCAASGFTFNKYAMNWVRQAPGKGLEWVARIR
			SKYNNYATYYADSVKDRFTISRDDSKNTAYLQMNNLKTEDTAVYYCVRHGNFGNSYISYWAYWGQGTLVTVSSGGGG
			SGGGGSGGGGSQTVVTQEPSLTVSPGGTVTLTCGSSTGAVTSGNYPNWVQQKPGQAPRGLIGGTKFLAPGTPARFSG
			SLLGGKAALTLSGVQPEDEAEYYCVLWYSNRWVFGGGTKLTVLGGGGDKTHTCPPCPAPELLGGPSVFLFPPKPKDT
			LMISRTPEVTCVVVDVSHEDPEVKFNWYVDGVEVHNAKTKPCEEQYGSTYRCVSVLTVLHQDWLNGKEYKCKVSNKA
			LPAPIEKTISKAKGQPREPQVYTLPPSREEMTKNQVSLTCLVKGFYPSDIAVEWESNGQPENNYKTTPPVLDSDGSF
			FLYSKLTVDKSRWQQGNVFSCSVMHEALHNHYTQKSLSLSPGKGGGGSGGGGSGGGGSGGGGSGGGGSGGGGSDKTH
			TCPPCPAPELLGGPSVFLFPPKPKDTLMISRTPEVTCVVVDVSHEDPEVKFNWYVDGVEVHNAKTKPCEEQYGSTYR
			CVSVLTVLHQDWLNGKEYKCKVSNKALPAPIEKTISKAKGQPREPQVYTLPPSREEMTKNQVSLTCLVKGFYPSDIA
			VEWESNGQPENNYKTTPPVLDSDGSFFLYSKLTVDKSRWQQGNVFSCSVMHEALHNHYTQKSLSLSPGK

181.	FL1	scFv	QVTLKESGPTLVKPTETLTLTCTLSGFSLNNARMGVSWIRQPPGKCLEWLAHIFSNDEKSYSTSLKNRLTISKDSSK
			TQVVLTMTNVDPVDTATYYCARIVGYGSGWYGFFDYWGQGTLVTVSSGGGGSGGGGSGGGGSDIQMTQSPSSLSASV
			GDRVTITCRASQGIRNDLGWYQQKPGKAPKRLIYAASTLQSGVPSRFSGSGSGTEFTLTISSLQPEDFATYYCLQHN
			SYPLTFGCGTKVEIK

182.	FLT3-scFc BiTE	bispecific	QVTLKESGPTLVKPTETLTLTCTLSGFSLNNARMGVSWIRQPPGKCLEWLAHIFSNDEKSYSTSLKNRLTISKDSSK
	antibody construct	HLE molecule	TQVVLTMTNVDPVDTATYYCARIVGYGSGWYGFFDYWGQGTLVTVSSGGGGSGGGGSGGGGSDIQMTQSPSSLSASV
	FL1-scFc		GDRVTITCRASQGIRNDLGWYQQKPGKAPKRLIYAASTLQSGVPSRFSGSGSGTEFTLTISSLQPEDFATYYCLQHN
			SYPLTFGCGTKVEIKSGGGGSEVQLVESGGGLVQPGGSLKLSCAASGFTFNKYAMNWVRQAPGKGLEWVARIRSKYN
			NYATYYADSVKDRFTISRDDSKNTAYLQMNNLKTEDTAVYYCVRHGNFGNSYISYWAYWGQGTLVTVSSGGGGSGGG
			GSGGGGSQTVVTQEPSLTVSPGGTVTLTCGSSTGAVTSGNYPNWVQQKPGQAPRGLIGGTKFLAPGTPARFSGSLLG
			GKAALTLSGVQPEDEAEYYCVLWYSNRWVFGGGTKLTVLGGGGDKTHTCPPCPAPELLGGPSVFLFPPKPKDTLMIS
			RTPEVTCVVVDVSHEDPEVKFNWYVDGVEVHNAKTKPCEEQYGSTYRCVSVLTVLHQDWLNGKEYKCKVSNKALPAP
			IEKTISKAKGQPREPQVYTLPPSREEMTKNQVSLTCLVKGFYPSDIAVEWESNGQPENNYKTTPPVLDSDGSFFLYS
			KLTVDKSRWQQGNVFSCSVMHEALHNHYTQKSLSLSPGKGGGGSGGGGSGGGGSGGGGSGGGGSGGGGSDKTHTCPP
			CPAPELLGGPSVFLFPPKPKDTLMISRTPEVTCVVVDVSHEDPEVKFNWYVDGVEVHNAKTKPCEEQYGSTYRCVSV
			LTVLHQDWLNGKEYKCKVSNKALPAPIEKTISKAKGQPREPQVYTLPPSREEMTKNQVSLTCLVKGFYPSDIAVEWE
			SNGQPENNYKTTPPVLDSDGSFFLYSKLTVDKSRWQQGNVFSCSVMHEALHNHYTQKSLSLSPGK

183.	FL2	scFv	QVTLKESGPALVKPTETLTLTCTLSGFSLNNARMAVSWIRQPPGKCLEWLAHIFSNDEKSYSTSLKSRLTISKDTSK
			SQVVLTMTNMDPEDTATYYCARIVGYGTGWYGFFDYWGQGILVTVSSGGGGSGGGGSGGGGSDIQMTQSPSSLSASV
			GDRVTITCRASQGIRNDLAWYQQKPGKAPKRLIYAASSLQSGVPSRFSGSGSGTEFTLTISSLQPEDFATYYCLQHN
			SYPLTFGCGTKVEIK

184.	FLT3-scFc BiTE	bispecific	QVTLKESGPALVKPTETLTLTCTLSGFSLNNARMAVSWIRQPPGKCLEWLAHIFSNDEKSYSTSLKSRLTISKDTSK
	antibody construct	HLE molecule	SQVVLTMTNMDPEDTATYYCARIVGYGTGWYGFFDYWGQGILVTVSSGGGGSGGGGSGGGGSDIQMTQSPSSLSASV
	FL2-scFc		GDRVTITCRASQGIRNDLAWYQQKPGKAPKRLIYAASSLQSGVPSRFSGSGSGTEFTLTISSLQPEDFATYYCLQHN
			SYPLTFGCGTKVEIKSGGGGSEVQLVESGGGLVQPGGSLKLSCAASGFTFNKYAMNWVRQAPGKGLEWVARIRSKYN
			NYATYYADSVKDRFTISRDDSKNTAYLQMNNLKTEDTAVYYCVRHGNFGNSYISYWAYWGQGTLVTVSSGGGGSGGG
			GSGGGGSQTVVTQEPSLTVSPGGTVTLTCGSSTGAVTSGNYPNWVQQKPGQAPRGLIGGTKFLAPGTPARFSGSLLG
			GKAALTLSGVQPEDEAEYYCVLWYSNRWVFGGGTKLTVLGGGGDKTHTCPPCPAPELLGGPSVFLFPPKPKDTLMIS
			RTPEVTCVVVDVSHEDPEVKFNWYVDGVEVHNAKTKPCEEQYGSTYRCVSVLTVLHQDWLNGKEYKCKVSNKALPAP
			IEKTISKAKGQPREPQVYTLPPSREEMTKNQVSLTCLVKGFYPSDIAVEWESNGQPENNYKTTPPVLDSDGSFFLYS
			KLTVDKSRWQQGNVFSCSVMHEALHNHYTQKSLSLSPGKGGGGSGGGGSGGGGSGGGGSGGGGSGGGGSDKTHTCPP
			CPAPELLGGPSVFLFPPKPKDTLMISRTPEVTCVVVDVSHEDPEVKFNWYVDGVEVHNAKTKPCEEQYGSTYRCVSV
			LTVLHQDWLNGKEYKCKVSNKALPAPIEKTISKAKGQPREPQVYTLPPSREEMTKNQVSLTCLVKGFYPSDIAVEWE
			SNGQPENNYKTTPPVLDSDGSFFLYSKLTVDKSRWQQGNVFSCSVMHEALHNHYTQKSLSLSPGK

185.	BC1	scFv	QVQLVQSGAEVKKPGASVKVSCKASGYTFTNHIIHWVRQAPGQCLEWMGYINPYPGYHAYNEKFQGRATMTSDTSTS
			TVYMELSSLRSEDTAVYYCARDGYYRDTDVLDYWGQGTLVTVSSGGGGSGGGGSGGGGSDIQMTQSPSSLSASVGDR
			VTITCQASQDISNYLNWYQQKPGKAPKLLIYYTSRLHTGVPSRFSGSGSGTDFTFTISSLEPEDIATYYCQQGNTLP
			WTFGCGTKLEIK


186.	BCMA-scFc BiTE 1	bispecific	QVQLVQSGAEVKKPGASVKVSCKASGYTFTNHIIHWVRQAPGQCLEWMGYINPYPGYHAYNEKFQGRATMTSDTSTS
	antibody construct	HLE molecule	TVYMELSSLRSEDTAVYYCARDGYYRDTDVLDYWGQGTLVTVSSGGGGSGGGGSGGGGSDIQMTQSPSSLSASVGDR
	BC1-scFc		VTITCQASQDISNYLNWYQQKPGKAPKLLIYYTSRLHTGVPSRFSGSGSGTDFTFTISSLEPEDIATYYCQQGNTLP
			WTFGCGTKLEIKSGGGGSEVQLVESGGGLVQPGGSLKLSCAASGFTFNKYAMNWVRQAPGKGLEWVARIRSKYNNYA
			TYYADSVKDRFTISRDDSKNTAYLQMNNLKTEDTAVYYCVRHGNFGNSYISYWAYWGQGTLVTVSSGGGGSGGGGSG
			GGGSQTVVTQEPSLTVSPGGTVTLTCGSSTGAVTSGNYPNWVQQKPGQAPRGLIGGTKFLAPGTPARFSGSLLGGKA
			ALTLSGVQPEDEAEYYCVLWYSNRWVFGGGTKLTVLGGGGDKTHTCPPCPAPELLGGPSVFLFPPKPKDTLMISRTP
			EVTCVVVDVSHEDPEVKFNWYVDGVEVHNAKTKPCEEQYGSTYRCVSVLTVLHQDWLNGKEYKCKVSNKALPAPIEK
			TISKAKGQPREPQVYTLPPSREEMTKNQVSLTCLVKGFYPSDIAVEWESNGQPENNYKTTPPVLDSDGSFFLYSKLT
			VDKSRWQQGNVFSCSVMHEALHNHYTQKSLSLSPGKGGGGSGGGGSGGGGSGGGGSGGGGSGGGGSDKTHTCPPCPA
			PELLGGPSVFLFPPKPKDTLMISRTPEVTCVVVDVSHEDPEVKFNWYVDGVEVHNAKTKPCEEQYGSTYRCVSVLTV
			LHQDWLNGKEYKCKVSNKALPAPIEKTISKAKGQPREPQVYTLPPSREEMTKNQVSLTCLVKGFYPSDIAVEWESNG
			QPENNYKTTPPVLDSDGSFFLYSKLTVDKSRWQQGNVFSCSVMHEALHNHYTQKSLSLSPGK

187.	BC2	scFv	QVQLVQSGAEVKKPGASVKVSCKASGYTFTNHIIHWVRQAPGQGLEWMGYINPYPGYHAYNEKFQGRATMTSDTSTS
			TVYMELSSLRSEDTAVYYCARDGYYRDTDVLDYWGQGTLVTVSSGGGGSGGGGSGGGGSDIQMTQSPSSLSASVGDR
			VTITCQASQDISNYLNWYQQKPGKAPKLLIYYTSRLHTGVPSRFSGSGSGTDFTFTISSLEPEDIATYYCQQGNTLP
			WTFGQGTKLEIK

188.	BCMA-scFc BiTE 2	bispecific	QVQLVQSGAEVKKPGASVKVSCKASGYTFTNHIIHWVRQAPGQGLEWMGYINPYPGYHAYNEKFQGRATMTSDTSTS
	antibody construct	HLE molecule	TVYMELSSLRSEDTAVYYCARDGYYRDTDVLDYWGQGTLVTVSSGGGGSGGGGSGGGGSDIQMTQSPSSLSASVGDR
	BC2-scFc		VTITCQASQDISNYLNWYQQKPGKAPKLLIYYTSRLHTGVPSRFSGSGSGTDFTFTISSLEPEDIATYYCQQGNTLP
			WTFGQGTKLEIKSGGGGSEVQLVESGGGLVQPGGSLKLSCAASGFTFNKYAMNWVRQAPGKGLEWVARIRSKYNNYA
			TYYADSVKDRFTISRDDSKNTAYLQMNNLKTEDTAVYYCVRHGNFGNSYISYWAYWGQGTLVTVSSGGGGSGGGGSG
			GGGSQTVVTQEPSLTVSPGGTVTLTCGSSTGAVTSGNYPNWVQQKPGQAPRGLIGGTKFLAPGTPARFSGSLLGGKA
			ALTLSGVQPEDEAEYYCVLWYSNRWVFGGGTKLTVLGGGGDKTHTCPPCPAPELLGGPSVFLFPPKPKDTLMISRTP
			EVTCVVVDVSHEDPEVKFNWYVDGVEVHNAKTKPCEEQYGSTYRCVSVLTVLHQDWLNGKEYKCKVSNKALPAPIEK
			TISKAKGQPREPQVYTLPPSREEMTKNQVSLTCLVKGFYPSDIAVEWESNGQPENNYKTTPPVLDSDGSFFLYSKLT
			VDKSRWQQGNVFSCSVMHEALHNHYTQKSLSLSPGKGGGGSGGGGSGGGGSGGGGSGGGGSGGGGSDKTHTCPPCPA
			PELLGGPSVFLFPPKPKDTLMISRTPEVTCVVVDVSHEDPEVKFNWYVDGVEVHNAKTKPCEEQYGSTYRCVSVLTV
			LHQDWLNGKEYKCKVSNKALPAPIEKTISKAKGQPREPQVYTLPPSREEMTKNQVSLTCLVKGFYPSDIAVEWESNG
			QPENNYKTTPPVLDSDGSFFLYSKLTVDKSRWQQGNVFSCSVMHEALHNHYTQKSLSLSPGK

Claims

1. A pharmaceutical composition comprising a bispecific single chain antibody construct that binds to target cell surface antigen CD19 via a first binding domain and to the T cell surface antigen CD3 via a second binding domain, a β-cyclodextrin and a buffer,

wherein the binding domains have pairs of VH regions and VL regions in the format of a single chain antibody (scFv),

wherein the composition is characterized by a reduction or prevention of the formation of protein aqqregates (high molecular weight species (HMWS)), and

wherein the β-cyclodextrin is not hydroxypropyl-β-cyclodextrin.

2. The composition according to claim 1, wherein the β-cyclodextrin is selected from the group consisting of β-cyclodextrin, methyl-β-cyclodextrin, hydroxyethyl-β-cyclodextrin, ethyl-β-cyclodextrin, butyl-β-cyclodextrin Succinyl-(2-hydroxypropyl)-β-cyclodextrin, heptakis(2,3,6-tri-O-methyl)-β-cyclodextrin, heptakis(2,3,6-tri-O-benzoyl)-β-cyclodextrin, β-cyclodextrin phosphate sodium salt, β-cyclodextrin sulphate sodium salt, triacetyl-β-cyclodextrin, heptakis(6-O-sulfo)-β-cyclodextrin heptasodium salt, carboxymethyl-β-cyclodextrin sodium salt, sulfobutylether-β-cyclodextrin sodium salt, and 6-O-p-toluenesulfonyl-β-cyclodextrin.

3. The composition according to claim 1, wherein the β-cyclodextrin is present in a concentration in the range of 0.1% to 20% (w/v).

4. The composition according to claim 1, wherein the β-cyclodextrin is sulfobutylether-β-cyclodextrin sodium salt.

5. The composition according to claim 1, wherein the bispecific single chain antibody construct is present in a concentration range of 0.1-5 mg/ml.

6. The composition according to claim 1, wherein the buffer is selected from the group consisting of potassium phosphate, acetic acid/sodium acetate, citric acid/sodium citrate, succinic acid/sodium succinate, tartaric acid/sodium tartrate, histidine/histidine HCl, glycine, Tris, glutamate, acetate and mixtures thereof.

7. The composition according to claim 6, wherein the buffer is selected from the group consisting of potassium phosphate, citric acid/sodium citrate, succinic acid, histidine, glutamate, acetate and combinations thereof.

8. The composition according to claim 1, wherein the pH of the composition is in the range of 4-7.5.

9. The composition according to claim 1, further comprising one or more excipients selected from the group consisting of sucrose, trehalose, mannitol, sorbitol, arginine, lysine, polysorbate 20, polysorbate 80, poloxamer 188, pluronic and combinations thereof.

10. The composition according to claim 1, further comprising one or more preservatives.

11. The composition according to claim 10, wherein the one or more preservative is selected from the group consisting of benzyl alcohol, chlorobutanol, phenol, meta-cresol, methylparaben, phenoxyethanol, propylparaben and thiomerosal.

12. (canceled)

13. (canceled)

14. (canceled)

15. The composition according to claim 3, wherein the β-cyclodextrin is present in a concentration in the range of 0.5% to 2% (w/v).

16. The composition according to claim 15, wherein the β-cyclodextrin is present in a concentration in the range of 0.8% to 1.5% (w/v).

17. The composition according to claim 5, wherein the bispecific single chain antibody construct is present in a concentration range of 0.2-2.5 mg/ml.

18. The composition according to claim 17, wherein the bispecific single chain antibody construct is present in a concentration range of 0.25-1.0 mg/ml.

19. The composition according to claim 1, wherein the amino acid sequence of the bispecific single chain antibody construct is SEQ ID NO: 174.

20. The composition according to claim 19, wherein the cyclodextrin is sulfobutylether-β-cyclodextrin sodium salt in a concentration of about 1% (w/v) and the buffer is potassium phosphate in concentration of about 10 mM, and wherein the composition further comprises mannitol in a concentration of about 4%, sucrose in a concentration of about 2% (w/v), and polysorbate 80 in concentration of about 0.01% (w/v) at a pH of about 6.0.