WO2008076379A2 - Human antibodies to human delta like ligand 4 - Google Patents

Human antibodies to human delta like ligand 4 Download PDF

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Publication number
WO2008076379A2
WO2008076379A2 PCT/US2007/025653 US2007025653W WO2008076379A2 WO 2008076379 A2 WO2008076379 A2 WO 2008076379A2 US 2007025653 W US2007025653 W US 2007025653W WO 2008076379 A2 WO2008076379 A2 WO 2008076379A2
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WO
WIPO (PCT)
Prior art keywords
antibody
seq
human
ser
hdii4
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Ceased
Application number
PCT/US2007/025653
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English (en)
French (fr)
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WO2008076379A3 (en
WO2008076379A8 (en
Inventor
Nicholas J. Papadopoulos
Joel H. Martin
Eric Smith
Irene Noguera-Troise
Gavin Thurston
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Regeneron Pharmaceuticals Inc
Original Assignee
Regeneron Pharmaceuticals Inc
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Priority to RU2009126766/10A priority Critical patent/RU2448979C2/ru
Priority to NO20092596A priority patent/NO347649B1/no
Priority to EP07862940A priority patent/EP2115003B1/en
Priority to ES07862940T priority patent/ES2386480T3/es
Priority to DK07862940.9T priority patent/DK2115003T3/da
Priority to MX2011006348A priority patent/MX358410B/es
Priority to AU2007334366A priority patent/AU2007334366B2/en
Priority to JP2009541401A priority patent/JP5677744B2/ja
Priority to RS20120366A priority patent/RS52439B/sr
Priority to HRP20120536TT priority patent/HRP20120536T1/hr
Priority to SI200730966T priority patent/SI2115003T1/sl
Priority to MX2009005963A priority patent/MX2009005963A/es
Priority to NZ577616A priority patent/NZ577616A/en
Application filed by Regeneron Pharmaceuticals Inc filed Critical Regeneron Pharmaceuticals Inc
Priority to HK10104569.1A priority patent/HK1138019B/en
Priority to CN2007800460304A priority patent/CN101611055B/zh
Priority to PL07862940T priority patent/PL2115003T3/pl
Priority to CA2672622A priority patent/CA2672622C/en
Priority to KR1020097013986A priority patent/KR101516569B1/ko
Priority to MEP-2009-224A priority patent/ME00812B/me
Priority to BRPI0720021-8A priority patent/BRPI0720021A2/en
Publication of WO2008076379A2 publication Critical patent/WO2008076379A2/en
Publication of WO2008076379A3 publication Critical patent/WO2008076379A3/en
Priority to IL198612A priority patent/IL198612A/en
Publication of WO2008076379A8 publication Critical patent/WO2008076379A8/en
Priority to TNP2009000245A priority patent/TN2009000245A1/fr
Anticipated expiration legal-status Critical
Priority to MA32084A priority patent/MA31092B1/fr
Ceased legal-status Critical Current

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Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K16/00—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies
    • C07K16/18—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans
    • C07K16/22—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against growth factors ; against growth regulators
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K39/00—Medicinal preparations containing antigens or antibodies
    • A61K39/395—Antibodies; Immunoglobulins; Immune serum, e.g. antilymphocytic serum
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K39/00—Medicinal preparations containing antigens or antibodies
    • A61K39/395—Antibodies; Immunoglobulins; Immune serum, e.g. antilymphocytic serum
    • A61K39/39533—Antibodies; Immunoglobulins; Immune serum, e.g. antilymphocytic serum against materials from animals
    • A61K39/39558—Antibodies; Immunoglobulins; Immune serum, e.g. antilymphocytic serum against materials from animals against tumor tissues, cells, antigens
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00—Drugs for immunological or allergic disorders
    • A61P37/02—Immunomodulators
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00—Drugs for immunological or allergic disorders
    • A61P37/02—Immunomodulators
    • A61P37/06—Immunosuppressants, e.g. drugs for graft rejection
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00—Drugs for disorders of the cardiovascular system
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K16/00—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies
    • C07K16/18—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K39/00—Medicinal preparations containing antigens or antibodies
    • A61K2039/505—Medicinal preparations containing antigens or antibodies comprising antibodies
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K2317/00—Immunoglobulins specific features
    • C07K2317/20—Immunoglobulins specific features characterized by taxonomic origin
    • C07K2317/21—Immunoglobulins specific features characterized by taxonomic origin from primates, e.g. man
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K2317/00—Immunoglobulins specific features
    • C07K2317/30—Immunoglobulins specific features characterized by aspects of specificity or valency
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K2317/00—Immunoglobulins specific features
    • C07K2317/30—Immunoglobulins specific features characterized by aspects of specificity or valency
    • C07K2317/33—Crossreactivity, e.g. for species or epitope, or lack of said crossreactivity
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K2317/00—Immunoglobulins specific features
    • C07K2317/30—Immunoglobulins specific features characterized by aspects of specificity or valency
    • C07K2317/34—Identification of a linear epitope shorter than 20 amino acid residues or of a conformational epitope defined by amino acid residues
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K2317/00—Immunoglobulins specific features
    • C07K2317/50—Immunoglobulins specific features characterized by immunoglobulin fragments
    • C07K2317/56—Immunoglobulins specific features characterized by immunoglobulin fragments variable (Fv) region, i.e. VH and/or VL
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K2317/00—Immunoglobulins specific features
    • C07K2317/50—Immunoglobulins specific features characterized by immunoglobulin fragments
    • C07K2317/56—Immunoglobulins specific features characterized by immunoglobulin fragments variable (Fv) region, i.e. VH and/or VL
    • C07K2317/565—Complementarity determining region [CDR]
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K2317/00—Immunoglobulins specific features
    • C07K2317/70—Immunoglobulins specific features characterized by effect upon binding to a cell or to an antigen
    • C07K2317/73—Inducing cell death, e.g. apoptosis, necrosis or inhibition of cell proliferation
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K2317/00—Immunoglobulins specific features
    • C07K2317/70—Immunoglobulins specific features characterized by effect upon binding to a cell or to an antigen
    • C07K2317/73—Inducing cell death, e.g. apoptosis, necrosis or inhibition of cell proliferation
    • C07K2317/732—Antibody-dependent cellular cytotoxicity [ADCC]
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K2317/00—Immunoglobulins specific features
    • C07K2317/70—Immunoglobulins specific features characterized by effect upon binding to a cell or to an antigen
    • C07K2317/73—Inducing cell death, e.g. apoptosis, necrosis or inhibition of cell proliferation
    • C07K2317/734—Complement-dependent cytotoxicity [CDC]
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K2317/00—Immunoglobulins specific features
    • C07K2317/70—Immunoglobulins specific features characterized by effect upon binding to a cell or to an antigen
    • C07K2317/76—Antagonist effect on antigen, e.g. neutralization or inhibition of binding
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K2317/00—Immunoglobulins specific features
    • C07K2317/90—Immunoglobulins specific features characterized by (pharmaco)kinetic aspects or by stability of the immunoglobulin
    • C07K2317/92—Affinity (KD), association rate (Ka), dissociation rate (Kd) or EC50 value

Definitions

  • the antibody or antibody fragment comprises the light chain CDR1 , CDR2 and CDR3 selected from the group consisting of SEQ ID NO:439/441/443; 382/384/386; 791/793/795; and 807/809/811.
  • the invention features a human antibody or antibody fragment comprising a light chain CDR2 encoded by a nucleotide sequence selected from the group consisting of SEQ ID NO:15, 31 , 47, 63, 79, 95, 1 11 , 127, 143, 159, 175, 191 , 207, 223, 239, 255, 271 , 287, 303, 319, 335, 351 , 367, 383, 408, 424, 440, 456, 472, 488, 504, 520, 536, 552, 568, 584, 600, 616, 632, 648, 664, 680, 696, 712, 728, 744, 760, 776, 792, 808, 824, 840, 856, 872, and 888, or a substantially similar sequence having at least 95% homology thereof.
  • X 1 is Ne or Leu
  • X 2 is Trp or Ser
  • X 3 is Tyr, Ala or GIy
  • X 4 is Asp, Ser or Tyr
  • X 5 is GIy or Asp
  • X 6 is Ser, GIy, Thr or VaI
  • X 7 is Asn or Asp
  • X 8 is Lys or Arg
  • the invention features a composition comprising a recombinant human anti-human DII4 antibody and an acceptable carrier.
  • vectors and host cells comprising vectors which contain nucleic acid molecules encoding the human anti-hDII4 antibody of the invention, as well as methods of producing these novel antibodies, comprising growing a host cell comprising nucleic acid encoding the anti-hDII4 antibody of the invention or an antibody fragment, under conditions permitting production of the protein and recovering the protein so produced.
  • antibody is intended to refer to immunoglobulin molecules comprised of four polypeptide chains, two heavy (H) chains and two light (L) chains interconnected by disulfide bonds.
  • Each heavy chain is comprised of a heavy chain variable region (abbreviated herein as HCVR or VH) and a heavy chain constant region.
  • the heavy chain constant region is comprised of three domains, CH1 , CH2 and CH3.
  • Each light chain is comprised of a light chain variable region (abbreviated herein as LCVR or VL) and a light chain constant region.
  • the light chain constant region is comprised of one domain, CL.
  • binding fragments encompassed within the term "antigen-binding portion" of an antibody include (i) a Fab fragment, a monovalent fragment consisting of the VL, VH, CL and CH 1 domains; (ii) a F(ab') 2 fragment, a bivalent fragment comprising two Fab fragments linked by a disulfide bridge at the hinge region; (iii) a Fd fragment consisting of the VH and CH 1 domains; (iv) a Fv fragment consisting of the VL and VH domains of a single arm of an antibody, (v) a dAb fragment (Ward et al.
  • human antibody is intended to include antibodies having variable and constant regions derived from human germline immunoglobulin sequences.
  • the human antibodies of the invention may include amino acid residues not encoded by human germline immunoglobulin sequences (e.g., mutations introduced by random or site-specific mutagenesis in vitro or by somatic mutation in vivo), for example in the CDRs and in particular CDR3.
  • human antibody as used herein, is not intended to include antibodies in which CDR sequences derived from the germline of another mammalian species, such as a mouse, have been grafted onto human framework sequences.
  • surface plasmon resonance refers to an optical phenomenon that allows for the analysis of real-time biospecific interactions by detection of alterations in protein concentrations within a biosensor matrix, for example using the BIACORETM system (Pharmacia Biosensor AB, Uppsala, Sweden and Piscataway, N. J.).
  • K D is intended to refer to the dissociation constant of a particular antibody-antigen interaction.
  • constrained peptides comprising a consensus sequence or a substantially identical consensus sequence variation may be generated by methods known in the art (Rizo et al. (1992) Ann. Rev. Biochem. 61 :387), for example, by adding internal cysteine residues capable of forming intramolecular disulfide bridges which cyclize the peptide.
  • the term "percent sequence identity" in the context of nucleic acid sequences refers to the residues in two sequences which are the same when aligned for maximum correspondence.
  • Methods for generating human antibodies include, for example, VELOCIMMUNE ® (Regeneron Pharmaceuticals), XENOMOUSETM technology (Abgenix), the "minilocus” approach, and phage display.
  • the VELOCIMMUNE ® technology (U.S. 6,596,541) encompasses a method of generating a high specificity fully human antibody to a select antigen. This technology involves generation of a transgenic mouse having a genome comprising human heavy and light chain variable regions operably linked to endogenous mouse constant region loci such that the mouse produces an antibody comprising a human variable region and a mouse constant region in response to antigenic stimulation.
  • the DNA encoding the variable regions of the heavy and light chains of the antibody are isolated and operably linked to DNA encoding the human heavy and light chain constant regions.
  • the DNA is then expressed in a cell capable of expressing the fully human antibody.
  • the cell is a CHO cell.
  • the dimers are not linked via inter-heavy chain disulfide bonds and a molecule of about 75-80 kDa is formed composed of a single light and heavy chain. These forms have been difficult to separate, even after affinity purification.
  • the frequency of appearance of the second form in various intact IgG isotypes is due to, but not limited to, structural differences associated with the hinge region isotype of the antibody.
  • a single amino acid substitution in the hinge region of the human lgG4 hinge can significantly reduce the appearance of the second form (Angal et al. 1993 Molecular Immunology 30:105) to levels typically observed using a human IgGI hinge.
  • the instant invention encompasses antibodies having one or more mutations in the hinge, CH2 or CH3 region which may be desirable, for example, in production to improve the yield, or modulate effector functions.
  • immune cell function or reduction of immune cell numbers can be ameliorated through inhibition of immune cell function or reduction of immune cell numbers.
  • This can be accomplished by blockade of positive signals or stimulation of negative signals on immune cell populations critical to the disease process, such as T, B or NK cells, neutrophils, macrophages, antigen presenting cells, mast cells or other cell types.
  • Overactivity can also be inhibited through elimination of various immune cell populations by stimulation of apoptosis, targeting of specific surface receptors with depleting antibodies or antibody-drug conjugates, or the blockade or alteration of the differentiation of immune cell lineages or specific cell types.
  • Anti-hDII4 antibodies generated via direct isolation of splenocvtes. Antigen-specific antibodies may also be isolated directly from antigen-immunized B cells without fusion to myeloma cells, as described in U.S. Patent Publication 2007/0280945A1. Stable recombinant antibody-expressing CHO cell lines were established from the isolated proper recombinants.
  • biotin-DII4-hFc a constant amount of biotin-DII4-hFc at 25 pM was pre-mixed with varied amounts of antibody, either in crude hybridoma condition medium or as purified antibody protein, ranging from 0 to ⁇ 50 nM in serial dilutions, followed by 2 hr incubation at room temperature to allow antibody-antigen binding to reach equilibrium.
  • the equilibrated sample solutions were then transferred to the Notch-hFc coated plates for the measurement of free biotin-DII4-hFc.
  • Complement-dependent cytotoxicity (CDC) induced by REGN421 was assessed using the same panel of cells lines described above. Briefly, cells from each of the target cell lines (50,000 cells/well in 50 ⁇ l) were first mixed with an equal volume of serially diluted REGN421 , resulting in a final antibody concentration ranging from 0.169 pM to 10 nM, and incubated for 10 min at room temperature in a 96-well plate format. Normal human serum, with complement components (Quidel Corp., San Diego, CA) was added to each well to give a final serum concentration of 5%.
  • the chimeric proteins were fused to a mouse lgG2a-Fc fragment and expressed in CHO-K1 cell. The conditioned media were harvested and protein expression confirmed by western blot. [0095] Binding specificity of test antibodies to hDII4, mDII4, and chimeric proteins #1 , #2, #3, and #4 were tested as follows: purified antibodies 22G12, VAW3A7-2, and 15E10 were amine coupled between 5000- 6000 RU on CM5 chip. Conditioned media from CHO K1 cells containing the chimeric DII4 proteins, hDII4-mFc, and mDII4-mFc were injected sequentially followed by surface regeneration over antibody-coupled surfaces.
  • Example 7 Binding Affinity of Purified Antibodies to Human and Monkey DII4.
  • the binding affinities of selected purified antibodies to hDII4, M. facscicularis DII4 (mfDII4, SEQ IN NO:956), and M. mulatta DII4 (mmDII4, SEQ ID NO:957) monomers were determined using a BIACORE TM 2000 & 3000. Goat anti-hFc polyclonal antibody reagent immobilized on a BIACORETM chip was used to present REGN281 , REGN421 , and REGN422.

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  • Health & Medical Sciences (AREA)
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  • Organic Chemistry (AREA)
  • Medicinal Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Health & Medical Sciences (AREA)
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  • Bioinformatics & Cheminformatics (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Proteomics, Peptides & Aminoacids (AREA)
  • Molecular Biology (AREA)
  • Biochemistry (AREA)
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  • Genetics & Genomics (AREA)
  • Epidemiology (AREA)
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  • Pain & Pain Management (AREA)
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  • Medicines Containing Antibodies Or Antigens For Use As Internal Diagnostic Agents (AREA)
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PCT/US2007/025653 2006-12-14 2007-12-14 Human antibodies to human delta like ligand 4 Ceased WO2008076379A2 (en)

Priority Applications (23)

Application Number Priority Date Filing Date Title
NO20092596A NO347649B1 (no) 2006-12-14 2007-12-13 Humant antistoff eller antistoff fragment som spesifikt binder human deltaliknende ligand 4 (hDII4), nukleinsyremolekyl som koder for slike og vektor og vert-vektorsystemer, samt fremgangsmåte for fremstilling, sammensetning og anvendelse.
RU2009126766/10A RU2448979C2 (ru) 2006-12-14 2007-12-13 Антитела человека к дельта-подобному лиганду-4 человека
HK10104569.1A HK1138019B (en) 2006-12-14 2007-12-14 Human antibodies to human delta like ligand 4
DK07862940.9T DK2115003T3 (da) 2006-12-14 2007-12-14 Humane antistoffer mod human delta-lignende ligand 4
MX2011006348A MX358410B (es) 2006-12-14 2007-12-14 Anticuerpos humanos contra el ligando 4 de tipo delta humano.
AU2007334366A AU2007334366B2 (en) 2006-12-14 2007-12-14 Human antibodies to human delta like ligand 4
JP2009541401A JP5677744B2 (ja) 2006-12-14 2007-12-14 ヒトＤｅｌｔａ様リガンド４に対するヒト抗体
RS20120366A RS52439B (sr) 2006-12-14 2007-12-14 Humana antitela prema humanom delti sličnom ligandu 4
HRP20120536TT HRP20120536T1 (hr) 2006-12-14 2007-12-14 Humana protutijela za humani delta-like ligand 4
SI200730966T SI2115003T1 (sl) 2006-12-14 2007-12-14 Humana protitelesa proti humanemu delti podobnemu ligandu 4
MX2009005963A MX2009005963A (es) 2006-12-14 2007-12-14 Anticuerpos humanos contra el ligando 4 de tipo delta humano.
NZ577616A NZ577616A (en) 2006-12-14 2007-12-14 Human antibodies to human delta like ligand 4
PL07862940T PL2115003T3 (pl) 2006-12-14 2007-12-14 Ludzkie przeciwciała skierowane przeciwko ludzkiemu ligandowi podobnemu do liganda delta 4
EP07862940A EP2115003B1 (en) 2006-12-14 2007-12-14 Human antibodies to human delta like ligand 4
CN2007800460304A CN101611055B (zh) 2006-12-14 2007-12-14 抗人delta样配体4的人抗体
ES07862940T ES2386480T3 (es) 2006-12-14 2007-12-14 Anticuerpos humanos para ligando 4 similar a delta humano
CA2672622A CA2672622C (en) 2006-12-14 2007-12-14 Human antibodies to human delta like ligand 4
KR1020097013986A KR101516569B1 (ko) 2006-12-14 2007-12-14 사람 델타 유사 리간드 4에 대한 사람 항체
MEP-2009-224A ME00812B (me) 2006-12-14 2007-12-14 Humana antitela prema humanom delti sličnom ligandu 4
BRPI0720021-8A BRPI0720021A2 (en) 2006-12-14 2007-12-14 human antibodies to human delta-4-like ligand
IL198612A IL198612A (en) 2006-12-14 2009-05-06 @Human ligand @ ligand @@@ human delta-like method, method of making them, preparations containing them and using them @ making @ drugs
TNP2009000245A TN2009000245A1 (en) 2006-12-14 2009-06-12 Human antibodies to human delta like ligand 4
MA32084A MA31092B1 (fr) 2006-12-14 2009-07-09 Anticorps humains contre le delta-like ligand 4 humain.

Applications Claiming Priority (6)

Application Number Priority Date Filing Date Title
US87492206P 2006-12-14 2006-12-14
US60/874,922 2006-12-14
US91641507P 2007-05-07 2007-05-07
US60/916,415 2007-05-07
US98532307P 2007-11-05 2007-11-05
US60/985,323 2007-11-05

Publications (3)

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WO2008076379A2 true WO2008076379A2 (en) 2008-06-26
WO2008076379A3 WO2008076379A3 (en) 2008-09-18
WO2008076379A8 WO2008076379A8 (en) 2009-05-14

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PCT/US2007/025653 Ceased WO2008076379A2 (en) 2006-12-14 2007-12-14 Human antibodies to human delta like ligand 4

Country Status (33)

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US (9) US7919593B2 (enExample)
EP (2) EP2115003B1 (enExample)
JP (2) JP5677744B2 (enExample)
KR (1) KR101516569B1 (enExample)
CN (1) CN101611055B (enExample)
AU (1) AU2007334366B2 (enExample)
BR (1) BRPI0720021A2 (enExample)
CA (1) CA2672622C (enExample)
CR (1) CR10863A (enExample)
CY (1) CY1113087T1 (enExample)
DK (1) DK2115003T3 (enExample)
DO (1) DOP2009000140A (enExample)
EC (1) ECSP099404A (enExample)
ES (1) ES2386480T3 (enExample)
GT (1) GT200900167A (enExample)
HR (1) HRP20120536T1 (enExample)
IL (1) IL198612A (enExample)
MA (1) MA31092B1 (enExample)
ME (1) ME00812B (enExample)
MX (2) MX2009005963A (enExample)
MY (1) MY164461A (enExample)
NI (1) NI200900115A (enExample)
NO (1) NO347649B1 (enExample)
NZ (1) NZ577616A (enExample)
PL (1) PL2115003T3 (enExample)
PT (1) PT2115003E (enExample)
RS (1) RS52439B (enExample)
RU (1) RU2448979C2 (enExample)
SG (2) SG177189A1 (enExample)
SI (1) SI2115003T1 (enExample)
SV (1) SV2009003296A (enExample)
TN (1) TN2009000245A1 (enExample)
WO (1) WO2008076379A2 (enExample)

Cited By (85)

* Cited by examiner, † Cited by third party
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