NZ739623B2 - Evacuated blood collection tubes containing protease inhibitors for the assessment of contact system activation - Google Patents

Abstract

Disclosed herein are evacuated blood collection tubes comprising protease inhibitor cocktails in liquid form and uses thereof for assessing features associated with the contact system in a subject, including the endogenous level of contact system activation, the endogenous level of a drug that targets a component of contact system during treatment, and/or the immunogenicity of such a drug. In a specific embodiment the invention involves a method for assessing the endogenous level of contact system activation in a subject, the method comprising: collecting blood from a subject to an evacuated blood collection tube; processing the blood to produce a plasma sample; and measuring the level of contact system activation in the plasma sample, wherein the evacuated blood collection tube comprises a liquid formulation comprising a mixture of protease inhibitors, polybrene, and EDTA; wherein the mixture of protease inhibitors comprises benzamidine, soybean trypsin inhibitor, leupeptin, and 4-(2- aminoethyl) benzenesulfonyl fluoride hydrochloride (AEBSF).

Description

EVACUATED BLOOD COLLECTION TUBES CONTAINING PROTEASE INHIBITORS FOR THE ASSESSMENT OF CONTACT SYSTEM ACTIVATION CROSS REFERENCE TO RELATED APPLICATIONS This application claims the benefit of the filing date of U.S. ional Application No. ,644 filed August 13, 2015 and U.S. Provisional Application No. 62/214,308, filed September 4, 2015. The entire contents of each of these referenced applications are orated by reference herein.

BACKGROUND OF THE INVENTION Accurate measurement of the in vivo level of contact system activation using patient plasma is challenging due to the propensity for ex vivo activation during blood collection.

Blood from patients with certain diseases associated with the contact system, e.g., hereditary angioedema, is especially prone to ex vivo contact system activation since it is deficient in C1 inhibitor, the natural inhibitor of the pathway. Consequently, measurements of pathway specific kers (e.g., n high molecular weight kininogen) may overestimate the degree of contact system activation that is present within the t, unless the blood is carefully collected and processed.

SUMMARY OF THE INVENTION The present disclosure is based, at least in part, on the development of non-glass evacuated blood collection tubes containing protease inhibitor mixtures ails) in liquid formulation, which prevents ex vivo activation of the contact system during blood collection.

As such, the evacuated blood collection tubes described herein allow for accurate measurement of the nous level of contact system activation of patients, particularly those who are deficient in a natural tor (e.g., C1 inhibitor) of this pathway.

Accordingly, in a first aspect, the t invention provides a method for ing the endogenous level of contact system activation in a subject, the method comprising: (i) collecting blood from a subject to an evacuated blood collection tube; (ii) processing the blood to produce a plasma sample; and (iii) measuring the level of contact system activation in the plasma sample, wherein the evacuated blood collection tube comprises a liquid formulation comprising a mixture of protease inhibitors, polybrene, and EDTA; wherein the mixture of protease inhibitors comprises benzamidine, soybean trypsin inhibitor, leupeptin, and 4-(2- aminoethyl) benzenesulfonyl de hloride (AEBSF).

In a second aspect, the present invention provides a method for assessing the level of a drug targeting the contact system in a subject, the method comprising: (i) collecting blood from a subject to an evacuated blood collection tube; wherein the subject has been administered with a drug that targets a component of the contact ; (ii) sing the blood to produce a plasma sample; and (iii) measuring the level of the drug in the plasma sample; wherein the evacuated blood collection tube comprises a liquid formulation comprising a mixture of protease inhibitors, polybrene, EDTA; wherein the mixture of protease inhibitors comprises benzamidine, soybean trypsin inhibitor, leupeptin, and 4-(2- thyl) benzenesulfonyl fluoride hydrochloride (AEBSF).

In a third aspect, the t invention provides a method for assessing genicity of a drug ing the t system, the method comprising: (i) collecting blood from a subject to an evacuated blood collection tube; wherein the subject has been administered with a drug that targets a component of the contact system; (ii) processing the blood to produce a plasma sample; and (iii) measuring the level of antibodies that bind to the drug in the plasma sample; wherein the evacuated blood collection tube comprises a liquid formulation comprising a mixture of protease inhibitors, ene, EDTA; wherein the mixture of protease inhibitors comprises benzamidine, soybean trypsin inhibitor, leupeptin, and 4-(2- aminoethyl) benzenesulfonyl fluoride hydrochloride (AEBSF).

One aspect of the present disclosure es an evacuated blood collection tube, comprising a liquid formulation that comprises a mixture of protease inhibitors, which may be ntially free of protease tors that are unstable in an aqueous solution. The tube may be a non-glass tube. In some embodiments, the tube is 1a followed by page 2 plastic. In some ments, the ted blood collection tube contains 0.5 ml of any of the liquid formulations described here, which can be diluted by 10—fold in use.

In some embodiments, the mixture of protease inhibitors in the evacuated blood collection tube described herein comprises at least one serine protease inhibitor (e.g., a plasma kallikrein inhibitor) and at least one cysteine protease inhibitor. In one example, the mixture of protease inhibitors comprises EPI—KALZ, which may be biotinylated, and leupeptin. The amount of EPI—KAL2 may range from 5 to 15 uM in the liquid formulation containing such. Alternatively or in addition, the amount of leupeptin may range from 200 to 300 uM in the liquid formulation.

In some embodiments, the mixture of protease inhibitors described herein may comprise at least two serine protease inhibitors, at least one of which is a trypsin inhibitor, for example, soybean trypsin inhibitor. In some es, the mixture of protease inhibitors ses benzamidine, soybean trypsin inhibitor, leupeptin, and AEBSF. In some examples, the liquid formulation in the evacuated blood collection tube may comprise 80—120 mM benzamidine, 1—3 mg/ml soybean n inhibitor, 200—300 uM leupeptin, and/or 10—30 mM AEBSF.

The liquid ation in any of the evacuated blood collection tubes described herein may further comprise polybrene and EDTA. In some ments, any of the liquid formulations described herein may have a pH of 4—6 (e.g., 4.5).

In another aspect, the present disclosure provides a method for assessing the endogenous level of contact system activation in a subject. The method ses: (i) collecting blood from a subject to any of the evacuated blood collection tubes described ; (ii) processing the blood to produce a plasma sample; and (iii) measuring the level of contact system tion in the plasma sample. In some ments, the measuring step (step (iii)) can be carried out by measuring the level of one or more kers tive of contact system activation. Such biomarkers may comprise prekallikrein, active plasma kallikrein (pKal), OLZM—pKal complex, active factor XII, active factor XI, high molecular weight kininogen (HMWK), and/or a bradykinin metabolite. In one example, the one or more biomarkers comprise cleaved HMWK and/or intact HMWK.

In yet another aspect, the present disclosure provides a method for assessing the level of a drug targeting contact system in a subject. The method comprises: (i) collecting blood from a subject to an ted blood collection tube as described herein, wherein the subject is administered with a drug that targets a component of the contact system; (ii) processing the blood to produce a plasma sample; and (iii) measuring the level of the drug in the plasma sample.

Further, the present disclosure es a method for assessing immunogenicity of a drug ing contact system, the method comprising: (i) collecting blood from a subject to an evacuated blood collection tube as described herein, wherein the subject is administered a drug that targets a component of the contact system; (ii) processing the blood to produce a plasma sample; and (iii) measuring the level of antibodies that bind to the drug in the plasma sample. Such a method may further se, prior to step (iii), isolating antibodies that bind the drug from the plasma sample. In some examples, the anti—drug antibodies (ADAs) can be isolated by a solid phase extraction and acid dissociation (SPEAD) assay.

In any of the s described herein, the subject can be a human patient, who, in some instances, may be treated with a drug targeting a component (e.g., plasma kallikrein) of the contact system, for example, a drug (e.g., an antibody) specifically targeting plasma rein (e.g., the active form of plasma rein). In some examples, the blood is d from a human t having a disease associated with the contact system, e.g., hereditary dema (HAE) or idiopathic angioedema. In some instances, the human patient has HAE with normal C bitor (Cl—INH).

In any of the methods described herein, the evacuated blood collection tube may not be the first tube filled with blood from the subject. Alternatively or in addition, the process step [step (ii)] can be performed within one hour after the blood collecting step [step (i)].

The details of one or more embodiments of the invention are set forth in the description below. Other features or advantages of the present invention will be apparent from the ing drawings and detailed description of several embodiments, and also from the appending claims.

BRIEF DESCRIPTION OF THE DRAWINGS The following drawings form part of the present specification and are included to further demonstrate certain aspects of the present disclosure, which can be better understood by reference to one or more of these gs in combination with the detailed description of ic embodiments presented herein.

Figure l is a photo showing that the SCATl69 and SCAT153 tubes prevented t activation as measured in a 2—Chain Western blot assay. When 10% ellagic acid is added to the plasma, the contact system is activated leading to the conversion of l—chain HMWK to 2— chain HMWK (see the Sodium citrate plasma). In contrast, the SCATl69 and SCAT153 plasma contains the same amount of l—chain HMWK pre— and post—addition of the ellagic acid.

Figure 2 is a graph showing variation of kininogen cleavage (percent 2— HMWK/cHMWK) based on sample collection methods in plasma from healthy subjects. The clinical site of collection, as well as the types of tubes used for collection, is indicated, including KZEDTA (EDTA), sodium citrate, SCATl69, or P100. The groupings of data points correspond to, from left to right, site 1: EDTA, site 2: e; site 3: e, site 4: citrate, site 1: SCATl69, site 2: SCATl69, site 4: 9, site 5: SCATl69, and site 4: P100.

Figure 3 is a graph showing kininogen cleavage (percent 2—HMWK/cHMWK) in plasma ted in SCAT 169 tubes from healthy subjects from different clinical sites. The groupings of data points correspond to, from left to right, site 1: commercial vendor, site 4, site 5, and sites 4 and 5.

Figure 4 is a graph showing kinongen ge (percent 2—HMWK/cHMWK) in healthy subjects as compared to subjects having type I or II HAE, nCl—INH HAE, and idiopathic angioedema (AE). The ngs of data points correspond to, from left to right, healthy subjects, HAE I/II basal, HAE I/II attack, HAE (nCl—INH) basal, HAE (nCl—INH) attack, idiopathic AE basal, and idiopathic AE attack.

Figure 5 is a graph g 2—chain HMWK levels in plasma from healthy ts and patients with HAE. A: shows the tage of plasma 2—chain HMWK levels from healthy subjects. As indicated in the graph, clinical site C did not use an initial discard tube before collection of SCAT169 plasma. B: shows the percentage of plasma 2—chain HMWK levels from patients with HAE.

DETAILED PTION OF THE INVENTION The present disclosure is based, at least in part, on the development of ted blood collection tubes comprising protease tor cocktails that prevent contact system activation. In order to accurately assess the endogenous level of contact system activation in a patient or a healthy volunteer, it is critical that blood is carefully collected and processed.

One or more of the ing tions may be taken to ensure accurate assessment of features associated with the contact system as described herein: (i) The evacuated blood collection tubes described herein are preferred not to be the first tube filled with blood, which can show elevated contact system activation due to the local trauma following vessel puncture by the needle; (ii) The blood may not come into contact with glass (use plastic tubes or catheters); (iii) The blood may be sed to plasma within a short period of time (e.g., ~ 1 hour) after collection; and/or (iv) The use of protease inhibitors in the collection tube may stabilize the plasma against ex vivo contact activation which masks accurate determination of endogenous patient status.

The advantages of the evacuated blood collection tubes described herein include, at least: (I) the use of evacuated non—glass (e.g., plastic) tubes for standardized and simplified blood collection; (2) the use of a liquid formulation comprising the protease inhibitor ils to minimize ysis; (3) optional omission of protease inhibitors that are unstable in aqueous solutions (e.g., PPACK II, also known as e—Phe—Arg— chloromethyl ketone); and (4) inclusion, in some embodiments, a plasma kallikrein inhibitor such as EPI—KAL2 (may be ylated), which offers the ability for the tubes to contain a reagent that permits detection of activated plasma kallikrein using an immunoassay. See, 6. g. the relevant disclosures thereof are incorporated by reference herein.

, WO95/21601, An unexpected observation from this study was that the use of the protease inhibitor il in liquid form prevented or d hemolyzation. When blood was collected into evacuated tubes containing a lyophilized preparation of the protease inhibitors, it was largely hemolyzed, which may interfere with certain analyte measurements. However, when blood is collected into an evacuated tube ning a solution of the same protease tor mixture, it was not hemolyzed.

Consequently, measurements directed at assessing the degree of contact system activation in plasma samples sed from blood samples collected in the evacuated tubes described herein provide more accurate assessment levels from patients with different diseases. ing an accurate estimate of contact activation can allow for identification of diseases or subsets of patients with different diseases that are potentially mediated by this pathway and therefore amenable to treatment with an inhibitor of the contact system.

Further, the use of the evacuated blood collection tubes bed herein can facilitate the accurate determination of drug levels and/or immunogenicity assessment for a therapeutic molecule directed t activated forms of proteins in the contact system (e.g., plasma kallikrein, FXIIa, and 2—chain kininogen). The tubes may offer a similar advantage for therapeutic les targeted to activated proteins downstream of the contact system activation that do not e calcium for the generation of the activated target (e.g., FXIa, and FIXa). The advantage of these tubes primarily applies to biologic therapeutic molecules since the PK and immunogenicity assays used are typically immunoassays that recognize the binding site (e.g., the idiotype, in the case of a therapeutic antibody). If the therapeutic target is activated ex vivo, it can bind the biologic present in the plasma and thereby mask detection in the PK and immunogenicity immunoassays. The protease tors in the tubes can prevent the target activation. The use of the liquid formulation prevents sis, which can ere in certain laboratory .

Evacuated Blood Collection Tubes Containing Protease Inhibitor Cocktails in Liquid Formulation ted blood tion tubes are commonly used in medical practices for collecting blood samples for various uses. The tubes described herein may be non—glass tubes comprising a liquid ation that comprises a mixture of protease inhibitors (a protease tor cocktail). In some embodiments, the protease inhibitor cocktail may comprise at least one serine protease inhibitor and at least one cysteine protease inhibitor. At least one serine protease inhibitor can be a plasma kallikrein inhibitor. Such protease inhibitor cocktails may comprise multiple (e.g., 2, 3, 4, or 5) serine protease inhibitors, at least one of which can be a trypsin or human plasmin inhibitor. Preferably, the protease inhibitor cocktails described herein are ntially free of a protease inhibitor that is unstable in an aqueous solution, i.e., the ty of the protease inhibitor that is unstable in an aqueous solution is insubstantial as relative to the total inhibitory activity of the protease il. In some instances, the amount of the protease inhibitor that is unstable in an aqueous solution may be less than 5% (w/w) of the total protease inhibitors in the cocktail, e.g., less than 2%, less than 1%, or less than 0.5%. In some ces, the protease inhibitor cocktail is completely free of a protease tor that is unstable in an aqueous solution (e.g., an aqueous solution having a pH of 4—6). One example of protease inhibitor that is not stable in an aqueous solution is PPACK II, also known as H—D—Phe—Phe—Arg—chloromethyl ketone.

Table 1 below lists exemplary serine protease inhibitors, ne protease inhibitors, and trypsin protease inhibitors, which can be used for making the protease inhibitor cocktails described herein.

Exemplary tors Serine Protease * Benzamidine Inhibitors * 4-(2-Aminoethyl) benzenesulfonyl ?uoride hydrochloride (AEB SF); * * Chymostatin; * Nalpha-Tosyl-Lys methyl Ketone (TLCK); * Tos-Phe-CH2C1; N-p-Tosyl-L-phenylalanine Chloromethyl ketone (TPCK) * l-({(6R,7S)[(acetyloxy)methyl]methoxy-5,5-dioxidooxo thia-l -azabicyclo[4.2.0]octenyl } carbonyl)-L-proline * Patamostat mesylate; *Gabexate mesylate; * ck (Meosuc-aapv-cmk; MeOSuc-Ala-Ala-Pro-Val-CMK) * Nafamostat mesylate; * Rosmarinic acid; * Purpurogallin; * 2-(4-((l-Acetimidoyl-3 -pyrrolidinyl)oxy)phenyl)-3 idino naphthyl)propanoic acid hydrocloride ydrate * 4-(4-Bromophenylsulfonylcarbamoyl)benzoyl-L-valyl-L-proline- 1 (RS)- (l-tri?uoroacety1methylprolyl)amide *L-658758; CHEMBL446371; L 658758 * Sivelestat; * Patamostat; * Cholesterol e; * Elastase Inhibitor III; * Gabexate; * 4',6-Dian1idinophenylindole; * nobenzan1idine; * 3,4-dichloroisocoumarin; * Bivalirudin Tri?uoroacetate * Pradaxa; * HIRUDIN; * Ximelagatran; * Lepirudin; Re?udan; wa 023 Bivalirudin; Letaxaban; Eribaxaban; tran ate mesylate; Apixaban; Tanexaban; Rivaroxaban; Xarelto; 3667898 * Plasma kallikrein inhibitors such as EPL-KALZ, DX-88, DX-2930, etc.

Thefollowing examples are n and/0r human plasmin inhibitors: * Soybean trypsin tor * 4-(2-an1inoethyl)benzenesulfonyl?uoride * 4-an1inobenzan1idine * alpha I-Antitrypsin * Aprotinin * Camostat * Eco protein (E coli) * inter-alpha-inhibitor * Nafamostat * NCO 650 * Ovornucin * Somatornedin B * Trypsin Inhibitor (Bowman-Birk Soybean) * Trypsin Inhibitor (Kunitz Soybean) * Urinastatin Cysteine Protease * Geldanamycin; 305626; AKOSO22185390 Inhibitor * Calpastatin; * L-Proline,N-[[(2S,3S) [(Propylan1ino)carbonyl] oxiranyl]carbony1] L-isoleucyl-; * Proteasome Inhibitor I; * (Ltrans-(Propylcarbarnyl)oxiranecarbony1)-L-isoleucyl-L-proline; * Calpain Inhibitor III; * rans-(Propylcarbamoyl)oxiranecarbonyl]-L-isoleucy1-L- proline; * Ornuralide; * (S)-MG132; * Lactacystin; * Z-Phe-ala-diazomethane; * Leupeptin; * 4-Hydroxynonenal; * trans-Epoxysuccinyl-L-leucylamido(4-guanidino)butane; * Loxistatin; * Clasto-lactacystinbeta-lactone; * L-Proline, * Z-FA-FMK; * N-acetylleucyl-leucyl-methioninal; * nitroaspirin; * Allnal; * tatin; * ethyl 3-( { 4-methyl-l -[(3 lbutyl)amino] - l -oxopentan yl } carbamoyl)oxiranecarboxylate; * (+/—)4-HYDROXYNONENAL; In some examples, the protease inhibitor cocktail for use in making the evacuated blood collection tubes comprises at least one serine protease inhibitor (e.g., 1, 2, or 3), which may include at least one trypsin/plasmin inhibitor (e.g., 1, 2, or 3), and at least one cysteine protease inhibitor (e.g., 1, 2, or 3). Such a protease inhibitor cocktail may comprise three serine protease tors (e.g., benzamidine, AEBSF, and a trypsin/plasmin inhibitor such as soybean trypsin inhibition) and one ne protease tor (6.g. , tin).

In other examples, the protease inhibitor cocktail may comprise at least one serine protease inhibitor (6.g. , a plasma ka11ikrein inhibitor) and at least one cysteine protease inhibitor (e.g., leupeptin). The plasma kalikrein inhibitor may be EPI—KAL2 (Met His Ser Phe Cys Ala Phe Lys Ala Asp Asp Gly Pro Cys Arg Ala Ala His Pro Arg Trp Phe Phe Asn Ile Phe Thr Arg Gln Cys Glu Glu Phe Ser Tyr Gly Gly Cys Gly Gly Asn Gln Asn Arg Phe Glu Ser Leu Glu Glu Cys Lys Lys Met Cys Thr Arg Asp; SEQ ID NO: 1), which is a specific plasma ka11ikrein, recombinant protease inhibitor that offers the ability for the tubes to contain a reagent that permits detection of activated plasma ka11ikrein using, e.g., immunoassays.

Any of the protease inhibitor cocktails may be dissolved in a suitable solution to form a liquid formulation. The le on may be an acid—citrate—dextrose solution, which may comprise trisodium citrate, citric acid, and dextrose. The solution may have a pH value of about 4—6, 4—5, 4.5—5.0, or 42—47, e.g., 4.5. In some embodiments, the solution has a pH value of about 4.0, 4.1, 4.2, 4.3, 4.4, 4.5, 4.6, 4.7, 4.8, 4.9, 5.0, 5.1, 5.2, 5.3, 5.4, 5.5, 5.6, 5.7, .8, 5.9, or 6.0. In some embodiments, the solution has a pH value of about 4.5. The liquid formulation may further se a cationic polymer such as hexadimethrine bromide molecule (polybrene®), which can reduce contact system activation by interaction with negatively d surfacesand a chelating agent (e.g., EDTA), which can inhibit metalloproteases.

The concentration of each of the protease inhibitors in the cocktail may be 5X or 10X higher than the final concentration of such an inhibitor for use in inhibiting the corresponding protease, depending upon the dilution fold in practice. The final concentration of a specific commercially protease inhibitor was known in the art and can be obtained from manufacturer’s protocol. In some es, the concentration of EPI—KAL2 may range from —15 uM (e.g., 5—10, 7 to 12 uM, or 10—15 uM). In some embodiments, the concentration of EPI—KAL2 is about 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, or about 15 MM. In some examples, the concentration of leupeptin may range from 200—300 uM (e.g., 200—250, 240—270, or 250—300 uM). In some embodiments, the concentration of tin is about 200, 210, 220, 230, 240, 250, 260, 270, 280, 290, or about 300 MM. In some examples, the concentration of soybean trypsin inhibitor may range from 1—3 mg/ml (e.g., 1—2 or 2—3 mg/ml). In some embodiments, the concentration of soybean n inhibitor is about 1, 1.2, 1.3, 1.4, 1.5, 1.6, 1.7, 1.8, 1.9, 2.0, 2.1, 2.2, 2.3, 2.4, 2.5, 2.6, 2.7, 2.8, 2.9, or about 3.0 mg/mL. In some es, the concentration of benzamidine can range from 80—120 mM (e.g., 80—100 or 100—120 mM). In some embodiments, the tration of benzamidine is about 80, 85, 90, 95, 100, 105, 110, 115, or about 120 mM. In some examples, the concentration of AEBSF may range from 10— mM (e.g., 10—20 or 20—30 mM). In some embodiments, the concentration of AEBSF is about 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 26, 27, 28, 29, or about 30 When a peptide—based protease inhibitor (e.g., EPI—KAL2) is used, it may be biotinylated following conventional methodology. For e, the peptide inhibitor may be biotinylated as follows. Brie?y, the peptide tor can be dissolved in a suitable solution, such as phosphate—buffered saline (PBS). Freshly prepared Sulfo—NHS—LC—Biotin can be added to the peptide inhibitor solution and incubated on ice for a le period of time.

Excess non—reacted and hydrolyzed biotin can be removed using a spin—desalting column.

The labeling of the peptide inhibitor can be confirmed by ELISA and the protein tration can be determined, for example, by the Bradford assay.

Any of the liquid formulations described herein can be prepared by routine methods, e.g., dissolving the proper components into a suitable solution, and placed in evacuated blood tion tubes, which preferably is ass. The tubes may be stored at —20° C and may be thawed on ice or at refrigerated atures (e.g., about 4°C), such as in a refrigerator within a suitable period of time prior to use.

Utilities of Evacuated Blood tion Tubes Comprising Protease Inhibitor Cocktails in Liquid Form Any of the evacuated blood collection tubes described herein can be used to collect blood samples from subjects for use in ing endogenous features ated with the t system, including, but not limited to, the level of t system activation, the serum level of a drug that targets a component of the contact system, and/or the immunogenicity of such a drug. To reduce ex vivo tion of the contact system (e.g., by local trauma following vessel puncture by the needle), the evacuated blood collection tubes described herein may not be the first tube filled with blood when drawing blood from a subject. For example, the initial blood from the subject may be collected in a first tube, which may be discarded, and then the evacuated blood tion tubes are used to collect the subsequent blood samples, which can be used for analysis. The first tube may be a regular blood collection tube used in routine practice.

After blood collection, the blood samples may be processed to produce plasma s within a suitable period of time (e.g., not exceeding an hour). The plasma samples can be subject to further analysis to assess features associated with the contact system of the subject from whom the initial blood sample is obtained.

The blood samples may be collected from a subject in need of the analysis as described herein. In some instances, the subject is a human patient, who may have, be suspected of having, or be at risk for a disease associated with the contact system. For example, the human patient may have a prior occurrence of HAE or may be at risk for HAE.

The human patient may have type I or type II HAE, who either is deficient in C l—INH or produces an atypical Cl—INH. Alternatively, the human patient may have type III HAE, which is not connected with Cl—INH deficiency. In other examples, the human patient may have a prior occurrence of idiopathic angioedema or may be at risk for idiopathic dema. Such a human patient may have been treated previously or be in the course of ent with a drug that targets a component of the contact system (e. g., pKal or FXIIa or high molecular weight kininogen). i. Assessing Endogenous Level of Contact System Activation In one aspect, the plasma samples noted herein can be analyzed to assess the endogenous level of contact system tion of a subject, which maybe a human patient having, suspected of having, or at risk for a disease associated with the contact system (e. g., HAE or idiopathic angioedema). Such a human patient may be on a treatment of the disease, for e, a treatment involving a pKal inhibitor (e. g., an anti—pKal antibody). In other instances, such a human t may be free of such a treatment. Alternatively, the human subject may be a healthy subject having no such diseases.

The level of contact system activation of the plasma sample can be ined by measuring one or more biomarkers indicative of contact system activation.

Plasma kallikrein (pKal) is the primary bradykinin—generating enzyme in the circulation. The activation of pKal can occur via the contact system or via Factor XIIa, both of which have been linked to e pathology associated with tary angioedema (HAE). Plasma kallikrein circulates as an inactive zymogen called prekallikrein that is mostly bound to its substrate high molecular weight kininogen (HMWK). In response to a stimulus, prekallikrein is cleaved to form active plasma kallikrein. This activation of rein can be mediated, e.g., by Factor XIIa after activation of FXII to FXIIa, or by an effector of the contact cascade. Approximately 75—90% of circulating likrein is bound to HMWK through a tive site interaction with domain 6 of HMWK that will hydrolyze additional molecules of HMWK to generate cleaved HMWK and bradykinin. Active plasma kallikrein cleaves HMWK at two sites, resulting in the release of Bradykinin, a key mediator of pain, in?ammation, edema and angiogenesis. The other cleavage product, d kininogen, comprises to amino acid chains held together by a disulfide bond. Cugno et al., Blood (1997) 89:3213—3218.

Exemplary biomarkers that can be used to assess the level of contact system activation in a patient blood sample (thus determining whether the patient has an elevated level and/or ty of the contact system, e.g., an ed level or activity of pKal), are provided in Table 2 below: Table 2. Contact System Biomarkers Basal Level in HAE A ting or during Biomarker Assay patient relative to normal acute edema attack Prekallikrein ELISA or enzyme Unchanged (~500 nM) or Decreased further activity assay slightly decreased Active pKal ELISA or enzyme Unchanged or slightly Increased ty increased a2M-pKal complex ELISA Elevated, if recent attack Increased Cl INH-pKal ELISA Elevated, if recent attack Increased com I lex FXIIa ELISA or enzyme Unchanged or slightly Increased activity increased FXIa ELISA or enzyme Unchanged or slightly Increased activity increased Intact HMWK ELISA Unchanged or slightly Decreased decreased Cleaved HMWK ELISA Unchanged or slightly Increased increased Bradykinin ELISA or LC-MS Unchanged or slightly sed metabolite increased One or more of the biomarkers indicative of contact system activation may be ed using convention methods. One particularly suitable type of assay for detecting, either qualitatively, semi—quantitatively, or quantitatively, is immunoassays. An immunoassay is any assay in which a target molecule (e.g., a ker le associated with contact system activation) is detected and/or quantified by using a binding agent as described herein that specifically binds the target molecule. The binding agent may be an antibody, which can be a full—length antibody or an antigen—binding fragment thereof. The immunoassay may be a competitive or a non—competitive immunoassay, and may be a homogeneous or a heterogeneous immunoassay. For example, the immunoassay for detecting a contact system biomarker may be an enzyme immunoassay (EIA), radioimmunoassay (RIA), mmunoassay (FIA), chemiluminescent immunoassay (CLIA), counting immunoassay (CIA), immunoenzymometric assay , enzyme—linked immunosorbent assay ), a lateral ?ow immunoassay, a sandwich immunoassay, an immuno—PCR assay, a proximity ligation assay, a western blot assay, or an immunoprecipitation assay. Additional suitable immunoassays for detecting a biomarker provided herein will be apparent to those of skill in the art. It will be apparent to those of skill in the art that this disclosure is not limited to assays, however, and that detection assays that are not based on an antibody or an antigen binding antibody fragment, such as mass ometry, are also useful for the ion and/or quantification of contact system biomarkers as provided herein.

The type of detection assay used for the detection and/or quantification of a contact system biomarker such as those provided herein will depend on the particular situation in which the assay is to be used (e.g., clinical or ch applications), and on the kind and number of biomarkers to be detected, and on the kind and number of t samples to be run in parallel, to name a few parameters. For example, elevated levels of cleaved kininogen (2—chain kininogen) can be detected in plasma samples collected from HAE patients or healthy ts during an acute HAE episode using a Western blot assay. While Western blot assays allow for the simultaneous analysis of contact system kers in a plurality of samples, they are limited in the number of biomarkers that can be assessed in parallel.

Accordingly, in some embodiments, where a plurality of contact system biomarkers provided herein is ed in a single sample, or in multiple samples, assays suitable for such multiplex analysis are preferred. Examples for such assays include, without tion, peptide microarrays and lab—on—a—chip assays, which have been designed to offer a high throughput, multiplex—ready alternative to less scalable immunoassays such as Western blots.

In some examples, a plasma sample can be placed in a multi—well microplate in the presence or e of a pKal inhibitor and/or a contact system activator. The mixture can be ted on ice in the presence of a labeled peptide substrate of pKal for a suitable period of time (e.g., 2 minutes), and corn trypsin inhibitor (CTI) can be added to the mixture to stop the activation reaction. The e can be diluted if necessary and the proteolytic activity can be determined by measuring the level of a ?uorescent peptide ate. The results obtained form such an assay can be relied on to determine the endogenous level of contact system activation of the subject from whom the plasma sample is obtained. They also can be relied on to determine the inhibitory activity of the pKal inhibitor, if used. ii. Assessing Endogenous Levels ofDrugs Targeting the Contact System Another aspect of the t disclosure ns to the use of the evacuated blood collection tubes bed herein for the determination of the levels of a drug targeting a component of the contact system. Drug levels are required to evaluate pharmacokinetic parameters. For example, if the contact system is activated ex vivo in plasma samples collected for the determination of amount of a plasma kallikrein inhibitor (e.g., DX—2930) in plasma, then the excess activated plasma kallikrein could bind the drug and thereby mask its detection in an assay. Any of the evacuated blood collection tubes described herein can be used to more accurately estimate drug levels, for example in a sample collected from a subject.

To practice this method, plasma samples derived from a subject (e.g., a human patient) treated with a drug that targets a component of the contact system (e.g., pKal) may be ed from blood samples collected in the evacuated blood collection tubes described herein following the methods also described . The level of the drug in the plasms sample can be measured following routine practice. In some instances, the drug level can be measured by an assay, e.g., those bed herein. iii. Assessing Immunogenicity ofDrugs Targeting the Contact System Another aspect of the present disclosure pertains to the use of the evacuated blood tion tubes for the determination of the immunogenicity of a biologic inhibitor t a component of the contact system (e. g., pKal). For example, it is common practice to develop immunogenicity assays that are able to measure dies against the drug ("ADAs") in the presence of excess drug in the plasma of the circulation. This requirement for an genicity assay that can measure ADAs is certainly the case for therapeutic monoclonal antibodies, which can have le week half—lives and high drug levels in the circulation. To overcome the interference due to excess drug in the sample, techniques are performed to separate anti—drug antibodies from the drug. Such anti—drug antibodies may be isolated by solid phase extraction and acid dissociation (SPEAD), which involves incubation of a biotinylated form of the drug with the plasma sample for an extended period of time (usually overnight) followed by isolation of the biotinylated drug that may be bound to anti— drug dies using a streptavidin coated plate. The plate is then treated with acid to release the anti—drug antibodies. The released antibodies may be coated directly on another assay plate for ion. In the absence of protease tors in the tion tubes, the t system can become activated ex vivo, leading to the production of active plasma rein. After the acid releasing and re—coating steps noted above, both active pKal and anti—drug antibodies would bind to the surface of the plate. The anti—drug antibody is lly detected using a labeled drug, which could also bind to active pKal, if present, resulting in a false positive signal in the ADA assay.

The use of the evacuated blood collection tubes that comprise the protease inhibitor cocktails described herein can prevent this false positive signal.

General Technigues The practice of the present invention will employ, unless otherwise indicated, conventional techniques of molecular biology (including recombinant techniques), microbiology, cell biology, biochemistry and immunology, which are within the skill of the art. Such techniques are explained fully in the literature, such as, Molecular Cloning: A Laboratory Manual, second edition (Sambrook, et al., 1989) Cold Spring Harbor Press; Oligonucleotide Synthesis (M. J. Gait, ed., 1984); Methods in Molecular Biology, Humana Press; Cell Biology: A Laboratory Notebook (J. E. Cellis, ed., 1998) Academic Press; Animal Cell Culture (R. I. Freshney, ed., 1987); uction to Cell and Tissue Culture (J. P. Mather and P. E. Roberts, 1998) Plenum Press; Cell and Tissue Culture: Laboratory Procedures (A.

Doyle, J. B. Griffiths, and D. G. Newell, eds., 1993—8) J. Wiley and Sons; Methods in Enzymology mic Press, Inc.); Handbook of Experimental Immunology (D. M. Weir and C. C. Blackwell, eds.); Gene Transfer s for ian Cells (J. M. Miller and M.

P. Calos, eds., 1987); Current Protocols in Molecular y (F. M. Ausubel, et al., eds., 1987); PCR: The Polymerase Chain Reaction, (Mullis, et al., eds., 1994); Current Protocols in Immunology (J. E. Coligan et al., eds., 1991); Short Protocols in Molecular Biology (Wiley and Sons, 1999); Immunobiology (C. A. Janeway and P. Travers, 1997); Antibodies (P. Finch, 1997); Antibodies: a cal approach (D. Catty., ed., IRL Press, 1988—1989); Monoclonal antibodies: a practical approach (P. Shepherd and C. Dean, eds., Oxford University Press, 2000); Using antibodies: a laboratory manual (E. Harlow and D. Lane (Cold Spring Harbor Laboratory Press, 1999); The Antibodies (M. Zanetti and J. D. Capra, eds., Harwood Academic Publishers, 1995).

Without further elaboration, it is believed that one skilled in the art can, based on the above description, utilize the present ion to its fullest extent. The ing specific embodiments are, therefore, to be construed as merely illustrative, and not limitative of the remainder of the sure in any way whatsoever. All publications cited herein are incorporated by reference for the purposes or subject matter referenced herein.

Example 1: Preparation of Protease Inhibitor Cocktails that Prevent Contact System Activation Protease inhibitor cocktails that prevented contact system activation were ped.

Evacuated plastic tubes were used for standardized and simplified blood collection.

The ing two protease inhibitor cocktails were utilized in a liquid formulation to prevent hydrolysis: 1) 10X Protease tor Cocktail A: SCAT169 ted 5 mL total volume plastic tubes containing (0.5 ml): 100 mM benzamidine, 400 ug/mL polybrene, 2 mg/mL n trypsin tor, 20 mM EDTA, 263 uM tin, and 20 mM AEBSF (4—(2—Aminoethyl) benzenesulfonyl ?uoride hydrochloride) dissolved in acid—citrate—dextrose (100 mM trisodium citrate, 67 mM citric acid, and 2% dextrose, pH 4.5.). 2) 10X Protease Inhibitor Cocktail B: 3 Evacuated 5 ml total volume c tubes containing (0.5 ml): 10 uM biotinylated EPI—KAL2, 400 ug/mL polybrene, 20 mM EDTA, and 263 uM leupeptin, dissolved in acid—citrate—dextrose (100 mM trisodium citrate, 67 mM citric acid, and 2% dextrose, pH 4.5.).

Biotinylated EPI—KAL2 was included in the Protease Inhibitor Cocktail B (SCAT153). SCAT169 (Specialized Coagulation Assay Tubes, formulation 169) and SCAT153 (Specialized Coagulation Assay Tubes, formulation 153) tubes were stored at 2—8 Example 2: SCAT169 and SCAT153 Tubes Prevent t System tion as Shown By 2-Chain Western Blot Assay Plasma collected in either the SCAT169 or the SCAT153 tubes blocked contact system activation induced by ex vivo addition of ellagic acid (Figure I), a well—known contact system activator, as measured by the conversion of I—chain to 2—chain HMWK by Western blot is.

Observed ellagic nduced contact system activation was compared n plasma samples collected in 3 different blood collection tubes: sodium citrate tubes (standard tubes used in clinical chemistry labs for coagulation ements), SCAT169 tubes, and SCAT153 tubes. n HWMK was essentially completely consumed in sampled activated with ellagic acid in sodium citrate tubes, and the appearance of 2—chain HMWK was detected.

In contrast, I—chain HMWK was ved in ellagic acid—activated plasma from SCAT169 and SCAT153 tubes.

These results ed evidence that the SCAT169 and SCAT153 tubes are effective in preventing ex vivo contact system activation that can occur during plasma sample collection and processing.

Example 3: SCAT169 and SCAT153 Protease Inhibitor Cocktails Increased Plasma Clotting Times Plasma clotting times were measured in samples treated in 3 different blood collection tubes: sodium citrate tubes, SCAT169 tubes, and SCAT153 tubes, for three individual donor samples (Table 1).

As shown through prothrombin and activated partial thromboplastin, clotting time sed in samples with SCAT159 and SCAT153 as compared to sodium citrate. The results are provided in Table 3 below.

Table 3. Effect of the Protease Inhibitors on Plasma Clotting Times Prothrombin Time (s) Activated Partial Thromboplastin Time (s) DONOR#: Example 4: Use of Evacuated Blood Collection Tubes for Assessing Endogenous Levels of Contact System Activation in Human Subjects Examination of plasma biomarkers of contact system activation is challenging due to inadvertent activation during blood collection and processing. In this study, the utility of specialized blood collection tubes (SCAT159 and SCAT153) in assessing levels of cleaved olecular—weight kininogen (cHMWK) in plasma from healthy subjects and those with Types I/II hereditary angioedema (HAE), idiopathic angioedema or HAE with normal C1— INH (HAEnCl, also referred to as nCl—INH) was investigated as follows.

To avoid artificial activation of the contact pathway during blood sampling, the study used standardized blood collection techniques and custom tubes containing protease inhibitors. Blood samples were collected from healthy subjects and the disease subjects noted above g periods of e quiescence and ?are) to assess the percentage of cHMWK using a Western blot assay. The blood samples were placed in SCAT159 or SCAT153 tubes (5 mL total volume, 0.5 mL 10X protease tor cocktail) using a catheter with a butter?y— type needle system. The blood s were then processed to produce plasma samples within 1 hour after blood tion.

The SCAT tube plasma samples were analyzed by Simple Western (SBHD) and Western blot (TGA) to determine the level of cleaved kininogen (2—chain kininogen) in the plasma samples following methods disclosed in, e.g., Plasma was collected from the y ts at clinical sites 1—5 into c collection tubes containing various anti—coagulants, protease inhibitors, or protein stabilizers before being processed to plasma. Specifically, the types of tubes were KZEDTA, sodium citrate, SCAT169 or P100 (BD Biosciences). As shown in Figure 2, the tubes that were found to ze ex vivo contact system activation contained protease inhibitors and were either P100 tubes or SCAT169 tubes, which were 5 mL volume plastic evacuated blood collection tubes containing 0.5 mL 10X concentrated mixture of 100 mM benzamidine, 400 ug/mL ene, 2 mg/mL soybean trypsin inhibitor, 20 mM EDTA, 263 uM leupeptin, and mM AEBSF ved in acid—citrate—dextrose (100 mM ium citrate, 67 mM citric acid, and 2% dextrose, pH 4.5). Collection methods using tubes containing the protease inhibitor cocktails prevented elevation of cHMWK when healthy volunteer plasma was assayed.

Results obtained from this study showed that, in healthy subjects, levels of cHMWK were stable (<5%) at room temperature (RT) for at least 24 hours following blood collection into custom tubes, but the levels of cHMWK were ed (12%) in plasma samples obtained from a cial vendor, demonstrating the importance of optimizing blood collection techniques when examining contact pathway activation. protease The effects of kininogen cleavage in plasma collected into SCAT169 tubes from healthy subjects from two two different clinical sites (sites 4 and 5) and from a commercial vendor (site 1) was also evaluated (Figure 3). The commercial vendor collected blood samples directly into the SCAT 169 tubes wihout an initial discard tube.

Kininogen cleavage was also evaluated in blood samples ted in SCAT169 tubes from ts having types of angioedema (type I/II HAE, nCl—INH HAE, and idiopathic AE). Plasma was collected from healthy subjects or subjects having various types of angioedema in both the quiescent state (basal) and during an attack (attack) to measure the amount of cHMWK in various disease states. cHMWK percentages were clearly elevated at baseline in subjects with HAE (n=21) compared to healthy controls (n=26) but not in plasma from subjects with idiopathic dema (n=4) or HAEnCl (n=5) (Figure 4), suggesting limited plasma rein activity, gh not excluding a role of contact pathway tion during acute attacks in those disorders.

Plasma evaluated for detection of cHMWK is vulnerable to contact system activation stimulated by the collection methods and tubes. In sum, this study provides a refined method for collection of plasma samples for tion of contact system activation, which prevents cleavage of HMWK ex vivo.

Example 5: Use of Evacuated Blood Collection Tubes for Assessing Endogenous Levels of Contact System Activation in Human Subjects The specialized blood collection tubes (SCAT159 and SCAT153) were evaluated for utility in assessing levels of cleaved olecular—weight kininogen (CHMWK) in plasma from healthy subjects and those with Types I/II hereditary angioedema (HAE). , blood samples were collected from the healthy subjects and from patients having HAE, during periods of disease quiescence (basal) and ?are k). The percentage of 2—chain HMWK in the plasma was detected using a Western blot assay. Plasma samples were collected from a phase 1b multicenter, double—blind study of randomized patients with HAE type I/II who received 2 subcutaneous doses of anti—pKal dy (DX—2930) on days 0 and 15 in close groups of 30, 100, 300, or 400 mg or placebo. Blood samples were ed prior to and after the anti—pKal antibody (DX—2930) on days 1, 8, 22, 64, 92, and As shown in Figure 5A, the percentage of plasma 2—chain HMWK levels in samples from y subjects collected from three different clinical sites (A, B, and C) varied with the collection method and type of tube used. Samples using sodium e tubes had higher levels of 2—chain HMWK, relative to samples in SCAT169 tubes. Notably, samples collected at clinical site C, which were collected directly into the SCAT169 tubes and did not use a discard tube prior to the tube containing the protease tor cocktail, had higher levels of 2—chain HMWK as compared to samples using a discard tube.

Similarly, as shown in Figure 5B, the percentage of plasma 2—chain HMWK levels in samples from HAE were higher in the sodium citrate tubes as compared to plasma collected in SCAT169 tubes, likely due to exogenous activation of the contact system associated with plasma collection and processing.

This study demonstrates the advantages of using the blood collection tubes containing the protease inhibitor cocktails, as described , and provides a refined method for collection of plasma samples for evaluation of contact system activation, which prevents aberrant t system tion (e.g., shown by the cleavage of HMWK) ex vivo.

Example 6: Use of Evacuated Blood Collection Tubes for Assessing Plasma Drug Levels Blood is drawn from HAE patients treated with DX—2930 and healthy controls by routine practice and placed into collection tubes. After placing the initial blood s in one or multiple collection tubes, 5 ml of the following blood sample is placed into SCAT159 or SCAT153 tubes. The blood samples are then processed to produce plasma samples within 1 hour after blood collection.

The amount of DX—2930 in the SCAT plasma samples are measured by standard immunoassays, for example, ELISA. Brie?y, a Fab version of an anti—idiotypic onal dy against DX—2930 is coated onto the surface of a 96—well plate overnight and unbound diotypic Fab molecules are d by washing the plate le times. The SCAT plasma samples are then added to the plate, which is incubated at room temperature for 2—3 hours. The plate is washed several times and a biotinylated IgG version of an anti— idiotypic monoclonal antibody t DX—2930 is added to the plate followed by an incubation step and a wash step. Horseradish peroxidase conjugated streptaVidin is then added to the plate. After a 30’ incubation, the plate is washed again and examined for a signal released by the dye. The intensity of the signal corresponds to the amount of 0 in the plasma sample.

Example 7: Use of Evacuated Blood Collection Tubes for Assessing Drug Immunogenicity Plasma samples from HAE patients treated with DX—2930 are prepared from blood samples ted in SCAT159 or SCAT153 tubes, as disclosed above. Anti—DX—2930 antibodies in the plasma sample are isolated by solid phase extraction and acid iation (SPEAD).

Briefly, the plasma samples are incubated with ylated DX—2930 and incubated overnight. The mixture is then placed into a plate coated with streptaVidin to capture biotinylated DX—2930, which bind to anti—DX—2930 antibodies in the plasma sample, if any.

The anti—DX—2930 antibodies are then released by acid treatment and coated directly on a Meso Scale Discovery (MSD) plate. Ruthenium—labled DX—2930 is added to the MSD plate and an electrochemiluminescent signal is ed to detect the ce of anti—DX—2930 antibodies.

OTHER EMBODIMENTS All of the features disclosed in this specification may be combined in any combination. Each feature disclosed in this specification may be replaced by an alternative feature g the same, equivalent, or similar purpose. Thus, unless expressly stated otherwise, each feature disclosed is only an example of a generic series of equivalent or similar es.

From the above description, one skilled in the art can easily ain the essential characteristics of the present invention, and without departing from the spirit and scope thereof, can make various changes and modifications of the invention to adapt it to various usages and ions. Thus, other embodiments are also within the claims.

EQUIVALENTS AND SCOPE 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 present disclosure described herein. The scope of the present disclosure is not ed to be limited to the above description, but rather is as set forth in the appended claims.

In the claims articles such as 6‘ :9 en a an," and "the" may mean one or more than one unless indicated to the contrary or otherwise evident from the context. Claims or descriptions that include "or" between one or more members of a group are considered ied if one, more than one, or all of the group members are present in, employed in, or otherwise relevant to a given product or process unless indicated to the ry or otherwise evident from the context. The present disclosure includes embodiments in which exactly one member of the group is present in, employed in, or otherwise relevant to a given product or process. The present disclosure includes embodiments in which more than one, or all of the group members are present in, employed in, or otherwise relevant to a given product or process.

Furthermore, the present disclosure encompasses all variations, combinations, and permutations in which one or more limitations, elements, clauses, and descriptive terms from one or more of the listed claims is introduced into another claim. For example, any claim that is dependent on another claim can be modified to include one or more limitations found in any other claim that is dependent on the same base claim. Where elements are presented as lists, e.g., in Markush group format, each subgroup of the elements is also disclosed, and any element(s) can be removed from the group. It should it be understood that, in general, where the present disclosure, or aspects of the present disclosure, is/are referred to as comprising particular elements and/or features, certain embodiments of the present disclosure or aspects of the t disclosure consist, or consist essentially of, such elements and/or features. For purposes of simplicity, those embodiments have not been ically set forth in haec verba herein. It is also noted that the terms "comprising" and "containing" are intended to be open and permits the inclusion of additional elements or steps. Where ranges are given, endpoints are included. Furthermore, unless otherwise indicated or otherwise evident from the context and tanding of one of ordinary skill in the art, values that are sed as ranges can assume any specific value or sub—range within the stated ranges in different embodiments of the present disclosure, to the tenth of the unit of the lower limit of the range, unless the context clearly dictates otherwise.

This application refers to various issued patents, published patent applications, l articles, and other publications, all of which are incorporated herein by nce.

If there is a ct between any of the incorporated references and the t specification, the specification shall control. In on, any ular embodiment of the present disclosure that falls within the prior art may be explicitly ed from any one or more of the claims. Because such embodiments are deemed to be known to one of ordinary skill in the art, they may be excluded even if the exclusion is not set forth explicitly herein. Any particular embodiment of the t disclosure can be excluded from any claim, for any reason, whether or not related to the existence of prior art.

Those d in the art will ize or be able to ascertain using no more than routine experimentation many equivalents to the specific embodiments described herein.

The scope of the present embodiments described herein is not intended to be limited to the above Description, but rather is as set forth in the appended claims. Those of ordinary skill in the art will appreciate that various changes and modifications to this description may be made Without ing from the spirit or scope of the present disclosure, as defined in the following claims.

Claims (20)

What is claimed is:

1. A method for ing the endogenous level of contact system activation in a subject, the method comprising: (iv) collecting blood from a subject to an ted blood collection tube; (v) processing the blood to produce a plasma sample; and (vi) measuring the level of contact system activation in the plasma sample, wherein the evacuated blood collection tube ses a liquid formulation comprising a mixture of protease inhibitors, polybrene, and EDTA; wherein the mixture of protease inhibitors comprises benzamidine, soybean trypsin inhibitor, leupeptin, and 4-(2- aminoethyl) benzenesulfonyl fluoride hydrochloride ).

2. The method of claim 1, wherein the subject is a human subject that has been treated with a drug ing a component of the contact system.

3. The method of claim 2, wherein the component of the contact system is plasma kallikrein.

4. The method of claim 3, wherein the drug inhibits active plasma kallikrein.

5. The method of claim 4, wherein the drug is an antibody that binds active plasma rein.

6. The method of any one of claims 1-5, wherein step (iii) is performed by measuring the level of one or more biomarkers indicative of contact system activation.

7. The method of claim 6, wherein the one or more biomarkers are selected from the group consisting of prekallikrein, active plasma kallikrein (pKal), a2M-pKal x, active factor XII, active factor XI, high molecular weight kininogen (HMWK), and a bradykinin lite.

8. The method of claim 7, wherein the one or more biomarkers comprise cleaved HMWK and/or intact HMWK.

9. A method for assessing the level of a drug targeting the contact system in a subject, the method comprising: (iv) collecting blood from a subject to an evacuated blood collection tube; wherein the subject has been administered with a drug that s a component of the contact system; (v) processing the blood to produce a plasma ; and (vi) measuring the level of the drug in the plasma sample; wherein the evacuated blood collection tube comprises a liquid formulation comprising a mixture of protease inhibitors, polybrene, EDTA; wherein the mixture of protease inhibitors comprises benzamidine, soybean trypsin inhibitor, leupeptin, and 4-(2- aminoethyl) benzenesulfonyl fluoride hydrochloride (AEBSF).

10. The method of claim 9, wherein the drug inhibits active plasma kallikrein.

11. The method of claim 10, n the drug is an antibody that binds active plasma kallekrein.

12. A method for ing immunogenicity of a drug targeting the contact system, the method comprising: (iv) collecting blood from a subject to an evacuated blood collection tube; n the subject has been stered with a drug that s a component of the contact ; (v) processing the blood to produce a plasma sample; and (vi) measuring the level of antibodies that bind to the drug in the plasma sample; wherein the evacuated blood collection tube comprises a liquid formulation comprising a mixture of protease inhibitors, polybrene, EDTA; wherein the mixture of protease inhibitors comprises benzamidine, soybean trypsin inhibitor, leupeptin, and 4-(2- aminoethyl) benzenesulfonyl fluoride hydrochloride (AEBSF).

13. The method of claim 12, wherein the subject is a human t.

14. The method of claim 13, wherein the human subject is a human patient having a disease associated with the t system.

15. The method of claim 14, n the disease is hereditary angioedema (HAE).

16. The method of any one of claims 1-15, wherein the evacuated blood collection tube is a non-glass tube.

17. The method of claim 16, wherein the ted blood collection tube is a plastic tube.

18. The method of any one of claims 1-17, wherein in step (i), the evacuated blood collection tube is not the first tube filled with blood from the subject.

19. The method of any one of claims 1-18, wherein step (ii) is performed within one hour after step (i).

20. The method of any one of claims 1-19, wherein the liquid formulation ses 80-