| CPC G01N 33/6893 (2013.01) [C07K 16/36 (2013.01); C07K 16/40 (2013.01); C12Q 1/37 (2013.01); C12Q 1/56 (2013.01); A61K 2039/505 (2013.01); C07K 2317/76 (2013.01); C12Y 304/21034 (2013.01); C12Y 304/21038 (2013.01); G01N 2333/4713 (2013.01); G01N 2333/96455 (2013.01); G01N 2333/96458 (2013.01); G01N 2500/02 (2013.01); G01N 2500/20 (2013.01); G01N 2800/224 (2013.01); G01N 2800/50 (2013.01); G01N 2800/52 (2013.01)] | 9 Claims |

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1. A method for assessing plasma activation, comprising:
providing a plasma sample from a subject;
incubating the plasma sample with an activator of plasma kallikrein (pKal), wherein the activator is Factor XIIa (FXIIa) and wherein the activator is added ex vivo; and
measuring the level of cleaved high molecular weight kininogen (HMWK) in the plasma sample after ex vivo activation;
wherein the subject has been treated with a pKal inhibitor.
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