ADA induced in all monkey repeat-dose studies, causing loss of exposure without affecting study interpretation
“Concizumab induced ADA in all repeat dose toxicity studies. ADA led to loss in exposure although this did not affect the overall interpretation of the studies.”
TCR: binding to TFPI-expressing tissues; cytoplasmic off-target binding unlikely to be relevant in vivo
“In a tissue cross reactivity study, concizumab showed anticipated binding to tissue in which TFPI is expressed. Off target binding was observed for cytoplasm but it is very unlikely that concizumab will be able to reach the cytoplasm in vivo.”
Thrombosis from exaggerated procoagulant pharmacology: thrombi at ≥10 (13-week), ≥3 (26-week) and ≥1 mg/kg/day (52-week) SC
“Pharmacology mediated formation of thrombi manifested in cynomolgus monkeys dosed subcutaneously during toxicology studies of 13-weeks (≥ 10 mg/kg/day), 26-weeks (≥ 3 mg/kg/day) and 52-weeks (≥ 1 mg/kg/day) in duration”
ADAs in cynomolgus monkeys correlated with reduced exposure and pharmacodynamic activity; considered inhibitory (particularly at low dose)
“When ADAs were detected, their presence correlated with a decline in pharmacodynamic activity (e.g., fibrinogen, TAT, and D-dimers) and a reduction in systemic exposure, indicating that the ADAs produced in cynomolgus monkeys (particularly at the LD) were inhibitory in nature.”
22.2% (71/320) developed ADA; 25.4% of ADA-positive had neutralizing antibodies
“71 out of the 320 treated patients (22.2%) developed anticoncizumab-mtci antibodies. Among the 71 patients who tested positive for ADA, 18 patients (25.4%) developed neutralizing antibodies (NAbs) against concizumab-mtci.”
In vitro whole-blood cytokine release far below alemtuzumab/TGN1412 controls; no effects on monkey TDAR, lymphocyte subsets or serum cytokines; ADA in some monkeys