No anti-dabigatran antibodies; circulating immune complexes normal; no renal immune complex deposition in monkeys
“However, there was no evidence for the development of anti-dabigatran antibodies. Circulating immune complexes were within normal limits in all animals and there was no evidence for immune complex deposition in the kidneys as evaluated by immunohistochemistry.”
Half-life about 6 h in rats and 4-5 h in rhesus monkeys; low clearance and small volume of distribution
“The plasma concentration-time profile was biphasic with a rapid initial decline phase and a slow terminal phase, with a half-life of approx. 6 hrs in rats and 4-5 hrs in rhesus monkeys. The clearance of idarucizumab was low and the volume of distribution was small.”
Potential prothrombotic activity investigated (D-dimer, F1+2); no prothrombotic effect found
“Apart from general toxicity, the 2-week study in rhesus monkeys also investigated the potential for pro-thrombotic activity of idarucizumab. Based on D-dimer and F1+2 evaluation, there was no evidence for a pro-thrombotic effect of idarucizumab.”
Anti-idarucizumab antibodies in some monkeys (end of treatment and recovery); no anti-dabigatran antibodies; circulating immune complexes normal
“In this study anti-idarucizumab antibodies were detected in some of the animals at the end of treatment and also at the end of the recovery period. However, there was no evidence for the development of anti-dabigatran antibodies. Circulating immune complexes were within normal limits in all animals”
Treatment-emergent low-titre ADA in 4% (10/224) of subjects and 2% (8/501) of patients
“Treatment-emergent possibly persisting anti-idarucizumab antibodies with low titers were observed in 4% (10/224) of the subjects and 2% (8/501) of patients treated with idarucizumab.”
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