ADA in 9 of 36 treated monkeys (26-week study); ADA did not notably affect exposure
“Nine of 36 treated animals were positive for ADA post-dose (7/12 LD animals, 2/12 HD animals). Positive ADA response did not notably affect drug exposure.”
✓ VerifiedFDA multi-discipline review, p. 41Source ↗
“No plasma membrane staining with pozelimab was observed. Given the low likelihood that pozelimab will enter the cytoplasm of cells and in the absence of adverse effects in the 13- and 26-week toxicity studies, the risk of off-target binding by pozelimab resulting in clinically relevant toxicity is minimal.”
✓ VerifiedFDA multi-discipline review, p. 44Source ↗
Modality-specific risk
Serious infections, including meningococcal infections, from complement inhibition
“The increased risk of serious infections, including meningococcal infections associated with administration of pozelimab, will be included in the labeling as a Warning and Precaution.”
✓ VerifiedFDA multi-discipline review, p. 129Source ↗
Anti-drug antibodies: animals
Monkey ADA generally did not affect drug exposure or hasten elimination
“Positive ADA responses generally did not affect drug exposure or hasten elimination”
✓ VerifiedFDA multi-discipline review, p. 38Source ↗
Anti-drug antibodies: patients
None of 9 evaluable patients developed anti-pozelimab antibodies during 48 weeks
“Nine of the 10 patients 3 years of age and older with CD55-deficient PLE in the clinical study were evaluable for anti-pozelimab antibodies. None of these patients developed anti-pozelimab-bbfg antibodies during the 48-week treatment with pozelimab-bbfg.”
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