“resulted in increased incidence and/or severity of meningeal and/or cerebral vascular inflammation, thrombosis, and/or hemorrhage at the mid and high doses consistent with slight exacerbation of the cerebral amyloid angiopathy that increases with aging in this mouse model.”
✓ VerifiedFDA pharmacology/toxicology review, p. 7Source ↗
Anti-drug antibodies: animals
Tg2576 mice: few ADA-positive animals with ~65% lower exposure; impact on study negligible
“Similarly, the two HD ADA-positive ch12F6A-dosed animals showed reductions of ~65% in plasma h12F6A exposure. Based on the small number of animals affected, the impact of ATA on the results of the study was negligible.”
✓ VerifiedFDA pharmacology/toxicology review, p. 33Source ↗
Anti-drug antibodies: patients
Up to 0.6% (15/2689) developed anti-aducanumab antibodies over up to 41 months; neutralizing not assessed
“In up to 41 months of treatment in the combined placebo-controlled and long-term extension periods of Studies 1 and 2, up to 0.6% (15/2689) of patients receiving ADUHELM once monthly developed anti-aducanumab-avwa antibodies.”
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