No immunosuppression (TDAR) or T-cell depletion in monkey toxicity studies
“The immune function tests in the monkey toxicity studies showed that risankizumab did not cause immunosuppression [(as assessed by T-dependent antibody response (TDAR)] or deplete T-cells.”
✓ VerifiedFDA multi-discipline review, p. 55Source ↗
Biodistribution & persistence
Crosses placenta: infant serum exposure 25% and 17% of maternal on birth day 14 (5 and 50 mg/kg/week)
“The mean infant serum exposures were 25% and 17% of the mean maternal serum exposures on Birth Day (BD) 14 in the 5 and 50 mg/kg/week treatment groups, identifying the ability of risankizumab to cross the placenta.”
Embryo-fetal risk: treatment-related fetal/infant loss at 50 mg/kg/week in monkey ePPND
“Therefore, the increased fetal/infant loss in the 50 mg/kg/week group was considered to be related to risankizumab treatment.”
✓ VerifiedFDA multi-discipline review, p. 55Source ↗
Anti-drug antibodies: animals
26-week study: ADA in one of eight (5 mg/kg/week) and six of twelve (50 mg/kg/week) monkeys; exposure unaffected, no ADA-related safety events
“ADA positive results were observed in one of eight and six of twelve animals in the 5 and 50 mg/kg/week groups, respectively. Serum risankizumab concentrations were unaffected by ADAs and no ADA-dependent safety events were observed.”
Psoriasis: ~24% ADA by Week 52; ~57% of these neutralizing (14% of all subjects)
“By Week 52, approximately 24% (263/1079) of adults treated with SKYRIZI at the recommended dosage developed antibodies to risankizumab-rzaa. Of the subjects who developed antibodies to risankizumab-rzaa, approximately 57% (14% of all subjects treated with SKYRIZI) had antibodies that were classified as neutralizing.”
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