Low immunogenicity: 1/128 (0.8%) SAPPHIRE patients ADA-positive at a single time point; no neutralizing antibodies
“In up to 52 weeks of treatment in SAPPHIRE, 1/128 (0.8%) of subjects treated with apitegromab tested positive for treatment-emergent anti-apitegromab antibodies (ADA) at a single time point. No neutralizing antibodies were detected.”
✓ VerifiedFDA integrated review (BLA 761463, original application, approved Sep 2026), p. 270Source ↗
Biodistribution & persistence
Rat single 10 mg/kg IV dose: Cmax 203 µg/mL, AUCinf 42936 µg*h/mL, half-life 222 hours
“In female rats, administration of a single IV dose of apitegromab (10 mg/kg) resulted in maximum plasma concentration (Cmax) and area under the concentration-time curve (AUC)inf values of 203 µg/mL and 42936 µg*h/mL, respectively and a half-life (t1/2) of 222 hours.”
✓ VerifiedFDA integrated review (BLA 761463, original application, approved Sep 2026), p. 181Source ↗
Modality-specific risk
Drug-related adverse bone effects in 12- and 26-week rat studies
“This and the previous findings in the 12-week study suggest an SRK-015-related effect on bone.”
✓ VerifiedFDA integrated review (BLA 761463, original application, approved Sep 2026), p. 183Source ↗
Anti-drug antibodies: animals
26-week rat: ADA in a few low-dose rats (dosing Days 43, 99; recovery Day 42); exposure apparently reduced in 2
“Anti-SRK-015 antibodies were detected during the dosing period in 1 LD male (Day 43) and 1 LD female (Day 99) and during the recovery period in 1 LD female (Day 42). TK data from the latter 2 animals were excluded from the analysis due to the apparent impact of ADA on serum drug concentrations.”
1/128 (0.8%) in SAPPHIRE (up to 52 weeks), at a single time point; no neutralizing antibodies
“In up to 52 weeks of treatment in SAPPHIRE, 1/128 (0.8%) of subjects treated with apitegromab tested positive for treatment-emergent anti-apitegromab antibodies (ADA) at a single time point. No neutralizing antibodies were detected.”
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