“Genetox and carcinogenicity studies were not conducted. The division waived the carcinogenicity study requirement after a review of the Sponsor’s Weight of Evidence justification (see review by Barbara Wilcox dated April 19, 2022).”
✓ VerifiedFDA integrated review (BLA 761463, original application, approved Sep 2026), p. 183Source ↗
Carcinogenicity
Not conducted; FDA waived the requirement after reviewing the sponsor's weight-of-evidence justification
“Genetox and carcinogenicity studies were not conducted. The division waived the carcinogenicity study requirement after a review of the Sponsor’s Weight of Evidence justification (see review by Barbara Wilcox dated April 19, 2022).”
✓ VerifiedFDA integrated review (BLA 761463, original application, approved Sep 2026), p. 183Source ↗
Reproductive & developmental
Rat fertility study: decreased sperm concentration, estrous disruption, reduced mating/fertility indices, increased postimplantation loss
“Reproductive and developmental toxicity: In the fertility and early embryonic development study in rat, decreased sperm concentration, estrous cycle disruption, decreased male and/or female mating and fertility indices, and increased postimplantation loss were observed.”
✓ VerifiedFDA integrated review (BLA 761463, original application, approved Sep 2026), p. 126Source ↗
Safety pharmacology
Incorporated into 4-week GLP monkey study (up to 100 mg/kg/week): no effects on respiration, neurological exams or ECG
“Safety pharmacology assessments were incorporated into the good laboratory practice (GLP) monkey toxicology study in which apitegromab (0, 10, 30, or 100 mg/kg/week) was administered weekly by IV bolus for 4 weeks. No apitegromab-related effects on respiration rate, neurological examinations, or ECGs were observed.”
✓ VerifiedFDA integrated review (BLA 761463, original application, approved Sep 2026), p. 181Source ↗
Genotox: Ames
Not conducted
“Genetox and carcinogenicity studies were not conducted. The division waived the carcinogenicity study requirement after a review of the Sponsor’s Weight of Evidence justification (see review by Barbara Wilcox dated April 19, 2022).”
“Genetox and carcinogenicity studies were not conducted. The division waived the carcinogenicity study requirement after a review of the Sponsor’s Weight of Evidence justification (see review by Barbara Wilcox dated April 19, 2022).”
“Genetox and carcinogenicity studies were not conducted. The division waived the carcinogenicity study requirement after a review of the Sponsor’s Weight of Evidence justification (see review by Barbara Wilcox dated April 19, 2022).”
Not conducted; FDA waived the requirement based on the sponsor's weight-of-evidence justification
“Genetox and carcinogenicity studies were not conducted. The division waived the carcinogenicity study requirement after a review of the Sponsor’s Weight of Evidence justification (see review by Barbara Wilcox dated April 19, 2022).”
Not required: carcinogenicity requirement waived by FDA on the sponsor's weight-of-evidence justification
“Genetox and carcinogenicity studies were not conducted. The division waived the carcinogenicity study requirement after a review of the Sponsor’s Weight of Evidence justification (see review by Barbara Wilcox dated April 19, 2022).”
No ECG, respiratory or neurological effects in 4-week GLP monkey study up to 100 mg/kg/week
“Safety pharmacology assessments were incorporated into the good laboratory practice (GLP) monkey toxicology study in which apitegromab (0, 10, 30, or 100 mg/kg/week) was administered weekly by IV bolus for 4 weeks. No apitegromab-related effects on respiration rate, neurological examinations, or ECGs were observed.”