DARTAccepted with a condition
No dedicated reproductive toxicology studies; tissue cross-reactivity study in human fetal/neonatal tissues requested postmarketing
Why: ICH S6(R1): generally not required for biologics to exogenous targets; no reproductive findings in monkey study or off-target binding · Within the guideline · Weight of evidence
“Dedicated reproductive toxicology studies have not been conducted with ansuvimab-zykl. In accordance with ICH S6(R1), reproductive toxicology studies are generally not required for biologics to exogenous targets.”
✓ VerifiedFDA integrated review, p. 89Source ↗ “In addition, no male or female reproductive toxicities were observed in the 4-week repeat-dose toxicology study in rhesus monkeys (Study #1016-1363), and no off-target binding was observed in the tissue cross-reactivity study in human tissues (Study #20101338). A tissue cross-reactivity study in human fetal and/or neonatal tissues will be requested in a postmarketing commitment (PMC).”
✓ VerifiedFDA integrated review, p. 89Source ↗ Efficacy modelAcceptedBeyond the letter
Nonhuman primate efficacy program, begun for the Animal Rule, was incomplete when the outbreak occurred
Why: Available NHP data sufficient for proof-of-concept and to support the single 50 mg/kg IV clinical dose · Serious disease
“When the 2018 Eastern DRC outbreak occurred, the nonclinical program was progressing but was incomplete. However, the NHP data were sufficient to support the proof-of-concept and use of a single 50 mg/kg IV dose of ansuvimab-zykl in the PALM Trial and expanded access program.”
✓ VerifiedFDA integrated review, p. 46Source ↗