Low immunogenic potential (PBMC assay); no immunotoxicity in 13-week study; ADA assay drug interference
“Zanidatamab displayed low immunogenic potential in a functional human PBMC proliferation assay.”
✓ VerifiedFDA multi-discipline review, p. 40Source ↗
Biodistribution & persistence
No in vivo tissue distribution studies performed (mAb)
“In vivo tissue distribution studies have not been performed with zanidatamab.”
✓ VerifiedFDA multi-discipline review, p. 41Source ↗
Modality-specific risk
Embryo-fetal toxicity (HER2 class effect); diarrhea/GI findings in monkeys; no CRS signal
“On the basis of a weight-of-evidence analysis supported by published literature indicating that embryo-fetal toxicity is a likely class effect of HER2 binding antibodies”
✓ VerifiedFDA multi-discipline review, p. 46Source ↗
Anti-drug antibodies: animals
No confirmed ADA in monkeys, but drug levels exceeded assay drug tolerance; ADA may be undetected
“No zanidatamab-treated animals had detectable ADA in a confirmatory assay postdose, but the majority had serum concentrations of zanidatamab that exceeded the specific drug tolerance level of the confirmatory assay; thus, ADA may be present but undetectable due to high drug concentrations.”
✓ VerifiedFDA multi-discipline review, p. 40Source ↗
Anti-drug antibodies: patients
3.4% (18/534) treatment-emergent ADA; 17% (3/18) of these neutralizing
“In patients who received ZIIHERA at the approved recommended dosages, 3.4% (18/534) of patients developed treatment-emergent anti-zanidatamab antibodies. Of the patients who developed treatment-emergent anti-zanidatamab antibodies, 17% (3/18) also developed neutralizing antibodies.”