CarcinogenicityAcceptedBeyond the letter
No rodent carcinogenicity study; carcinogenic risk assessed by weight of evidence including murine tumour surveillance studies with surrogate
Why: Data with siltuximab and other IL-6 inhibitors suggest low carcinogenic potential; weight of evidence does not indicate a human risk · Weight of evidence · Class precedent
“Rodent carcinogenicity studies have not been conducted with siltuximab. Evidence from studies conducted with siltuximab and other IL-6 inhibitors suggest that the potential for siltuximab to cause carcinogenicity is low.”
✓ VerifiedEMA assessment report, p. 29Source ↗ “The relevance of the findings to humans is undetermined but the weight of evidence approach used to determine the carcinogenic risk of siltuximab does not indicate a risk for humans.”
✓ VerifiedEMA assessment report, p. 26Source ↗ DARTAcceptedBeyond the letter
Fertility tested in mice with a rat anti-mouse IL-6 surrogate; ePPND in monkeys with a humanized siltuximab variant
Why: Binding, inhibition and epitope mapping showed the surrogates were suitable surrogates for siltuximab · Pharmacology or kinetics
“A fertility study was conducted with a rat anti-mouse IL6 mAb (CNTO 345) in mice and an enhanced pre- and post-natal development (ePPND) study was conducted with a humanized version of siltuximab (CNTO 136) in cynomolgus monkeys.”
✓ VerifiedFDA pharmacology/toxicology review, p. 16Source ↗ “Studies determining the binding, inhibition, and epitope mapping were performed demonstrating the suitability of CNTO 345 and CNTO 136 for their use as surrogates of siltuximab in toxicology studies.”
✓ VerifiedFDA pharmacology/toxicology review, p. 16Source ↗