SpeciesVerdict not stated
No pharmacologically relevant species or valid transgenic mouse; no repeat-dose toxicity studies; safety program mainly in vitro with human cells and tissues
Why: No species-specific cross-reactivity · No relevant species · Within the guideline
“Due to the lack of species-specific cross-reactivity, no relevant animal species or valid transgenic mouse models were identified in which to conduct the nonclinical toxicology studies.”
✓ VerifiedEMA assessment report, p. 16Source ↗ Safety pharmacologyAcceptedBeyond the letter
No safety pharmacology studies
Why: SLAMF7 binding not expected to affect CNS or cardiovascular function · Pharmacology or kinetics
“Binding to SLAMF7 by elotuzumab is therefore not expected to have effects on CNS parameters or cardiovascular functioning. The absence of specific safety pharmacology studies is therefore acceptable.”
✓ VerifiedEMA assessment report, p. 22Source ↗ DARTVerdict not stated
No reproductive and developmental toxicity studies; risk assessment based on SLAMF7 tissue distribution and published literature instead
Why: Lack of a pharmacologically relevant animal species · No relevant species · Weight of evidence
“Safety pharmacology, repeat dose toxicity, and reproductive and developmental toxicity studies were not conducted due to the lack of a pharmacologically-relevant animal species. The Applicant submitted a risk assessment for the potential for reproductive and developmental toxicity for elotuzumab based on the tissue distribution of SLAMF7 and published literature.”
✓ VerifiedFDA pharmacology/toxicology review, p. 12Source ↗