Embryo-fetal toxicity from IGF signalling inhibition (fetal growth restriction, teratogenicity); impaired growth and bone in juveniles
“The developmental adverse effects observed are consistent with the pharmacology of teprotumumab as an inhibitor of IGF signalling pathways which are known to be involved in regulation of fetal growth and development.”
In vitro whole-blood cytokine release far below alemtuzumab/TGN1412 controls; no effects on monkey TDAR, lymphocyte subsets or serum cytokines; ADA in some monkeys