No effects on TDAR or immunophenotyping in juvenile rat; lymphoid necrosis in spleen/thymus at high dose in mouse
“No drug-related effects were observed on TDAR, immunophenotyping, physical development, neurobehavioral development, or on the male reproductive system.”
✓ VerifiedFDA pharmacology/toxicology review, p. 18Source ↗
Biodistribution & persistence
Rapid, widespread distribution; highest in kidney, low in brain; ~60% urinary excretion; only kidney retained at 56 days
“Widespread tissue distribution was detected by QWBA, with highest peak levels in kidney (165000 ng-eq/g). At 56 days postdose, radioactivity was detected only in kidney and urine.”
✓ VerifiedFDA pharmacology/toxicology review, p. 13Source ↗
Modality-specific risk
Renal tubular toxicity (PMO kidney accumulation); also lateral ventricle dilatation (mdx mouse) and juvenile bone density loss
“Regarding toxicity, the primary toxicities observed with eteplirsen were renal tubule degeneration/necrosis in all species tested (mdx mouse, juvenile rat, cynomolgus monkey), dilatation of lateral ventricles in mdx mouse, and decreases in bone mineral content and density in juvenile rat.”
✓ VerifiedFDA pharmacology/toxicology review, p. 20Source ↗
Main pharmacology-related risk is increased susceptibility to infections (C5 inhibition); no complement activation by the aptamer in monkeys; panuveitis with Lucentis combination