Rat QWBA: highest in liver, lymph nodes, kidneys; detectable in all tissues at 672 h; not in fetal tissue
“Based on the QWBA data, radioactivity in tissues generally peaked by 48 hours postdose, and was highest in liver, lymph nodes, kidneys, and thoracic ducts.”
✓ VerifiedFDA pharmacology/toxicology review, p. 29Source ↗
Modality-specific risk
On-target vitamin A and thyroxine reduction (DART relevance); rat hepatocellular changes and renal basophilic granules
“vutrisiran was demonstrated to reduce circulating Vitamin A levels in monkey and human, consistent with TTR protein being a major carrier of Vitamin A.”
✓ VerifiedFDA pharmacology/toxicology review, p. 5Source ↗
Main pharmacology-related risk is increased susceptibility to infections (C5 inhibition); no complement activation by the aptamer in monkeys; panuveitis with Lucentis combination