Low-titre ADA in 3/36 monkeys, no impact on exposure or tox; no ADA in rats; not immunostimulatory
“A low incidence, 3 out of 36 treated monkeys in the 36- week repeat-dose toxicity study (GO1-GLP15-036) were confirmed to have a low titre of anti-lumasiran antibodies.”
Rat: liver, kidney cortex/medulla highest; not detected in brain/spinal cord; long liver half-life (585 h) in monkey
“Relatively high tissue concentrations (in descending order) were observed in the liver, kidney cortex, kidney medulla, cecum, salivary gland, bone marrow, thyroid and pancreas.”
“AEs or toxicities associated with GalNAC-conjugated siRNA products include injection site reactions, ALT and AST elevations, mild increases in serum creatinine and decreases in eGFR, positive ADA, and hypersensitivity (including anaphylactic reactions).”
Low-titre ADA in 3/36 monkeys (36-week); no effect on exposure or toxicity; no ADA in rats
“A low incidence, 3 out of 36 treated monkeys in the 36- week repeat-dose toxicity study (GO1-GLP15-036) were confirmed to have a low titre of anti-lumasiran antibodies. Plasma exposure of lumasiran was not impacted and there were no toxicological findings attributed to the presence of ADAs in these animals. No ADAs were detected in treated rats.”
ADA in 7/120 (6%) lumasiran-treated individuals; no clinically significant impact
“Across all clinical studies in the lumasiran development program, including patients with PH1 and healthy volunteers dosed with OXLUMO, 7 of 120 (6%) lumasiran-treated individuals with mean follow-up duration of 8.9 months, tested positive for ADA, as early as from Day 29.”
Main pharmacology-related risk is increased susceptibility to infections (C5 inhibition); no complement activation by the aptamer in monkeys; panuveitis with Lucentis combination