Delayed/suppressed TDAR (KLH IgM/IgG) in 40-week monkey study, reversible; sporadic low-titre ADA without PD impact
“In a 40-week toxicity study in NHPs, delayed or suppressed IgM (data not shown) and IgG (see Figure 1, below) responses were observed across the dose range at ≥ 2 times the clinical MRHD (BSA) (≥ 30 mg/kg Q4W) in response to keyhole limpet hemocyanin (KLH) sheep antigen”
✓ VerifiedFDA pharmacology/toxicology review, p. 5Source ↗
“In rats, inclisiran-associated radioactivity widely distributed to most tissues with the highest concentrations (based on Cmax) observed at the subcutaneous dose site, and in the liver (target organ), and kidney cortex (site of elimination).”
✓ VerifiedFDA pharmacology/toxicology review, p. 26Source ↗
“Toxicities with inclisiran were generally non-adverse and largely secondary to tissue accumulation of drug.”
✓ VerifiedFDA pharmacology/toxicology review, p. 5Source ↗
Anti-drug antibodies: animals
Sporadic low-titre ADA in monkeys near end of dosing: 5 animals (15-week) and 3 (40-week)
“In the 15 and 40-week toxicology studies conducted in monkeys there were sporadic incidences of animals developing ADA at or near the end of the dosing periods. Five animals in the 15-week study and three animals in the 40 week study developed low titre ADA.”
Treatment-emergent ADA in 90/1,830 (5%) adults over 18 months; 33/1,830 (2%) positive before treatment
“Confirmed positivity was detected in 33/1,830 (2%) patients prior to receiving LEQVIO and in 90/1,830 (5%) patients during the 18 months of treatment with LEQVIO.”
Main pharmacology-related risk is increased susceptibility to infections (C5 inhibition); no complement activation by the aptamer in monkeys; panuveitis with Lucentis combination