Monkey perivascular inflammation with ADA, CRP, IL-6, TNFa, IgG/IgM rises; complement Bb activation; ADA in some monkeys
“In the same study, five other animals across the three lowest dose groups showed perivascular mixed cell infiltration in multiple organs, associated with increases in anti-drug antibody, CRP, IL-6, MIP-1β, TNFα, and serum IgG and IgM”
✓ VerifiedFDA pharmacology/toxicology review, p. 14Source ↗
Biodistribution & persistence
Rapid plasma-to-tissue distribution; high levels in kidney, liver, lymph nodes, injection site, bone marrow
“High concentrations of inotersen were detected in kidneys, liver, mesenteric lymph nodes, injection site and bone marrow.”
Thrombocytopenia (monkey, clinically translated) and renal glomerular toxicity; PS-ASO class pro-inflammatory effects
“In the 39-week monkey study, severe thrombocytopenia associated with petechiae, bruising, and internal hemorrhages was observed within the first 11-14 weeks of dosing in two animals (one in each of the two highest dose groups), necessitating early euthanasia.”
✓ VerifiedFDA pharmacology/toxicology review, p. 14Source ↗
Anti-drug antibodies: animals
ADA in some monkeys of the 39-week study; median trough levels ~2- to 12-fold higher than ADA-negative animals
“However, anti-inotersen antibodies (ADAs) developed in some monkeys of the 39 weeks toxicity study, which increased the median plasma trough concentrations of inotersen at approximately 3 months or beyond from ~2- to 12-fold compared to those monkeys that did not develop antibodies (see section 3.2.3 below).”
Main pharmacology-related risk is increased susceptibility to infections (C5 inhibition); no complement activation by the aptamer in monkeys; panuveitis with Lucentis combination