Low ADA incidence: rat negative, one monkey ADA-positive; no dedicated antigenicity studies
“All samples in the rat were negative. In the monkey study one sample was positive at 30 mg/kg/week (on day 169) and 3 samples were positive at 100 mg/kg/week, all from one animal (on days 85, 169 and 253).”
Rat QWBA: liver, kidney cortex, lymph nodes highest; long liver/kidney half-lives; persists in liver, kidney, injection site at 28 days
“Quantitative whole-body autoradiography confirmed that givosiran is distributed to a limited number of tissues, with high exposures observed in the liver, kidneys, kidney cortex, and lymph nodes.”
✓ VerifiedFDA multi-discipline review, p. 27Source ↗
“Tubular basophilic granules were observed in the kidney and may be related to accumulation of polyanionic oligonucleotide molecules in lysosomes.”
✓ VerifiedFDA multi-discipline review, p. 27Source ↗
Anti-drug antibodies: animals
Rat (26-week): all negative; monkey (39-week): ADA-positive samples at 30 and 100 mg/kg/week, mostly from one animal
“All samples in the rat were negative. In the monkey study one sample was positive at 30 mg/kg/week (on day 169) and 3 samples were positive at 100 mg/kg/week, all from one animal (on days 85, 169 and 253).”
Treatment-emergent ADA in 1/111 (0.9%) AHP patients
“In placebo-controlled and open-label clinical studies, 1 of 111 patients with AHP (0.9%) developed treatment-emergent anti-drug antibodies (ADA) during treatment with GIVLAARI.”
Main pharmacology-related risk is increased susceptibility to infections (C5 inhibition); no complement activation by the aptamer in monkeys; panuveitis with Lucentis combination