Serum IL-12p40 rose only 2-fold at ~20x the human CpG 1018 dose; no IL-12p40 or IFN-gamma increase at the 1x human dose
“The 300 mcg 1018 ISS + HBsAg dose (approximately 20 times the human dose) induced only a 2-fold increase in IL-12p40 levels over baseline, and the 15 mcg 1018 ISS + HBsAg dose (a 1 X human dose) did not induce an increase in either IL-12p40 or IFN-g levels after the first or last injection.”
Rapid plasma decline; PS-ODN binds plasma proteins (95%) and distributes to kidney (up to 20% of dose), liver and spleen
“According to published data the rapid decline is due to initial low affinity binding to plasma proteins (95%) and to significant distribution to kidney (up to 20 % of the dose), liver, and to a minor extent spleen.”
Oligonucleotide class effect: CpG 1018 kidney accumulation in rats with non-reversible tubular degeneration and interstitial inflammation
“Most of the observed changes were reversible, except for accumulation of the CpG 1018 in the kidneys in male rats of all groups as well as female rats receiving 2.5 and 12.5 mg/kg/week which led to minimal to moderate tubular degeneration and minimal to moderate chronic interstitial inflammation in a dose dependent manner.”
✓ VerifiedFDA summary basis for approval, p. 15Source ↗
Anti-drug antibodies: animals
Not stated in public reviews
Not reported in the public reviews. Reviewers summarise selectively, so this usually means it wasn't discussed publicly, not that it wasn't studied.
Anti-drug antibodies: patients
Not stated in public reviews
Not reported in the public reviews. Reviewers summarise selectively, so this usually means it wasn't discussed publicly, not that it wasn't studied.
Main pharmacology-related risk is increased susceptibility to infections (C5 inhibition); no complement activation by the aptamer in monkeys; panuveitis with Lucentis combination