At a glance
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A Randomized, Double-Blind, Placebo-Controlled, 12-week Dose-Ranging Trial of IMO-8400 in Patients With Moderate to Sever Plaque Psoriasis
In Brief
A Phase 2 clinical trial evaluating IMO-8400 Regimen 1, IMO-8400 Regimen 2, and 3 other interventions for Plaque Psoriasis. Completed, enrolled 46 participants across 1 site.
Detailed Summary
IMO 8400 is a second-generation oligonucleotide antagonist of endosomal Toll-like receptors (TLR) 7, TLR8 and TLR9. These TLR react to complexes of exogenous nucleic acids (as might be encountered during infection) and endogenous nucleic acids (as might be released during tissue damage during autoimmune disease). In vitro and in multiple animal models of autoimmune disease, IMO-8400 blocks immune activation mediated through TLR7, 8 and 9. In Phase 1 studies (Protocol 8400-001) IMO 8400 has been administered to healthy adults by SC injection at single-doses and multiple-doses (4 weeks) up to 0.6 mg/kg. All treatments were well-tolerated, with mild injection site reactions and no pattern of systemic reactions or laboratory changes. The current study represents the first clinical trial of IMO-8400 in patients with active autoimmune disease. Moderate to severe plaque psoriasis was chosen for this 12-week proof of activity trial based on a prior 4-week study using a first generation TLR7 and 9 antagonist which demonstrated clinical improvement in this patient population.
Study Details
Timeline
Interventions
IMO-8400 0.075 mg/kg q wk x 12 wk by subcutaneous injection
IMO-8400 0.15 mg/kg q wk x 12 wk by subcutaneous injection
IMO-8400 0.3 mg/kg q wk x 12 wk by subcutaneous injection
Saline q wk x 12 wk by subcutaneous injection
IMO-8400 0.6 mg/kg q wk x 12 wk by subcutaneous injection