At a glance
ClinicalIndex Comparison RecordStandardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.
A Phase 1, Single- Center, Randomized, Double-blind, Vehicle And Active Comparator-controlled Trial To Evaluate The Antipsoriatic Activity And Safety Of A Topically Applied Pf-06263276 Formulation In A Psoriasis Plaque Test
In Brief
A Phase 1 clinical trial evaluating PF06263276, Vehicle, and 3 other interventions for Psoriasis Vulgaris. Completed, enrolled 15 participants across 1 site.
Detailed Summary
This is a vehicle and comparator controlled Proof of Mechanism (PoM) trial to evaluate the effect on psoriasis disease activity and safety of topically applied PF 06263276 in subjects with psoriasis vulgaris.
Study Details
Timeline
Interventions
4% PF 06263276 solution Daily dosage: approximately 8 mg PF 06263276 QD
Active ingredient-free vehicle to 4% solution
Daily Dosage: approximately 4 mg tofacitinib
Active ingredient-free vehicle to 2% Ointment
Daivonex solution (50 ug/ml Calcipotriol) Daily Dosage of calcipotriol: approximately 0.01 mg
Daivonex ointment (50 ug/g Calcipotriol) Daily Dosage of calcipotriol: approximately 0.01 mg