drugset / Trial / NCT04092452

A Study to Evaluate the Safety and Efficacy of PF-06650833, PF-06700841, and PF 06826647 in Adults With Hidradenitis Suppurativa

NCT04092452

Phase 2 Completed 194 enrolled Pfizer
RandomizedParallel-groupTriple-blindTreatment

Summary

This is a study with 3 kinase inhibitors (PF 06650833, PF 06700841 and PF 06826647) in participants with moderate to severe HS. The study will have a maximum duration of approximately 26 weeks. This includes an up to 6-week Screening Period, a 16 week Dosing Period and a 4 week Follow up Period.

Timeline

Start
2019-12-02
Primary completion
2022-01-10
Completion
2022-01-10

Drugs

EvaluationDrugModalityDoseRoute
Subject Brepocitinib Small molecule 45 mg
Subject ROPSACITINIB Small molecule 400 mg
Subject ZIMLOVISERTIB Small molecule 400 mg