Last updated on November 2019

Efficacy and Safety of BMS-986165 Compared With Placebo in Participants With Active Psoriatic Arthritis (PsA)

Brief description of study

The main purpose of study is to assess the dose-response relationship of BMS-986165 (Dose A or Dose B once daily [QD]) at Week 16 in the treatment of participants with active PsA.

Detailed Study Description

The study is intended to evaluate the safety and efficacy of BMS-986165 Dose A or B once daily (QD) compared with placebo in adults with active PsA. The primary endpoint is american college of rheumatology (ACR) 20 response at Week 16 (Part A).

Clinical Study Identifier: NCT03881059

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CCR Ostrava

Ostrava, Czechia
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L.K.N. Arthrocentrum, s.r.o

Hlucin, Czechia
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