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An Investigational Study to Evaluate Experimental Medication BMS-986165 Compared to Placebo in Participants With Plaque Psoriasis (POETYK-PSO-3) in Mainland China, Taiwan, and South Korea

Bristol-Myers Squibb (BMS) logo

Bristol-Myers Squibb (BMS)

Status and phase

Completed
Phase 3

Conditions

Psoriasis

Treatments

Drug: BMS-986165
Other: Placebo

Study type

Interventional

Funder types

Industry

Identifiers

NCT04167462
IM011-065

Details and patient eligibility

About

The purpose of this study is to investigate the experimental medication BMS-986165 compared to placebo in participants with moderate to severe plaque psoriasis in mainland China, Taiwan, and South Korea

Enrollment

220 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Plaque psoriasis for at least 6 months
  • Moderate to severe disease
  • Candidate for phototherapy or systemic therapy

Exclusion criteria

  • Other forms of psoriasis
  • History of recent infection
  • Prior exposure to BMS-986165

Other inclusion/exclusion criteria may apply.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Quadruple Blind

220 participants in 2 patient groups, including a placebo group

Arm A:BMS-986165 oral administration
Experimental group
Treatment:
Drug: BMS-986165
Arm B: Placebo oral administration
Placebo Comparator group
Treatment:
Other: Placebo

Trial documents
2

Trial contacts and locations

34

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Data sourced from clinicaltrials.gov

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