Psoriasis Clinical Trial

A Study to Evaluate Effectiveness and Safety of BMS-986322 in Participants With Moderate-to-Severe Psoriasis

Summary

The purpose of this study is to evaluate clinical effectiveness and safety of BMS-986322 in participants with moderate-to-severe psoriasis.

View Eligibility Criteria

Eligibility Criteria

Inclusion Criteria:

Diagnosis of plaque psoriasis (PsO) for ≥ 6 months
Body mass index 18 to 40 kg/m^2 and total body weight > 50 kg (110 lbs)
Deemed by Investigator to be eligible for phototherapy or systemic therapy
Psoriatic plaques must cover ≥ 10% of body surface area at baseline
Psoriasis Area and Severity Index (PASI) score ≥ 12 and static Physician Global Assessment (sPGA) ≥ 3 at baseline

Exclusion Criteria:

Diagnosis of non-plaque psoriasis (guttate, inverse, pustular, erythrodermic)
Diagnosis of uveitis, inflammatory bowel disease, or other immune-mediated conditions that are commonly associated with PsO for which a participant requires current systemic immunosuppressant medical treatment
Any significant acute or chronic medical illness

Other protocol-defined inclusion/exclusion criteria apply

Study is for people with:

Psoriasis

Phase:

Phase 2

Estimated Enrollment:

120

Study ID:

NCT05730725

Recruitment Status:

Active, not recruiting

Sponsor:

Bristol-Myers Squibb

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There are 35 Locations for this study

See Locations Near You

Local Institution - 0006
Birmingham Alabama, 35205, United States
Local Institution - 0012
Encino California, 91436, United States
Local Institution - 0005
Fountain Valley California, 92708, United States
Local Institution - 0002
Fremont California, 94538, United States
Local Institution - 0001
Los Angeles California, 90045, United States
Local Institution - 0016
Los Angeles California, 90056, United States
Local Institution - 0003
Santa Ana California, 92701, United States
Local Institution - 0013
Coral Gables Florida, 33134, United States
Local Institution - 0056
Skokie Illinois, 60077, United States
Local Institution - 0044
Clarksville Indiana, 47129, United States
Local Institution - 0057
Leawood Kansas, 66211, United States
Local Institution - 0004
Beverly Massachusetts, 01915, United States
Local Institution - 0060
Lee's Summit Missouri, 64064, United States
Local Institution - 0007
Portsmouth New Hampshire, 03801, United States
Local Institution - 0055
Durham North Carolina, 27713, United States
Local Institution - 0008
Cleveland Ohio, 44106, United States
Local Institution - 0058
Rapid City South Dakota, 57702, United States
Local Institution - 0059
Dallas Texas, 75230, United States
Local Institution - 0011
Webster Texas, 77598, United States
Local Institution - 0024
Brisbane Queensland, 4102, Australia
Local Institution - 0019
Carlton Victoria, 3053, Australia
Local Institution - 0045
Pascoe Vale South Victoria, 3044, Australia
Local Institution - 0062
St. John's Newfoundland and Labrador, A1E 1, Canada
Local Institution - 0034
Barrie Ontario, L4M 7, Canada
Local Institution - 0020
Hamilton Ontario, L8L 3, Canada
Local Institution - 0041
London Ontario, N6A 2, Canada
Local Institution - 0030
Toronto Ontario, M2N 3, Canada
Local Institution - 0049
Sapporo-Shi Hokkaido, 064-0, Japan
Local Institution - 0023
Itabashi Tokyo, 17386, Japan
Local Institution - 0051
Fukuoka-shi , 814-0, Japan
Local Institution - 0042
Itabashi-Ku , 173-8, Japan
Local Institution - 0026
Nagoya-Shi , 467-8, Japan
Local Institution - 0027
Tsu City , 514-8, Japan
Local Institution - 0050
Hinckley LEC, LE10 , United Kingdom
Local Institution - 0046
Leytonstone , E11 1, United Kingdom

How clear is this clinincal trial information?

Study is for people with:

Psoriasis

Phase:

Phase 2

Estimated Enrollment:

120

Study ID:

NCT05730725

Recruitment Status:

Active, not recruiting

Sponsor:


Bristol-Myers Squibb

How clear is this clinincal trial information?

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