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Completed Phase 2 Interventional Results available

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

ClinicalTrials.gov ID: NCT05730725

Public ClinicalTrials.gov record NCT05730725. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Jul 23, 2026, 8:56 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Multi-Center, Randomized, Double-Blind, Placebo-Controlled, Parallel Group Phase 2 Study to Evaluate the Clinical Efficacy and Safety of BMS-986322 in Participants With Moderate-to-Severe Psoriasis

Study identification

NCT ID
NCT05730725
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Bristol-Myers Squibb
Industry
Enrollment
109 participants

Conditions and interventions

Conditions

Interventions

  • BMS-986322 Drug
  • Placebo Other

Drug · Other

Eligibility (public fields only)

Age range
18 Years to 70 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Apr 2, 2023
Primary completion
Aug 5, 2024
Completion
Aug 5, 2024
Last update posted
Nov 24, 2025

2023 – 2024

United States locations

U.S. sites
19
U.S. states
13
U.S. cities
18
Facility City State ZIP Site status
Local Institution - 0006 Birmingham Alabama 35205-5021
Local Institution - 0012 Encino California 91436
Local Institution - 0005 Fountain Valley California 92708-3701
Local Institution - 0002 Fremont California 94538
Local Institution - 0001 Los Angeles California 90045-3606
Local Institution - 0016 Los Angeles California 90056
Local Institution - 0003 Santa Ana California 92701-2201
Local Institution - 0013 Coral Gables Florida 33134-5736
Local Institution - 0056 Skokie Illinois 60077-1049
Local Institution - 0044 Clarksville Indiana 47129-2201
Local Institution - 0057 Leawood Kansas 66211
Local Institution - 0004 Beverly Massachusetts 01915-1672
Local Institution - 0060 Lee's Summit Missouri 64064
Local Institution - 0007 Portsmouth New Hampshire 03801
Local Institution - 0055 Durham North Carolina 27713-8507
Local Institution - 0008 Cleveland Ohio 44106-1716
Local Institution - 0058 Rapid City South Dakota 57702-9208
Local Institution - 0059 Dallas Texas 75230-5808
Local Institution - 0011 Webster Texas 77598

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 16 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT05730725, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Nov 24, 2025 · Synced Jul 23, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete protocol, eligibility criteria, and contact information for NCT05730725 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →