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NCT05730725CompletedPhase 2

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

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

Source: ClinicalTrials.gov · Last updated 25 Nov 2025

Brief summary (registry, in English)

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

Status (registry)
Completed
Phase (registry)
Phase 2
Study type
Interventional
Enrollment
109 (actual)
First submitted
7 Feb 2023
Start date
3 Apr 2023
Primary completion date
6 Aug 2024
Lead sponsor
Bristol-Myers Squibb
Diseases
Psoriasis
NCT number
NCT05730725
EudraCT number
2023-504848-34

What you commit to

  • Study type: Interventional · Phase 2
  • Participants enrolled: 109
  • From 3 Apr 2023 to the primary completion date, 6 Aug 2024
  • 35 sites in 5 countries
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • 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

Other

  • Diagnosis of non-plaque psoriasis (guttate, inverse, pustular, erythrodermic)

Who the study is looking for

  • 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

Age in the registry: 18 years to 70 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (35)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
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BrisbaneAustraliaUnknown status
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CarltonAustraliaUnknown status
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Pascoe Vale SouthAustraliaUnknown status
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BarrieCanadaUnknown status
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HamiltonCanadaUnknown status
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LondonCanadaUnknown status
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St. John'sCanadaUnknown status
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TorontoCanadaUnknown status
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HinckleyUnited KingdomUnknown status
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LeytonstoneUnited KingdomUnknown status
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FukuokaJapanUnknown status
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NagoyaJapanUnknown status
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SapporoJapanUnknown status
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tabashi CityJapanUnknown status
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tabashi CityJapanUnknown status
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TsuJapanUnknown status
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BeverlyUnited StatesUnknown status
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BirminghamUnited StatesUnknown status
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ClarksvilleUnited StatesUnknown status
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ClevelandUnited StatesUnknown status
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Coral GablesUnited StatesUnknown status
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DallasUnited StatesUnknown status
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DurhamUnited StatesUnknown status
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EncinoUnited StatesUnknown status
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Fountain ValleyUnited StatesUnknown status
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FremontUnited StatesUnknown status
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LeawoodUnited StatesUnknown status
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Lee's SummitUnited StatesUnknown status
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Los AngelesUnited StatesUnknown status
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Los AngelesUnited StatesUnknown status
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PortsmouthUnited StatesUnknown status
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Rapid CityUnited StatesUnknown status
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Santa AnaUnited StatesUnknown status
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SkokieUnited StatesUnknown status
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WebsterUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.