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An Open-Label, Multi-Center Extension Study to Characterize the Long-Term Safety and Efficacy of BMS-986165 in Subjects with Moderate-to-Severe Plaque Psoriasis

Phase 1
Recruiting
Conditions
Moderate-to-Severe Plaque Psoriasis
MedDRA version: 20.0Level: LLTClassification code: 10071117Term: Plaque psoriasis Class: 10040785
Therapeutic area: Diseases [C] - Skin and Connective Tissue Diseases [C17]
Registration Number
CTIS2022-502361-15-00
Lead Sponsor
Bristol Myers Squibb International Corporation
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
1659
Inclusion Criteria

Completion of the protocol-required treatment period in an applicable study of BMS-986165 in moderate-to-severe psoriasis, Subjects must be willing to participate in IM011075 and must have the ability to sign the informed consent form (ICF), Women must not be pregnant, lactating, breastfeeding, or planning pregnancy during the study period(must have a negative urine test 24 hours prior to the start of study drug)

Exclusion Criteria

Any disease or medical condition that, in the opinion of the investigator, would make the subject unsuitable for this study, would interfere with the interpretation of subject safety or study results, or is considered unsuitable by the investigator for any other reason, Prior permanent discontinuation of study treatment in the parent study, Findings Related to Possible TB Infection, Evidence of active TB

Study & Design

Study Type
Interventional clinical trial of medicinal product
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Main Objective: To characterize the safety and tolerability of long-term use of BMS-986165 in subjects with moderate-to-severe plaque psoriasis;Secondary Objective: To characterize the maintenance of response to BMS-986165 in the treatment of subjects with moderate to severe plaque psoriasis;Primary end point(s): Adverse events and serious adverse events
Secondary Outcome Measures
NameTimeMethod
Secondary end point(s):sPGA 0/1 response;Secondary end point(s):PASI 75 response
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