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
- Conditions
- Moderate-to-Severe Plaque PsoriasisMedDRA version: 20.0Level: LLTClassification code: 10071117Term: Plaque psoriasis Class: 10040785Therapeutic 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
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)
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
Name Time Method 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
Name Time Method Secondary end point(s):sPGA 0/1 response;Secondary end point(s):PASI 75 response