Status:
COMPLETED
A Study to Evaluate the Efficacy and Safety of Bimekizumab in Chinese Adult Study Participants With Moderate to Severe Plaque Psoriasis
Lead Sponsor:
UCB Biopharma SRL
Conditions:
Chronic Plaque Psoriasis
Moderate to Severe Chronic Plaque Psoriasis
Eligibility:
All Genders
18+ years
Phase:
PHASE3
Brief Summary
The primary purpose of this study is to compare the efficacy of bimekizumab administered subcutaneously (sc) for 16 weeks versus placebo in the treatment of study participants with moderate to severe ...
Eligibility Criteria
Inclusion
- Study participant is Chinese male or female ≥18 years of age
- Study participant has plaque psoriasis (PSO) for ≥6 months prior to the Screening Visit
- Study participant has Psoriasis Area and Severity Index (PASI) ≥12 and body surface area (BSA) affected by PSO ≥10% and Investigator's Global Assessment (IGA) score ≥3 on a 5-point scale.
- Study participant is a candidate for systemic PSO therapy and/or phototherapy
- Female study participants must be postmenopausal or permanently sterilized or if childbearing potential must be willing to use protocol defined highly effective method of contraception throughout the duration of the study until 17 weeks after last administration of investigational medicinal product (IMP) and have a negative pregnancy test at Screening and prior to first dose
Exclusion
- Female study participant who is breastfeeding, pregnant, or plans to become pregnant during the study or within 17 weeks following the final dose of IMP
- Study participant has a form of PSO other than chronic plaque-type (eg, pustular, erythrodermic, guttate, or drug-induced PSO)
- Study participant has an active infection or history of infection(s) as defined in the protocol
- Study participant has known tuberculosis (TB) infection, is at high risk of acquiring TB infection, or has current or history of nontuberculous mycobacterium (NTMB) infection.Study participant has a past history of active TB involving any organ system unless adequately treated and is proven to be fully recovered upon consult with a TB specialist
- Study participant has a diagnosis of inflammatory conditions other than PSO vulgaris or psoriatic arthritis (PsA)
- Study participant has presence of significant uncontrolled neuropsychiatric disorder. Study participants with history of suicide attempt within the 5 years prior to the Screening Visit must be excluded. Study participants with history of suicide attempt more than 5 years prior to the Screening Visit must be evaluated by a mental health care practitioner before enrollment.
Key Trial Info
Start Date :
October 31 2023
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
February 5 2025
Estimated Enrollment :
133 Patients enrolled
Trial Details
Trial ID
NCT06011733
Start Date
October 31 2023
End Date
February 5 2025
Last Update
March 10 2025
Active Locations (18)
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1
Ps0041 20023
Beijing, China
2
Ps0041 20247
Beijing, China
3
Ps0041 20306
Beijing, China
4
Ps0041 20117
Guangzhou, China