Effect of Bimekizumab in Patients With Psoriasis Vulgaris and Active Psoriatic Arthritis
- Sponsor
- Innovaderm Research Inc.
- Study ID
- NCT05499416
- Phase
- PHASE4
- Status
- Withdrawn
Conditions
- Active Psoriatic Arthritis
- Psoriasis Vulgaris
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- Bimekizumab — DRUGSelf-administration of two (2-160 mg/mL \[1 mL\]) pre-filled syringes or autoinjectors at baseline (Day1) and at Weeks 4, 8,12, and 16
Study Details
This is an open-label study to evaluate the effects of bimekizumab in patients with psoriasis vulgaris and who also have active psoriatic arthritis (PsA).
Key Dates
- Start date
- Jan 31, 2023
- Status verified
- Mar 2023
- Primary completion
- Sep 30, 2023
- Completion
- Apr 30, 2024
Study Design
- Enrollment
- 0 participants (actual)
- Allocation
- NA
- Intervention model
- SINGLE_GROUP
- Primary purpose
- TREATMENT
Arms
- Experimental: Bimekizumab 320 mg SC injectionsBimekizumab 320 mg solution administered via SC injections every 4 weeks for 16 weeks.
Primary Outcome Measure
Physician Global Assessment (PGA) x Body Surface Area (BSA) [ Time Frame: Week 24 ]
Related Studies
- Psoriatic Immune Response to TildrakizumabPHASE4 · Recruiting · University of California, San Francisco · San Francisco, California
- Correction of Psoriatic T Cell Signatures by DeucravacitinibPHASE4 · Recruiting · University of California, San Francisco · San Francisco, California
- Efficacy and Safety of a Botanical Total Coumarin (TC) Cream in Treating Patients With Psoriasis Vulgaris (PLANTCOAT-III)PHASE3 · Recruiting · Psoriasis Research Institute of Guangzhou · New York, New York