Open Label Study to Investigate the Safety and Efficacy of Ponesimod in Moderate-to-Severe Chronic Plaque Psoriasis
Part of paid clinical trials in Glendale, Arizona.
- Sponsor
- Vanda Pharmaceuticals
- Study ID
- NCT07362017
- Phase
- PHASE3
- Status
- Recruiting
Conditions
- Moderate-to-severe Chronic Plaque Psoriasis
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - 65 Years
- Healthy Volunteers
- Not accepted
Interventions
- Ponesimod — DRUGOral Tablet
Study Details
An open label study to investigate the safety and efficacy of ponesimod in participants with moderate-to-severe chronic plaque psoriasis
Key Dates
- Start date
- Feb 17, 2026
- Status verified
- Jun 2026
- Primary completion
- Aug 31, 2028
- Completion
- Dec 31, 2028
Study Design
- Enrollment
- 300 participants (estimated)
- Allocation
- NA
- Intervention model
- SINGLE_GROUP
- Primary purpose
- TREATMENT
Arms
- Experimental: PonesimodPonesimod
Primary Outcome Measure
Safety and tolerability of ponesimod as measured by reporting of adverse events (AEs) [ Time Frame: Through study completion, approximately 1 year ]
Central Contacts
- Vanda Pharmaceuticals, Inc.202-734-3400
Locations (4)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| Vanda Investigational Site | Glendale | Arizona | 85308 | - |
| Vanda Investigational Site | Fremont | California | 94538 | - |
| Vanda Investigational Site | Rochester | New York | 14623 | - |
| Vanda Investigational Site | Spokane | Washington | 99202 | - |