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 — DRUG
    Oral 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: Ponesimod
    Ponesimod

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

Locations (4)

FacilityCityStateZIPSite coordinators
Vanda Investigational SiteGlendaleArizona85308-
Vanda Investigational SiteFremontCalifornia94538-
Vanda Investigational SiteRochesterNew York14623-
Vanda Investigational SiteSpokaneWashington99202-

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