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Open Label Study to Investigate the Safety and Efficacy of Ponesimod in Moderate-to-Severe Chronic Plaque Psoriasis

RecruitingPhase 3

A Multicenter, Open Label Study to Investigate the Safety and Efficacy of Ponesimod in the Treatment of Moderate-to-Severe Chronic Plaque Psoriasis

Who can join

Ages 18 to 65 · All sexes

Full eligibility criteria
Inclusion Criteria:

* Male and female subjects aged 18-65 years, inclusive
* BMI \>18 and \<40
* Minimum affected BSA of 10%
* PASI score ≥ 12
* PGA ≥ 3
* Diagnosed with moderate-to-severe plaque psoriasis

Exclusion Criteria:

* Diagnosis of generalized erythrodermic, generalized pustular (von Zumbusch), guttate, or palmoplantar psoriasis
* History of an allergic reaction or known and/or significant sensitivity to study drug

About the study

An open label study to investigate the safety and efficacy of ponesimod in participants with moderate-to-severe chronic plaque psoriasis

What is being tested

Sponsor: Vanda Pharmaceuticals · Participants: 300 · Started: Feb 17, 2026

Contact the study team

Official record on ClinicalTrials.gov — NCT07362017

Locations in the U.S.

ArizonaVanda Investigational Site, Glendale
CaliforniaVanda Investigational Site, Fremont
FloridaVanda Investigational Site, Miami
IndianaVanda Investigational Site, Indianapolis
New HampshireVanda Investigational Site, Portsmouth
New YorkVanda Investigational Site, Rochester
North CarolinaVanda Investigational Site, Wilmington
TexasVanda Investigational Site, San Antonio
Vanda Investigational Site, Webster
WashingtonVanda Investigational Site, Spokane

Conditions

From ClinicalTrials.gov, data retrieved Sep 30, 2026. Each study sets its own eligibility; the study team decides who can join.