Open Label Study to Investigate the Safety and Efficacy of Ponesimod in Moderate-to-Severe Chronic Plaque Psoriasis
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
As published by the study on ClinicalTrials.gov. "Not stated" means the study hasn't said — ask the study team.
- Age
- 18 Years to 65 Years
- Sex
- All sexes
- Healthy volunteers
- Not accepted
- Compensation
- Not stated
Other requirements are listed under Eligibility below. Only the study team can confirm whether you can join.
What to expect
No one can promise a trial will help you personally — that is what the research is trying to find out.
What participation involves
Not stated in the study description — ask the study team about visits and procedures.
- Compensation
- Not stated
- Study-related exams and procedures are typically provided at no cost. This is how many trials work in general — confirm the details for this study with the study team.
- Participants are monitored closely by the research team throughout the study.
- Some participants may receive access to an investigational treatment, which is still being studied.
- Your participation helps researchers learn whether this approach could help future patients.
About this study
In plain language
This study tests how safe ponesimod is and how well it works for adults ages 18–65 with moderate-to-severe chronic plaque psoriasis. This is a long-lasting skin condition that causes thick, scaly patches. The study is open label, meaning participants and study staff know which drug is given.
An open label study to investigate the safety and efficacy of ponesimod in participants with moderate-to-severe chronic plaque psoriasis
Compensation is read from the study's own description and may be missing — always confirm with the study team.
Eligibility
Who can join
- Adults ages 18–65.
- Body mass index (BMI), a measure of weight compared with height, above 18 and below 40.
- Psoriasis covers at least 10% of the body’s skin.
- Psoriasis Area and Severity Index (PASI) score of at least 12, which measures how much skin is affected and how severe it is.
- Physician’s Global Assessment (PGA) score of at least 3, a doctor’s rating of psoriasis severity.
- Diagnosed with moderate-to-severe plaque psoriasis.
Who can't join
- Having certain other forms of psoriasis: widespread red skin (generalized erythrodermic), widespread pus-filled bumps (generalized pustular or von Zumbusch), small drop-shaped spots (guttate), or psoriasis on the palms or soles (palmoplantar).
- A past allergic reaction or known or major sensitivity to the study drug.
Simplified for readability. The official criteria below are what the study team uses.
Official 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
Study sites (10)
AZ
- Vanda Investigational Site · Glendale, AZ 85308More trials in Glendale
CA
- Vanda Investigational Site · Fremont, CA 94538More trials in Fremont
FL
- Vanda Investigational Site · Miami, FL 33126More trials in Miami
IN
- Vanda Investigational Site · Indianapolis, IN 46250More trials in Indianapolis
NC
- Vanda Investigational Site · Wilmington, NC 28405More trials in Wilmington
NH
- Vanda Investigational Site · Portsmouth, NH 03801More trials in Portsmouth
NY
- Vanda Investigational Site · Rochester, NY 14623More trials in Rochester
TX
- Vanda Investigational Site · San Antonio, TX 78213More trials in San Antonio
- Vanda Investigational Site · Webster, TX 77598More trials in Webster
WA
- Vanda Investigational Site · Spokane, WA 99202More trials in Spokane