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An open label study to investigate the safety and efficacy of ponesimod in participants with moderate-to-severe chronic plaque psoriasis
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Ponesimod | Experimental | Ponesimod |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Ponesimod | Drug | Oral Tablet |
|
| Measure | Description | Time Frame |
|---|---|---|
| Safety and tolerability of ponesimod as measured by reporting of adverse events (AEs) | Safety will be assessed based on frequency of treatment-emergent adverse events and serious adverse events, and frequency of clinically notable abnormal vital signs, blood chemistry, hematology, urology, and ECGs | Through study completion, approximately 1 year |
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Inclusion Criteria:
Exclusion Criteria:
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| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Vanda Pharmaceuticals, Inc. | Contact | 202-734-3400 | clinicaltrials@vandapharma.com |
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| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Vanda Investigational Site | Recruiting | Glendale | Arizona | 85308 | United States | |
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| Vanda Investigational Site |
| Recruiting |
| Fremont |
| California |
| 94538 |
| United States |
| Vanda Investigational Site | Recruiting | Rochester | New York | 14623 | United States |
| Vanda Investigational Site | Recruiting | Spokane | Washington | 99202 | United States |
| ID | Term |
|---|---|
| D011565 | Psoriasis |
| ID | Term |
|---|---|
| D017444 | Skin Diseases, Papulosquamous |
| D012871 | Skin Diseases |
| D017437 | Skin and Connective Tissue Diseases |
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| ID | Term |
|---|---|
| C550169 | ponesimod |
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