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Last Updated: May 13, 2021

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CLINICAL TRIALS PROFILE FOR PONESIMOD

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All Clinical Trials for Ponesimod

Trial ID Title Status Sponsor Phase Start Date Summary
NCT01093326 Clinical Study to Investigate the Long-term Safety, Tolerability, and Efficacy of Ponesimod in Patients With Relapsing-remitting Multiple Sclerosis Active, not recruiting Actelion Phase 2 2010-05-01 This study is an extension to the study AC-058B201 and will investigate the long-term safety, tolerability and efficacy of ponesimod in patients with relapsing-remitting multiple sclerosis.
NCT02068235 Study to Investigate the Absolute Bioavailability of a Single Oral Dose of Ponesimod in Healthy Male Subjects Completed Actelion Phase 1 2014-08-01 This study consists of a single-dose pilot phase and a randomized, two-way crossover, single-dose main phase.The aim of this study is to evaluate the absolute bioavailability of the oral formulation (tablet) of ponesimod compared to an intravenous (i.v.) ponesimod formulation. Three subjects will be included in the pilot phase and 12 subjects in the main crossover phase.
NCT02136888 Study of the Electrocardiographic Effects of Ponesimod in Healthy Male and Female Subjects Completed Actelion Phase 1 2011-08-01 The aim of this study is to demonstrate that therapeutic and supratherapeutic plasma exposures to ponesimod do not have an effect on cardiac repolarization exceeding the threshold of regulatory concern as measured by the QTc (interval from beginning of the Q wave until end of the T wave corrected for heart rate) interval duration after administration of multiple oral doses of 40 mg and 100 mg to healthy male and female subjects.
NCT02425644 Oral Ponesimod Versus Teriflunomide In Relapsing MUltiple Sclerosis Recruiting Actelion Phase 3 2015-04-01 International clinical trial to compare ponesimod and teriflunomide in relapsing multiple sclerosis
NCT02461134 Clinical Study to Investigate the Biological Activity, Safety, Tolerability, and Pharmacokinetics of Ponesimod in Subjects With Symptomatic Chronic GVHD Active, not recruiting Actelion Phase 2 2016-02-01 Chronic graft versus host diseasre (GVHD) is a serious reaction that might occur in a person (the host) who has received cells or organs (graft) from another person because the graft attacks the host's cells. Currently there are no approved therapies for chronic GVHD in the USA, and patients with chroninc GVHD are treated with immunosuppressant drugs. T-lymphocytes (a type of white blood cells) are likely to play a role in the development of chronic GVHD. Due to the capacity of ponesimod to block the traffic of T-lymphocytes, ponesimod may be a new therapeutic approach to treat chroninc GVHD. The main objective of this study is to assess the effectiveness and safety of several doses of ponesimod in subjects with chronic GVHD who did not respond to standard available treatments.
>Trial ID >Title >Status >Phase >Start Date >Summary

Clinical Trial Conditions for Ponesimod

Condition Name

Condition Name for Ponesimod
Intervention Trials
Multiple Sclerosis 4
Healthy 3
Chronic Graft Versus Host Disease 1
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Condition MeSH

Condition MeSH for Ponesimod
Intervention Trials
Sclerosis 4
Multiple Sclerosis 4
Graft vs Host Disease 1
Multiple Sclerosis, Relapsing-Remitting 1
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Clinical Trial Locations for Ponesimod

Trials by Country

Trials by Country for Ponesimod
Location Trials
United States 39
Canada 7
Russian Federation 3
United Kingdom 3
Israel 2
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Trials by US State

Trials by US State for Ponesimod
Location Trials
Indiana 4
New York 3
Florida 3
California 3
Washington 3
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Clinical Trial Progress for Ponesimod

Clinical Trial Phase

Clinical Trial Phase for Ponesimod
Clinical Trial Phase Trials
Phase 3 3
Phase 2 2
Phase 1 3
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Clinical Trial Status

Clinical Trial Status for Ponesimod
Clinical Trial Phase Trials
Completed 2
Not yet recruiting 2
Active, not recruiting 2
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Clinical Trial Sponsors for Ponesimod

Sponsor Name

Sponsor Name for Ponesimod
Sponsor Trials
Actelion 7
Janssen Pharmaceutica N.V., Belgium 1
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Sponsor Type

Sponsor Type for Ponesimod
Sponsor Trials
Industry 8
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