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NCT01093326 · ClinicalTrials.gov registry record · Phase 2

Clinical Study to Investigate the Long-term Safety, Tolerability, and Efficacy of Ponesimod in Patients With Relapsing-remitting Multiple Sclerosis

A Phase 2 study, sponsored by Actelion.

Completed
Registry status
Phase 2
Development phase
353
Enrollment target

NCT01093326: Completed Phase 2 study, sponsored by Actelion.

NCT01093326 is a Phase 2 study that has completed, run by Actelion. The registered enrollment target is 353 participants, above the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (165% higher). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT01093326, a Phase 2 study, has completed, sponsored by Actelion.

COMPLETED
Registry status
Phase 2
Development phase
353 participants
Enrollment target

Study Summary

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.

Primary Outcome

ARR is defined as the number of confirmed relapses per year. A relapse is defined as the occurrence of an acute episode of one or more new symptoms, or worsening of existing symptoms of multiple sclerosis (MS), not associated with fever or infection, and lasting for at least 24 hours after a stable period of at least 30 days. A confirmed relapse is a relapse accompanied by an increase from the previous clinically stable assessment (that is, performed at least 30 days after the onset of any previ

Interventions

  • DRUG Ponesimod 10 mg
  • DRUG Ponesimod 20 mg
  • DRUG Ponesimod 40 mg

Trial Details

FieldValue
Enrollment Target 353 participants
Start Date 2010-05-12
Est. Completion 2023-09-06
Phase Phase 2
Actelion

63 total trials

What the finished NCT01093326 record still lists

NCT01093326 is an interventional study that assigns participants to a tested intervention. The registered 353 participants enrollment target is mid-sized for trials with a published cap, above the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (165% higher).

The record links to 0 conditions, and to 3 interventions - of which Ponesimod 10 mg is the first listed.

NCT01093326 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01093326 about?

NCT01093326 is a clinical study titled "Clinical Study to Investigate the Long-term Safety, Tolerability, and Efficacy of Ponesimod in Patients With Relapsing-remitting Multiple Sclerosis". 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.

What is the current status of trial NCT01093326?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 353 participants. The study started on 2010-05-12. Estimated completion is 2023-09-06.

What interventions are being tested in trial NCT01093326?

The interventions under investigation include: Ponesimod 10 mg (DRUG), Ponesimod 20 mg (DRUG), Ponesimod 40 mg (DRUG).

Who is sponsoring clinical trial NCT01093326?

This trial is sponsored by Actelion, which has 63 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT01093326's enrollment target sits among peer trials

353 129th of 2000 higher than 1,871 of 2,000 other Phase 2 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 2 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT01093326, the US trial registry maintained by the National Library of Medicine. NCT01093326 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.