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Completed Phase 2 Interventional Results available

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

ClinicalTrials.gov ID: NCT01093326

Public ClinicalTrials.gov record NCT01093326. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 19, 2026, 12:03 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

Multicenter, Randomized, Double-blind, Parallel-group Extension to Study AC-058B201 to Investigate the Long-term Safety, Tolerability, and Efficacy of Three Doses of Ponesimod, an Oral S1P1 Receptor Agonist, in Patients With Relapsing-remitting Multiple Sclerosis

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

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.

Study identification

NCT ID
NCT01093326
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Actelion
Industry
Enrollment
353 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years to 55 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
May 12, 2010 (Actual)
Primary completion
Sep 6, 2023 (Actual)
Completion
Sep 6, 2023 (Actual)
Last update posted
Mar 30, 2025

2010 – 2023

United States locations

U.S. sites
16
U.S. states
10
U.S. cities
16
Facility City State ZIP Site status
Not listed Phoenix Arizona — —
Not listed Scottsdale Arizona — —
Not listed Palo Alto California — —
Not listed Sacramento California — —
Not listed Venice Florida — —
Not listed Indianapolis Indiana — —
Not listed Kansas City Kansas — —
Not listed Lenexa Kansas — —
Not listed Latham New York — —
Not listed Schenectady New York — —
Not listed Stony Brook New York — —
Not listed Raleigh North Carolina — —
Not listed Cincinnati Ohio — —
Not listed Columbus Ohio — —
Not listed Burlington Vermont — —
Not listed Kirkland Washington — —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 55 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01093326, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Mar 30, 2025 · Synced Oct 19, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT01093326 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →