drugset / Trial / NCT03232073

Long-term Extension to Study AC-058B301 to Investigate Safety, Tolerability and Disease Control of Ponesimod 20 mg in Patients With Relapsing Multiple Sclerosis

NCT03232073

Phase 3 Completed 877 enrolled Actelion
NaSingle-groupOpen-labelTreatment

Summary

The study AC-058B301 (OPTIMUM; NCT02425644) has been designed to investigate the efficacy, safety and tolerability of ponesimod in subjects with relapsing multiple sclerosis (RMS). The AC-058B303 study is the long-term extension for the core study AC-058B301. The purpose of this long term extension of the core study AC-058B301 is to characterize the long-term safety, tolerability, and control of disease of ponesimod 20 mg in subjects with RMS.

Timeline

Start
2017-07-05
Primary completion
2024-01-16
Completion
2024-01-16

Drugs

EvaluationDrugModalityDoseRoute
Subject Ponesimod Small molecule 20 mg Oral

Indications