drugset / Trial / NCT05201638

Study to Evaluate the Efficacy, Safety and Tolerability of IMU-838 in Patients With Relapsing Multiple Sclerosis

NCT05201638

Phase 3 Active not recruiting 1100 enrolled Immunic AG
RandomizedParallel-groupQuadruple-blindTreatment

Summary

Multi-Center, Randomized, Double-Blinded Phase 3 Study to Evaluate the Efficacy, Safety, and Tolerability of IMU-838 versus Placebo in Adults with Relapsing Multiple Sclerosis (ENSURE-2)

Timeline

Start
2022-01-12
Primary completion
2026-11
Completion
2033-10

Drugs

EvaluationDrugModalityDoseRoute
Subject Vidofludimus Small molecule 15 mg Oral
Subject Vidofludimus Small molecule 30 mg Oral