drugset / Trial / NCT04338061
Study of Evobrutinib in Participants With RMS (evolutionRMS 2)
Phase 3
Terminated
1166 enrolled
Merck Healthcare KGaA, Darmstadt, Germany, an affiliate of Merck KGaA, Darmstadt, Germany
EMD Serono Research & Development Institute, Inc. · collab
RandomizedParallel-groupQuadruple-blindTreatment
Summary
The study is to evaluate the efficacy and safety of evobrutinib administered orally twice daily versus Teriflunomide (Aubagio®), administered orally once daily in participants with Relapsing Multiple Sclerosis (RMS). Participants who complete the double-blind treatment period (DBTP) and double-blind extension period (DBEP) prior to approval of a separate long-term follow-up study in their country will get an option for evobrutinib treatment continuation through a 96-week open-label extension (OLE) period.
Timeline
- Start
- 2020-07-02
- Primary completion
- 2023-10-02
- Completion
- 2024-03-19
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Evobrutinib | Small molecule | 45 mg | Oral |
| Comparator | Teriflunomide | Small molecule | 14 mg | Oral |