drugset / Trial / NCT04410978

Relapsing Forms of Multiple Sclerosis (RMS) Study of Bruton's Tyrosine Kinase (BTK) Inhibitor Tolebrutinib (SAR442168) (GEMINI 1)

NCT04410978

Phase 3 Completed 974 enrolled Sanofi
RandomizedParallel-groupTriple-blindTreatment

Summary

Primary Objective: To assess efficacy of daily SAR442168 compared to a daily dose of 14 mg teriflunomide (Aubagio) measured by annualized adjudicated relapse rate (ARR) in participants with relapsing forms of MS Secondary Objective: To assess efficacy of SAR442168 compared to teriflunomide (Aubagio) on disability progression, MRI lesions, cognitive performance and quality of life To evaluate the safety and tolerability of daily SAR442168 To evaluate population pharmacokinetics (PK) of SAR442168 and relevant metabolites and its relationship to efficacy and safety To evaluate pharmacodynamics (PD) of SAR442168

Timeline

Start
2020-06-30
Primary completion
2024-07-15
Completion
2024-07-15

Drugs

EvaluationDrugModalityDoseRoute
Comparator Teriflunomide Small molecule 14 mg Oral
Subject Tolebrutinib Small molecule 60 mg Oral

Indications