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Clinical Trial Summary

The primary objective of the study is to characterize the persistence to therapy in participants with relapsing forms of multiple sclerosis (RMS) treated with diroximel fumarate (DRF) in routine clinical practice. The secondary objectives of the study are to assess short-term persistence to treatment; to assess long-term persistence on treatment; to assess the effect of DRF on relapses; to assess the impact of DRF on cognition; to assess the impact of DRF on participant reported outcomes (PROs); to assess the impact of DRF on disability; to assess treatment satisfaction with DRF; to explore the real-world safety profile of DRF (i.e., gastrointestinal [GI] tolerability, lymphocyte dynamics, adverse events [AEs] leading to discontinuation, and serious adverse events [SAEs].


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04948606
Study type Observational
Source Biogen
Contact
Status Terminated
Phase
Start date December 9, 2021
Completion date April 14, 2023

See also
  Status Clinical Trial Phase
Terminated NCT04746976 - Study of Diroximel Fumarate in the Real-World Setting