Observational Study of Persistence on Bafiertam Treatment in Routine Clinical Practice

NCT05978531 · Status: TERMINATED · Type: OBSERVATIONAL · Enrollment: 25

Last updated 2025-03-06

No results posted yet for this study

Summary

This is an open-label, multicenter, observational study of the adherence of patients with relapsing-remitting multiple sclerosis (RRMS) prescribed Bafiertam (monomethyl fumarate) as their treatment.

Conditions

  • Relapsing Remitting Multiple Sclerosis

Interventions

DRUG

Monomethyl Fumarate

95 mg oral capsule, 190 mg (2 x 95 mg) twice daily

Sponsors & Collaborators

  • Banner Life Sciences LLC

    lead INDUSTRY

Principal Investigators

  • Thomas Lategan, PhD · Banner Life Sciences

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2023-08-17
Primary Completion
2025-02-24
Completion
2025-02-24
FDA Drug
Yes

Countries

  • United States
  • Puerto Rico

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05978531 on ClinicalTrials.gov