Study to Assess Effect and Safety of High Dose of Biotin (Qizenday®) in Progressive Multiple Sclerosis
NCT03302806 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 103
Last updated 2021-09-21
Summary
The purpose of this observational study is to collect efficacy and safety data in real life condition within the first year of treatment in patients with progressive multiple receiving a daily dose of biotine of 300 mg.
Conditions
Interventions
- OTHER
-
Non interventional Study
Sponsors & Collaborators
-
Nantes University Hospital
lead OTHER
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2016-06-29
- Primary Completion
- 2017-10-04
- Completion
- 2018-10-24
Countries
- France
Study Locations
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