Prospective, Multicenter Non Interventional Study to Evaluate Adherence to Betaferon Over a 2 Years Period
NCT01076595 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 73
Last updated 2015-07-03
Summary
The aim of the SEPLUS study is to evaluate the patients characteristics associated with adherence to Betaferon over a 24-month follow up period after the initiation of Betaferon in the BetaPlus program
Conditions
Interventions
- DRUG
-
Interferon beta-1b (Betaseron, BAY86-5046)
Betaferon 250 microgram
Sponsors & Collaborators
- lead INDUSTRY
Principal Investigators
-
Bayer Study Director · Bayer
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2010-05-31
- Primary Completion
- 2013-11-30
- Completion
- 2014-07-31
Countries
- France
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