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

No results posted yet for this study

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

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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Entities

Companies

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 NCT01076595 on ClinicalTrials.gov