BENEFIT Extension Study

NCT00544037 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 283

Last updated 2012-03-05

No results posted yet for this study

Summary

To assess the long-term effects of early therapeutic intervention, i.e. within two years following a first clinical demyelinating event suggestive of MS.

Conditions

Interventions

DRUG

Interferon beta-1b (Betaseron, BAY86-5046)

Standard Therapy for Multiple Sclerosis

Sponsors & Collaborators

Principal Investigators

  • Bayer Study Director · Bayer

Eligibility

Min Age
23 Years
Max Age
50 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2007-09-30
Primary Completion
2011-01-31
Completion
2011-01-31

Countries

  • Austria
  • Belgium
  • Canada
  • Czechia
  • Denmark
  • Finland
  • France
  • Germany
  • Hungary
  • Israel
  • Italy
  • Netherlands
  • Norway
  • Poland
  • Slovenia
  • Spain
  • Sweden
  • Switzerland

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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 NCT00544037 on ClinicalTrials.gov