Betaferon Use in Children and Adolescents With Multiple Sclerosis

NCT03577977 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 70

Last updated 2018-07-11

No results posted yet for this study

Summary

The objective of this study is to determine efficacy, safety and tolerability of interferon beta-1b for multiple sclerosis (MS) in children and adolescents

Conditions

Interventions

DRUG

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

Betaferon was injected subcutaneously as prescribed by the treating physician.

Sponsors & Collaborators

Principal Investigators

  • Bayer Study Director · Bayer

Eligibility

Max Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2008-06-01
Primary Completion
2009-04-15
Completion
2009-04-15

Countries

  • Russia

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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 NCT03577977 on ClinicalTrials.gov