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BEYOND Pilot Study

Multiple Sclerosis Clinical Trial

Official title:
Double-blind, Randomized, Parallel Group, Multicenter Study of the Safety and Tolerability of Betaseron 500 Mcg Subcutaneously Every Other Day and Betaseron 250 Mcg Subcutaneously Every Other Day for at Least 12 Weeks in Patients With RRMS

Clinical Trial Summary

The purpose of this study is to valuate safety and tolerability of Betaseron.

Clinical Trial Description

n/a

Study Design

Allocation: Randomized, Endpoint Classification: Safety Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator), Primary Purpose: Treatment

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT00893217
Study type Interventional
Source Bayer
Contact
Status Completed
Phase Phase 2
Start date November 2002
Completion date June 2003
View Details
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