BEYOND Pilot Study

NCT00893217 · Status: COMPLETED · Phase: PHASE2 · Type: INTERVENTIONAL · Enrollment: 71

Last updated 2009-11-09

No results posted yet for this study

Summary

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

Conditions

Interventions

DRUG

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

250 mcg

DRUG

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

500 mcg

Sponsors & Collaborators

Principal Investigators

  • Bayer Study Director · Bayer

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
55 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2002-11-30
Completion
2003-06-30

Countries

  • United States

Study Locations

More Related Trials

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 NCT00893217 on ClinicalTrials.gov