Extension of Prior Study Evaluating Safety and Tolerability of Two Doses of Betaseron® to Treat Relapsing-remitting Multiple Sclerosis

PHASE2CompletedINTERVENTIONAL
Enrollment

63

Participants

Timeline

Start Date

June 30, 2003

Primary Completion Date

January 31, 2008

Study Completion Date

January 31, 2008

Conditions
Multiple Sclerosis, Relapsing-Remitting
Interventions
DRUG

Interferon beta 1b (Betaseron, BAY86-5046)

250 mcg administered s.c.(subcutaneous) every other day

DRUG

Interferon beta 1b (Betaseron, BAY86-5046)

250 mcg administered s.c. every other day (for patients having received 500 mcg before)

DRUG

Interferon beta 1b (Betaseron, BAY86-5046)

500 mcg administered s.c. every other day

DRUG

Interferon beta 1b (Betaseron, BAY86-5046)

500 mcg administered s.c. every other day (for patients having received 250 mcg before)

Trial Locations (17)

11794

Stony Brook

20037

Washington D.C.

27157

Winston-Salem

27262

High Point

27710

Durham

37212

Nashville

37232

Nashville

40202

Louisville

43221

Columbus

48109

Ann Arbor

60637

Chicago

66160

Kansas City

89509

Reno

94117

San Francisco

90095-1721

Los Angeles

30309-1465

Atlanta

48109-0022

Ann Arbor

Sponsors

Lead Sponsor

All Listed Sponsors
lead

Bayer

INDUSTRY