This is a double-blind, placebo controlled multicenter Phase III study. The purpose of the study is to determine whether 20 mg of Copolymer I administered by subcutaneous injection daily for 24 months to patients with relapsing-remitting multiple sclerosis reduces the number of relapses as compared to placebo. It also compares the safety and tolerance of Copolymer I and placebo.

Agency
National Institute of Health (NIH)
Institute
National Center for Research Resources (NCRR)
Type
General Clinical Research Centers Program (M01)
Project #
2M01RR002558-08A1
Application #
3788653
Study Section
Project Start
Project End
Budget Start
Budget End
Support Year
8
Fiscal Year
1993
Total Cost
Indirect Cost
City
Houston
State
TX
Country
United States
Zip Code
77225
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