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Clinical trial

Double-Blind, Placebo-Controlled, Randomized, Parallel Group, Multicenter Study to Evaluate Efficacy and Safety of 4 and 8 Million Units Betaferon®/Betaseron® (Interferon Beta-1b) Given Subcutaneously Every Other Day Over 24 Weeks in Patients With Chronic Viral Cardiomyopathy

NCT00185250 is registered in ClinicalTrials.gov with Bayer as lead sponsor.

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Registry record

As filed in ClinicalTrials.gov.

Title
Double-Blind, Placebo-Controlled, Randomized, Parallel Group, Multicenter Study to Evaluate Efficacy and Safety of 4 and 8 Million Units Betaferon®/Betaseron® (Interferon Beta-1b) Given Subcutaneously Every Other Day Over 24 Weeks in Patients With Chronic Viral Cardiomyopathy
Lead sponsor
Bayer
Phase
Phase 2
Overall status
Completed
Start date
December 31, 2002
Completion date
November 30, 2005
Enrollment
138 (actual)
Sites
31

Conditions

As the registry lists them; a condition with its own page is linked.