A Phase II/III Randomized, Double-blind, Placebo-controlled, Multicenter Study to Determine the Efficacy and Safety of ABC008 in the Treatment of Subjects with Inclusion Body Myositis
Details
Age
Adult
Type of Study
Treatment
Locations
Outpatient CTRC
Principal Investigator
Stacy Dixon, MD, PhD
Study ID
Protocol Number: 23-0008
Categories
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