A Phase 2, Randomized, Double-Blind, Placebo-Controlled, Multicenter, Dose-Finding Study to evaluate the efficacy and safety of CC-90001 in subjects with Non-Alcoholic Steatohepatitis (NASH) and Stage 3 or Stage 4 Liver Fibrosis
Principal Investigator(s)
Email for information
Funded by
Geneva
Research Start Date
Status
Inactive
The effect of oral (PO) CC-90001, administered once daily (QD), compared with placebo, will be evaluated in subjects with NASH and Stage 3 fibrosis and explored in subjects with NASH and Stage 4 fibrosis
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