A Study of the Efficacy and Safety of CF102 in the Treatment of Non-Alcoholic Fatty Liver Disease
NCT02927314 · Status: COMPLETED · Phase: PHASE2 · Type: INTERVENTIONAL · Enrollment: 60
Last updated 2020-03-17
Summary
This is a multicenter, randomized, double-blind, placebo-controlled clinical trial in subjects with NAFLD and NASH.
Conditions
- Non-alcoholic Steatohepatitis (NASH)
Interventions
- DRUG
-
CF102
orally q12h
- DRUG
-
orally q12h
Sponsors & Collaborators
-
Can-Fite BioPharma
lead INDUSTRY
Principal Investigators
-
Michael H Silverman, MD · Can-Fite BioPharma Ltd
Study Design
- Allocation
- RANDOMIZED
- Purpose
- TREATMENT
- Masking
- TRIPLE
- Model
- PARALLEL
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2017-11-27
- Primary Completion
- 2020-03-01
- Completion
- 2020-03-01
Countries
- Israel
Study Locations
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