Safety, Tolerability, and Efficacy of Monotherapy and Combination Regimens in Participants With Nonalcoholic Steatohepatitis (NASH)
Completed · Phase 2
Conditions studied: Nonalcoholic Steatohepatitis
In brief
The primary objective of this study is to evaluate the safety and tolerability of study drug(s) in participants with nonalcoholic steatohepatitis (NASH).
Key facts
- Study ID
- NCT03987074
- Run by
- Gilead Sciences
- People needed
- 109
- Starts
- 2019-07-29
- Expected to finish
- 2020-07-13
- Last updated by the study team
- 2021-07-15
Who can join
Age: 18 and older, up to 75. Sex: any. Healthy volunteers: not accepted.
Where it is running
- Institute for Liver Health - Arizona Liver Health — Chandler, Arizona, United States
- Southern California Research Centers — Coronado, California, United States
- University of California San Diego (UCSD) — La Jolla, California, United States
- Ruane Clinical Research Group, Inc — Los Angeles, California, United States
- Cedars Sinai Medical Center — Los Angeles, California, United States
- Inland Empire Clinical Trials, LLC — Rialto, California, United States
- Medical Associates Research Group — San Diego, California, United States
- Gastrointestinal Specialists of Georgia — Marietta, Georgia, United States
- Beth Israel Deaconess Medical Center — Boston, Massachusetts, United States
- Jubilee Clinical Research, Inc. — Las Vegas, Nevada, United States
- Northwell Health — Manhasset, New York, United States
- Gastro One — Huntersville, North Carolina, United States
- University Gastroenterology — Providence, Rhode Island, United States
- Gastro One — Germantown, Tennessee, United States
- Quality Medical Research, PLLC — Nashville, Tennessee, United States
- Texas Clinical Research Institute — Arlington, Texas, United States
- The Liver Institute at Methodist Dallas Medical Center — Dallas, Texas, United States
- American Research Corporation — San Antonio, Texas, United States
Full record on ClinicalTrials.gov
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