A Multicenter, Randomized, Double-blind, Placebo-Controlled Trial of Emricasan (IDN- 6556), an Oral Caspase Inhibitor, in Subjects with Non-alcoholic Steatohepatitis (NASH) Fibrosis
A study for patients with non-alcoholic steatohepatitis (NASH) fibrosis using study drug Emricasan
Sponsor: Conatus Pharmaceuticals Inc.
Enrolling: Male and Female Patients
IRB Number: AAAQ6953
U.S. Govt. ID: NCT02686762
Contact: Theresa Lukose: 212-305-6758 / tt2103@cumc.columbia.edu
Additional Study Information: This study is for patients with non-alcoholic steatohepatitis (NASH) fibrosis in which there is too much fat in the liver causing inflammation and fibrosis. This condition is similar to the type of liver damage that occurs from too much alcohol use, but is not primarily caused by alcohol use. The main purpose of the study is to test whether a drug called emricasan (IDN-6556) will decrease the fat, inflammation, and fibrosis in the liver. Subjects in this study will have a 67% (2 in 3) chance of receiving emricasan and a 33% (1 in 3) chance of receiving placebo.
This study is closed
Investigator
Julia Wattacheril, MD, MPH
Do You Qualify?
Have you been diagnosed with non-alcoholic steatohepatitis (NASH) fibrosis? Yes No
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Place Holder




For more information, please contact:
Theresa Lukose
tt2103@cumc.columbia.edu
212-305-6758