NASH Cirrhosis Trial: Evaluating a Combination of Drugs and Their Effects on Patients with NASH and Associated Cirrhosis

Clinical Trial Title

Study Evaluating the Safety and Efficacy of Semaglutide, and the Fixed-Dose Combination of Cilofexor and Firsocostat, Alone and in Combination, in Subjects with Compensated Cirrhosis (F4) due to Nonalcoholic Steatohepatitis (NASH)

National Clinical Trial Number:


Contact Information

Clinical Trial Protocol Description:

This phase 2, randomized, double-blind, double-dummy, placebo-controlled study is looking at the safety and efficacy of semaglutide and the fixed-dose combination of cilofexor and firsocostat, alone and in combination, in individuals with NASH and associated cirrhosis. There is a placebo group as well in this study.

Clinical Trial Eligibility Criteria:

In order to participate you must meet the following criteria:

  • Have cirrhosis due to NASH as seen on a liver biopsy.
  • Have a platelet count greater than or equal to 125,000/uL.
  • Not have type 1 diabetes.
  • Not be taking a diabetic medication from the GLP-1 drug class.

This is a partial list of eligibility requirements. To inquire about your eligibility, please call the contact number provided. If you wish to inquire via email, please include the title of the study in your message.

Study Details

Clinical Trial Investigator

Nikunj Shah

Contact Information

Diana Goldman

Clinical Trial Location

Rush University Medical Center


Rush University Medical Center

1620 W Harrison St
Chicago, IL 60612

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