A Study to Evaluate the Safety, Tolerability & Efficacy of MSDC-0602K in Patients With NASH

Completed · Phase 2 · Has a placebo group

Conditions studied: Non-alcoholic Fatty Liver Disease, Non-alcoholic Steatohepatitis, NASH - Nonalcoholic Steatohepatitis

In brief

This is a randomized, double-blinded study of three doses of MSDC-0602K or placebo given orally once daily to subjects with biopsy proven NASH with fibrosis and no cirrhosis.

Key facts

Study ID

NCT02784444

Run by

Cirius Therapeutics, Inc.

People needed

392

Starts

2016-09-14

Expected to finish

2019-06-01

Last updated by the study team

2020-09-16

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

Where it is running

• Study site — Chandler, Arizona, United States
• Study site — Tucson, Arizona, United States
• Study site — Chula Vista, California, United States
• Study site — Fresno, California, United States
• Study site — Garden Grove, California, United States
• Study site — Huntington Park, California, United States
• Study site — La Mesa, California, United States
• Study site — Los Angeles, California, United States
• Study site — Los Angeles, California, United States
• Study site — Poway, California, United States
• Study site — Rialto, California, United States
• Study site — San Diego, California, United States
• Study site — Englewood, Colorado, United States
• Study site — Gainesville, Florida, United States
• Study site — Hialeah, Florida, United States
• Study site — Inverness, Florida, United States
• Study site — Lakewood Rch, Florida, United States
• Study site — Miami Lakes, Florida, United States
• Study site — Wellington, Florida, United States
• Study site — Marietta, Georgia, United States
• Study site — Indianapolis, Indiana, United States
• Study site — Bastrop, Louisiana, United States
• Study site — New Orleans, Louisiana, United States
• Study site — New Orleans, Louisiana, United States
• Study site — West Monroe, Louisiana, United States

Full record on ClinicalTrials.gov

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