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A Study of CRV431 Dosed Once Daily in NASH Induced F2 and F3 Subjects

A Study of CRV431 Dosed Once Daily in NASH Induced F2 and F3 Subjects

Recruiting
18-75 years
All
Phase 2
  • Simplified description (AI rewritten)
  • Technical description (Original)

This is a randomized, single-blind, placebo-controlled, once daily (QD) dose study of CRV431 in presumed NASH F2/F3 subjects. Study will evaluate the safety and tolerability of a once daily 75mg dose of CRV431 compared to placebo over 28 days of dosing. Pharmacokinetic parameters of CRV431 and its major metabolites and fraction unbound will also be evaluated. Non-invasive antifibrotic bio-markers will be collected and quantified from presumed NASH F2/F3 subjects dosed with 75mg CRV431 or placebo.

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Study details
    Cirrhosis
    NASH - Nonalcoholic Steatohepatitis
    NAFLD - Nonalcoholic Fatty Liver Disease

NCT04480710

Hepion Pharmaceuticals, Inc.

19 February 2024

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