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New drug shows promise for fatty liver in early trial

NCT ID NCT04006145

First seen Feb 05, 2026 · Last updated Jun 20, 2026 · Updated 22 times

Summary

This phase 2 trial tested the drug elobixibat in 47 adults with nonalcoholic fatty liver disease (NAFLD) or its more severe form, NASH. The study compared elobixibat to a placebo to see if it could lower LDL cholesterol and improve liver health over 16 weeks. The trial is now complete, and results will help determine if larger studies are warranted.

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This is a summary of the original study . Summaries may miss details or leave out important information. Before applying or accepting participation, make sure you have read and understood the full study. Curemydisease.com takes no responsibility whatsoever for anything missed, misunderstood, or acted upon as a result of our summary — we know it does not capture everything.

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Contacts and locations

Locations

  • American Research Corporation at the Texas Liver Institute

    San Antonio, Texas, 78215, United States

  • Guardian Angel Research Center, Inc.

    Tampa, Florida, 33614, United States

  • Hope Clinical Research

    Canoga Park, California, 91303, United States

  • Inland Empire Clinical Trials, LLC

    Rialto, California, 92377, United States

  • Integrity Clinical Research, LLC

    Doral, Florida, 33166, United States

  • Mercy Medical Center

    Baltimore, Maryland, 21202, United States

  • Nature Coast Clinical Research

    Inverness, Florida, 34452, United States

  • Peak Gastroenterology Associates

    Colorado Springs, Colorado, 80907, United States

  • University of Washington

    Seattle, Washington, 98195, United States

  • Virginia Commonwealth University

    Richmond, Virginia, 23298, United States

What this could mean

Our plain-language read of the trial. This is informational only — not medical advice or a prediction.

Active substance

elobixibat

What this could lead to

If successful, elobixibat could offer a new way to manage NAFLD/NASH by lowering cholesterol and potentially reducing liver fat.

What could go wrong

This is a small, early-phase trial with only 47 participants. The primary endpoint is a cholesterol marker, not a direct measure of liver disease improvement. Results may not confirm benefit or safety.

Conditions

The condition(s) this trial relates to.

metabolic dysfunction-associated steatotic liver disease

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.