RecruitingPhase 1NCT05979389

Bicalutamide Therapy in Young Women With NAFLD and PCOS

Pilot Trial of Bicalutamide Versus Placebo in Reproductive-Aged Women With Nonalcoholic Fatty Liver Disease (NAFLD) and Polycystic Ovary Syndrome (PCOS)


Sponsor

University of California, San Francisco

Enrollment

50 participants

Start Date

Feb 14, 2024

Study Type

INTERVENTIONAL

Conditions

Summary

Nonalcoholic steatohepatitis (NASH), or fat-related liver inflammation and scarring is projected to be the leading cause of cirrhosis in the United States (U.S.) within the next few years. Women are at disproportionate risk for NASH, with approximately 15 million U.S. women affected. There is an urgent need to understand risk factors for NASH and its progression in women, and sex hormones may provide a missing link. This study will study the contribution of androgens to liver injury and progression in PCOS and mechanistic role of dysregulated lipid metabolism and visceral adiposity in this process. Such findings will provide the rationale for future efficacy studies evaluating selective androgen receptor (AR) antagonism for NASH in PCOS, or alternatively, the need to directly target visceral adiposity or lipid-specific pathways as part of a precision medicine approach to halt fibrosis progression in the nearly 5 million young women with PCOS and NAFLD in the U.S., who remain at increased risk for early onset and progressive liver disease.


Eligibility

Sex: FEMALEMin Age: 18 YearsMax Age: 42 Years

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying a drug called Bicalutamide 50 mg and a drug called Placebo for people with nafld and pcos. The study is currently recruiting participants at 1 location. People eligible for this study include women aged 18 Years to 42 Years.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DRUGBicalutamide 50 mg

Bicalutamide capsules will be prepared from U.S. Pharmacopeia grade powder at a dose of 50 mg

DRUGPlacebo

Matching placebo capsules of the same color, mass, and appearance to the bicalutamide capsules will be filled using microcrystalline cellulose powder.


Locations(1)

University of California San Francisco

San Francisco, California, United States

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NCT05979389


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