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RECRUITING
NCT04661358
PHASE3

Fenofibrate for Prevention of DR Worsening

Sponsor: Jaeb Center for Health Research

View on ClinicalTrials.gov

Summary

This randomized trial will evaluate the effect of fenofibrate compared with placebo for prevention of diabetic retinopathy (DR) worsening through 6 years of follow-up in eyes with mild to moderately severe non-proliferative DR (NPDR) and no CI-DME at baseline. In addition to evaluating efficacy, this study aims to evaluate the feasibility of a model for ophthalmologists to prescribe or collaborate with a primary care provider such as an internist/endocrinologist to prescribe and monitor the drug safely. If this study demonstrates that fenofibrate is effective for reducing the onset of proliferative diabetic retinopathy (PDR) or and the results are adopted by the community of retina specialists, a new strategy to prevent vision threatening complications of diabetes could be widely adopted. Widespread use of an oral agent effective at reducing worsening of DR would decrease the numbers of patients who undergo more invasive and much more expensive treatment for DR and who are consequently at risk for side effects that adversely affect visual function. This study will also assess the relationship of glycemic variability, as measured by continuous glucose monitoring with DR outcomes. Ancillary studies will characterize functional and structural outcomes in this cohort.

Official title: A Randomized Clinical Trial Evaluating Fenofibrate for Prevention of Diabetic Retinopathy Worsening

Key Details

Gender

All

Age Range

18 Years - 80 Years

Study Type

INTERVENTIONAL

Enrollment

560

Start Date

2021-03-05

Completion Date

2029-12

Last Updated

2025-11-13

Healthy Volunteers

No

Interventions

DRUG

Fenofibrate

Participants begin with a dose of either 160mg or 54mg fenofibrate, based on eGFR value at screening, taken once daily with food. The dose may be adjusted during follow-up based on protocol guidelines.

OTHER

Placebo

Participants begin with a dose of either 160mg or 54mg placebo, based on eGFR value at screening, taken once daily with food. The dose may be adjusted during follow-up based on protocol guidelines.

Locations (66)

Kent W. Small, MD, AMC

Glendale, California, United States

Salehi Retina Institute Inc.

Huntington Beach, California, United States

Loma Linda University

Loma Linda, California, United States

UCLA Stein Eye Institute

Pasadena, California, United States

Regents of the University of California, Davis, DBA University of California, Davis

Sacramento, California, United States

The Regents of the University of California, San Francisco

San Francisco, California, United States

National Ophthalmic Research Institute

Fort Myers, Florida, United States

University of Florida- Jacksonville

Jacksonville, Florida, United States

Florida Retina Institute, James A. Staman, MD, PA- Jacksonville

Jacksonville, Florida, United States

Florida Retina Consultants

Lakeland, Florida, United States

Florida Retina Institute, James A. Staman, MD, PA- Orlando

Orlando, Florida, United States

Southeast Eye Institute, P.A. dba Eye Associates of Pinellas

Pinellas Park, Florida, United States

Retina Vitreous Consultants, LLP

Sarasota, Florida, United States

Sarasota Retina Institute

Sarasota, Florida, United States

SEASHORE RETINA LLC DBA Retina Specialists of Tampa

Wesley Chapel, Florida, United States

Southeast Retina Center, P.C.

Augusta, Georgia, United States

Marietta Eye Clinic

Marietta, Georgia, United States

Thomas Eye Group

Sandy Springs, Georgia, United States

Northwestern University

Chicago, Illinois, United States

Rush University Medical Center

Chicago, Illinois, United States

UIC - Dept of Ophthalmology & Visual Sciences

Chicago, Illinois, United States

Illinois Retina Associates SC - Oak Park Site

Oak Park, Illinois, United States

Midwest Eye Institute

Indianapolis, Indiana, United States

John Kenyon American Eye Institute, LLC

New Albany, Indiana, United States

Wolfe Eye Clinic-Cedar Rapids

Hiawatha, Iowa, United States

Wolfe Clinic, P.C.- West Des Moines

West Des Moines, Iowa, United States

Mid-America Retina Consultants, P.A.

Overland Park, Kansas, United States

University of Kansas Medical Center Research Institute, Inc.

Prairie Village, Kansas, United States

Joseph E. Humble and Raymond Haik PTRS DBA Eye Assoc of Northeast Louisiana

West Monroe, Louisiana, United States

Elman Retina Group, P.A.

Baltimore, Maryland, United States

Valley Eye Physicians and Surgeons

Ayer, Massachusetts, United States

Boston Medical Center Corporation

Boston, Massachusetts, United States

Joslin Diabetes Center

Boston, Massachusetts, United States

Henry Ford Health System

Detroit, Michigan, United States

Foundation for Vision Research and Retina Specialists of Michigan, P.C.

Grand Rapids, Michigan, United States

Vitreo-Retinal Associates

Grand Rapids, Michigan, United States

Retina Center, PA DBA Retina Center of Minnesota

Minneapolis, Minnesota, United States

Mayo Clinic

Rochester, Minnesota, United States

The Curators of the University of Missouri

Columbia, Missouri, United States

Washington University Ophthalmology

St Louis, Missouri, United States

Retina Research Institute, LLC

St Louis, Missouri, United States

Retina-Vitreous Surgeons of Central NY, PC

Liverpool, New York, United States

MaculaCare

New York, New York, United States

Retina Associates of Western NY, P.C.

Rochester, New York, United States

Pamela Weber, MD/Island Retina

Shirley, New York, United States

University of North Carolina at Chapel Hill

Chapel Hill, North Carolina, United States

The Cleveland Clinic Foundation DBA Cleveland Clinic Lerner College of Medicine

Cleveland, Ohio, United States

Dean A. McGee Eye Institute

Oklahoma City, Oklahoma, United States

Verum Research LLC

Eugene, Oregon, United States

Oregon Health & Science University

Portland, Oregon, United States

Retina Consultants, LLC

Salem, Oregon, United States

Cascade Medical Research Institute, LLC

Springfield, Oregon, United States

Retina-Vitreous Consultants, Inc.

Monroeville, Pennsylvania, United States

Pittsburg Clinical Trial Consortium

Sewickley, Pennsylvania, United States

Southeastern Retina Associates, P.C.

Knoxville, Tennessee, United States

Vanderbilt Eye Institute

Nashville, Tennessee, United States

Austin Research Center for Retina

Austin, Texas, United States

Austin Retina Associates

Austin, Texas, United States

Retina Consultants of Texas

Beaumont, Texas, United States

Retina Consultants of Texas, PA

Bellaire, Texas, United States

Baylor College of Medicine, Baylor Eye Physicians and Surgeons

Houston, Texas, United States

Texas Retina Associates

Lubbock, Texas, United States

Retinal Consultants of San Antonio

San Antonio, Texas, United States

University of Washington

Seattle, Washington, United States

Gunderson Health System

La Crosse, Wisconsin, United States

Eye Clinic of Wisconsin

Wausau, Wisconsin, United States