PROMINENT-Eye Ancillary Study (Protocol AD)



Status:Terminated
Conditions:Ocular, Ocular, Diabetes
Therapuetic Areas:Endocrinology, Ophthalmology
Healthy:No
Age Range:18 - Any
Updated:4/6/2019
Start Date:January 15, 2018
End Date:April 3, 2019

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PROMINENT-Eye Ancillary Study: Diabetic Retinopathy Outcomes in a Randomized Trial of Pemafibrate Versus Placebo (Protocol AD)

Despite improved glycemic and systemic control for many patients with diabetes, over the past
several decades, diabetic retinopathy (DR) develops and progresses in a large proportion of
patients, and visual loss from diabetic eye complications continues to be a leading cause of
blindness in the US and other developed countries worldwide. Thus, even a modest ability to
prevent DR onset or to slow DR worsening might substantially reduce the number of patients at
risk for diabetes-related vision loss worldwide. Widespread use of an oral agent effective at
reducing worsening of DR might also decrease the numbers of patients who undergo treatment
for DR and diabetic macular edema (DME) and who are consequently at risk for side effects
that adversely affect visual function. Two major studies of fenofibrate, the Fenofibrate
Intervention and Event Lowering in Diabetes (FIELD) and The Action to Control Cardiovascular
Risk in Diabetes (ACCORD)-eye study, have demonstrated clinically important reduction in
progression of retinopathy in patients with diabetes assigned to fibrate compared with
placebo. However, despite the positive clinical trial results, fenofibrate has not gained
wide acceptance as a preventive agent by either ophthalmologists or primary diabetes care
providers. Thus, it is important to provide further evidence demonstrating whether or not
selectively increasing peroxisome proliferator-activated receptor alpha (PPARα) activity
reduces progression of retinopathy in patients with diabetes and non-proliferative diabetic
retinopathy at baseline. Pemafibrate is a more potent and selective PPARα modulator than
fenofibrate. Its efficacy is currently being evaluated in the Pemafibrate to Reduce
Cardiovascular OutcoMes by Reducing Triglycerides IN patiENts With diabeTes (PROMINENT) study
for prevention of cardiovascular events in patients with type 2 diabetes. Given the large
study cohort with a substantial proportion likely to have DR and the multi-year duration of
the PROMINENT trial, this study represents a unique opportunity to assess effects of chronic
PPARα activation through pemafibrate therapy on DR outcomes.

Primary Study Objective: To assess whether treatment with pemafibrate (0.2 mg orally BID)
compared with placebo reduces the hazard rate of diabetic retinopathy worsening in adults
with type 2 diabetes and diabetic retinopathy without neovascularization in at least one eye
who are participating in the parent PROMINENT trial.


Inclusion Criteria:

- Already randomized at US or Canadian sites in the PROMINENT study

- Ability to cooperate with dilated ophthalmic examination and imaging procedures

- At least one eye meets the following study eye inclusion criteria:

1. Early Treatment Diabetic Retinopathy Study (ETDRS) Diabetic Retinopathy Severity
level between 20 and 53 (minimal to severe non-proliferative diabetic retinopathy
(NPDR)), inclusive, on color fundus photographs confirmed by central Reading
Center grading.

Exclusion Criteria:

- Study eye exclusion criteria are:

a. Neovascularization present. b. Current central-involved diabetic macular edema (DME
based on optical coherence tomography (OCT) central subfield thickness (CST) i. Zeiss
Cirrus: CST ≥ 290µm in women or ≥ 305µm in men ii. Heidelberg Spectralis: CST ≥ 305µm
in women or ≥ 320µm in men c. Known major non-diabetic intraocular pathology that in
the opinion of the investigator would substantially and adversely affect visual acuity
or lead to ocular neovascularization during the course of the study d. Anticipated
need for intravitreous anti-vascular endothelial growth factor (VEGF), intravitreous
corticosteroid, or pan-retinal photocoagulation (PRP) in the next 6 months following
randomization e. History of intravitreous anti-VEGF or corticosteroid treatment within
the prior year for any indication.

f. History of intraocular surgery within prior 4 months or anticipated within the next
6 months following randomization g. Any history of PRP or vitrectomy h. History of
yttrium aluminum garnet (YAG) capsulotomy performed within 2 months prior to screening
i. Aphakia j. Known substantial media opacities that would preclude successful imaging
We found this trial at
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New Albany, Indiana 47150
Phone: 800-965-3937
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One Joslin Place
Boston, Massachusetts 02215
617-309-2400
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Joslin Diabetes Center Joslin Diabetes Center, located in Boston, Massachusetts, is the world's largest diabetes...
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Chicago, Illinois 60611
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