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Completed Phase 2 Interventional Results available

Study of EYP-1901 in Patients With Nonproliferative Diabetic Retinopathy (NPDR)

ClinicalTrials.gov ID: NCT05383209

Public ClinicalTrials.gov record NCT05383209. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 21, 2026, 11:48 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Phase 2, Multicenter, Prospective, Double-masked, Parallel Study of EYP-1901, a Tyrosine Kinase Inhibitor (TKI), Compared to Sham for the Improvement of Moderately Severe to Severe Nonproliferative Diabetic Retinopathy (NPDR)

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

A prospective, randomized, double-masked study that evaluated the ocular efficacy and safety of two doses of the EYP-1901 intravitreal (IVT) insert compared to sham.

Study identification

NCT ID
NCT05383209
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
EyePoint Pharmaceuticals, Inc.
Industry
Enrollment
77 participants

Conditions and interventions

Interventions

Drug · Other

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Sep 28, 2022 (Actual)
Primary completion
Feb 12, 2024 (Actual)
Completion
May 6, 2024 (Actual)
Last update posted
Aug 15, 2025

2022 – 2024

United States locations

U.S. sites
36
U.S. states
19
U.S. cities
36
Facility City State ZIP Site status
EyePoint Investigative Site Phoenix Arizona 85020 —
EyePoint Investigative Site Huntington Beach California 92647 —
EyePoint Investigative Site Oxnard California 93036 —
EyePoint Investigative Site Palm Desert California 92211 —
EyePoint Investigative Site Pasadena California 90041 —
EyePoint Investigative Site Poway California 92064 —
EyePoint Investigative Site Sacramento California 95825 —
EyePoint Investigative Site Danbury Connecticut 06810 —
EyePoint Investigative Site Clearwater Florida 33761 —
EyePoint Investigative Site Melbourne Florida 32901 —
EyePoint Investigative Site Miami Florida 33143 —
EyePoint Investigative Site Winter Haven Florida 33880 —
EyePoint Investigative Site Lemont Illinois 60439 —
EyePoint Investigative Site Indianapolis Indiana 46290 —
EyePoint Investigative Site Lenexa Kansas 66215 —
EyePoint Investigative Site Baltimore Maryland 21209 —
EyePoint Investigative Site Hagerstown Maryland 21740 —
EyePoint Investigative Site Springfield Massachusetts 01107 —
EyePoint Investigative Site Reno Nevada 89502 —
EyePoint Investigative Site Bloomfield New Jersey 07003 —
EyePoint Investigative Site Toms River New Jersey 08755 —
EyePoint Investigative Site Great Neck New York 11021 —
EyePoint Investigative Site Erie Pennsylvania 16501 —
EyePoint Investigative Site Florence South Carolina 29501 —
EyePoint Investigative Site Ladson South Carolina 29456 —
EyePoint Investigative Site Rapid City South Dakota 57701 —
EyePoint Investigative Site Germantown Tennessee 38138 —
EyePoint Investigative Site Abilene Texas 79606 —
EyePoint Investigative Site Austin Texas 78705 —
EyePoint Investigative Site Houston Texas 78240 —
EyePoint Investigative Site McAllen Texas 78503 —
EyePoint Investigative Site Plano Texas 75075 —
EyePoint Investigative Site San Antonio Texas 78247 —
EyePoint Investigative Site The Woodlands Texas 77384 —
EyePoint Investigative Site Lynchburg Virginia 24502 —
EyePoint Investigative Site Bellevue Washington 98004 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT05383209, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Aug 15, 2025 · Synced Oct 21, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT05383209 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →