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Completed Phase 2 Interventional Results available

The TIME-2b Study: A Study of AKB-9778 (Razuprotafib), a Novel Tie 2 Activator, in Patients With Non-Proliferative Diabetic Retinopathy (NPDR)

ClinicalTrials.gov ID: NCT03197870

Public ClinicalTrials.gov record NCT03197870. 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 22, 2026, 8:03 PM EDT

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

Official title

Phase 2 Double-Masked, Placebo-Controlled Study to Assess the Safety and Efficacy of Subcutaneously Administered AKB-9778 (Razuprotafib)15mg Once Daily or 15mg Twice Daily for 12 Months in Patients With Moderate to Severe Non-Proliferative Diabetic Retinopathy

Brief summary

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

The purpose of this study is to evaluate the safety and efficacy of subcutaneously administered AKB-9778 15mg once daily or 15mg twice daily for 12 months in patients with moderate to severe non-proliferative diabetic retinopathy (NPDR).

Study identification

NCT ID
NCT03197870
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
EyePoint Pharmaceuticals, Inc.
Industry
Enrollment
167 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years to 80 Years
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
Jun 9, 2017 (Actual)
Primary completion
Jan 9, 2019 (Actual)
Completion
Feb 9, 2019 (Actual)
Last update posted
Jun 27, 2023

2017 – 2019

United States locations

U.S. sites
53
U.S. states
23
U.S. cities
50
Facility City State ZIP Site status
Arizona Retina and Vitreous Consultants Phoenix Arizona 85021 —
Retinal Research Institute Phoenix Arizona 85053 —
Retina Institute of California Arcadia California 91007 —
California Retina Consultants Bakersfield California 93309 —
Retina Vitreous Associates Medical Group Beverly Hills California 90211 —
Retina Consultants of Orange County Fullerton California 92835 —
Ophthalmic Clinical Trials San Diego Oceanside California 92056 —
Stanford Palo Alto California 94303 —
California Retina Consultants Santa Barbara California 93103 —
California Retina Consultants Santa Maria California 93454 —
Retina Consultants of Southern Colorado Colorado Springs Colorado 80909 —
Colorado Retina Associates Golden Colorado 80401 —
Rand Eye Institute Deerfield Beach Florida 33064 —
Center for Retina and Macular Disease Lakeland Florida 33805 —
Retina Specialty Institute Pensacola Florida 32503 —
Southeast Retina Center Augusta Georgia 30909 —
Georgia Retina Marietta Georgia 30060 —
University Retina Oak Forest Illinois 60452 —
Illinois Retina Associates Oak Park Illinois 60304 —
Midwest Eye Institute Indianapolis Indiana 46290 —
Wolfe Eye Clinic West Des Moines Iowa 50266 —
Central Plains Eye MDs Wichita Kansas 67226 —
Retina Associates of Kentucky Lexington Kentucky 40509 —
Johns Hopkins University School of Medicine Baltimore Maryland 212876 —
Cumberland Valley Retina Consultants PC Hagerstown Maryland 21740 —
Opthalmic Consultants of Boston Boston Massachusetts 02114 —
Specialty Eye Institute Jackson Michigan 49202 —
Sierra Eye Associates Reno Nevada 89502 —
Retina Center of New Jersey Bloomfield New Jersey 07003 —
New Jersey Retina Edison New Jersey 08820 —
Retinal and Ophthalmic Consultants P.C. Northfield New Jersey 08225 —
Eye Associates of New Mexico Albuquerque New Mexico 87109 —
Island Retina Shirley New York 11967 —
Retina Vitreous Surgeons of Central New York Syracuse New York 13224 —
Retina Associates of Cleveland Beachwood Ohio 44122 —
Cincinnati Eye Institute Cincinnati Ohio 45242 —
Retina Associates of Cleveland Middleburg Heights Ohio 44130 —
Retina Associates of Cleveland Youngstown Ohio 44505 —
Retina Vitreous Center Edmond Oklahoma 73013 —
Mid-Atlantic Retina Bethlehem Pennsylvania 18017 —
Tennessee Retina Nashville Tennessee 37203 —
Retina Research Institute of Texas Abilene Texas 79606 —
Texas Retina Associates Arlington Texas 76012 —
Austin Retina Associates Austin Texas 78705 —
Retina Research Center Austin Texas 78705 —
Texas Retina Associates Fort Worth Texas 76104 —
Valley Retina Institute Harlingen Texas 78550 —
Retina and Vitreous of Texas Houston Texas 77025 —
Retina Consultants of Houston Houston Texas 77030 —
Valley Retina Institute McAllen Texas 78503 —
Medical Center Ophthalmology Associates San Antonio Texas 78240 —
Retina Consultants of Houston The Woodlands Texas 77384 —
Spokane Eye Clinical Research Spokane Washington 99204 —

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 NCT03197870, 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 Jun 27, 2023 · Synced Oct 22, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT03197870 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →