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Completed Phase 2 Interventional Results available

Zimura Compared to Sham in Patients With Autosomal Recessive Stargardt Disease (STGD1)

ClinicalTrials.gov ID: NCT03364153

Public ClinicalTrials.gov record NCT03364153. 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, 5:56 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 2b Randomized, Double-masked, Controlled Trial to Establish the Safety and Efficacy of Zimura™ (Complement C5 Inhibitor) Compared to Sham in Subjects With Autosomal Recessive Stargardt Disease

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 avacincaptad pegol intravitreal injection compared to Sham in participants with autosomal recessive Stargardt disease 1 (STGD1).

Study identification

NCT ID
NCT03364153
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Enrollment
121 participants

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
18 Years to 60 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
Jan 12, 2018 (Actual)
Primary completion
Mar 31, 2025 (Actual)
Completion
Mar 31, 2025 (Actual)
Last update posted
Apr 15, 2026

2018 – 2025

United States locations

U.S. sites
17
U.S. states
13
U.S. cities
17
Facility City State ZIP Site status
Retinal Research Institute Phoenix Arizona 85053 —
Jules Stein Eye Institute/ David Geffen School of Medicine Los Angeles California 90095 —
VitreoRetinal Associates Gainesville Florida 32607 —
Retina Specialty Institute Pensacola Florida 32503 —
Wilmer Eye Institute, Johns Hopkins Baltimore Maryland 21287 —
Ophthalmic Consultants of Boston Boston Massachusetts 02114 —
University of Michigan/Kellogg Eye Center Ann Arbor Michigan 48105 —
The Retina Center Minneapolis Minnesota 55404 —
Retina Center of NJ, LLC. Bloomfield New Jersey 07003 —
Casey Eye Institute/Oregon Health & Science University Portland Oregon 97239 —
Wills Eye Hospital/Mid Atlantic Retina Philadelphia Pennsylvania 19107 —
UPMC Eye Center Pittsburgh Pennsylvania 15213 —
Palmetto Retina Center West Columbia South Carolina 29169 —
Austin Retina Associates Austin Texas 78705 —
Retina Foundation of the Southwest Dallas Texas 75231 —
Strategic Clinical Research Group Willow Park Texas 76087 —
University of Utah John A. Moran Eye Center Salt Lake City Utah 84132 —

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

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 24 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT03364153, 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 Apr 15, 2026 · 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 NCT03364153 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →