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Not yet recruiting Phase 2 Interventional

A Study in Adults With Geographic Atrophy

ClinicalTrials.gov ID: NCT07606365

Public ClinicalTrials.gov record NCT07606365. 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 Sep 3, 2026, 9:32 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, Multicentre, Randomised, Double-masked, Placebo-controlled, Parallel-group, Dose-range Finding Study, to Assess the Efficacy and Safety of Oral STL303 in Adults With Geographic Atrophy Secondary to Age-related Macular Degeneration

Brief summary

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

The purpose of this clinical research study is to look at how safe STL303 is and whether it works when given to people with Geographic Atrophy (GA) secondary to Age-related Macular Degeneration (AMD). Geographic atrophy secondary to AMD is a condition where cells in the back part of the eye slowly die, causing a blurry, or missing spot in the centre of vision.

Study identification

NCT ID
NCT07606365
Recruitment status
Not yet recruiting
Study type
Interventional
Phase
Phase 2
Lead sponsor
Sitala Bio LTD
Industry
Enrollment
300 participants

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
60 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
May 31, 2026
Primary completion
Jun 30, 2028
Completion
Jul 31, 2029
Last update posted
May 27, 2026

2026 – 2029

United States locations

U.S. sites
20
U.S. states
13
U.S. cities
19
Facility City State ZIP Site status
California Retina Consultants Bakersfield California 93309
Retina-Vitreous Associates Medical Group Beverly Hills California 90211
Kaiser Permanente - Oakland Oakland California 94612
Retina Specialists of Colorado Aurora Colorado 80012
Retina Group of New England, PC Waterford Connecticut 06385
Retina Vitreous Associates of Florida St. Petersburg Florida 33711
Florida Retina Institute Wildwood Florida 34785
University Retina and Macula Associates, P.C. Lemont Illinois 60439
Associated Vitreoretinal and Uveitis Consultants Carmel Indiana 46032
Cumberland Valley Retina Consultants,P.C. Hagerstown Maryland 21740
Mid Atlantic Retina Specialists Hagerstown Maryland 21740
Ophthalmic Consultants of Boston Waltham Massachusetts 02451
Long Island and Queens Vitreoretinal Consultants of NY, P.C. Hauppauge New York 11788
Erie Retina Research Erie Pennsylvania 16507
Tennessee Retina, PC Nashville Tennessee 37203
Retina Consultants of Texas Bellaire Texas 77401
Star Vision Research Burleson Texas 76028
Retina Consultants of Texas Schertz Texas 78154
Northeast Wisconsin Retina Associates Appleton Wisconsin 54914
Eye Clinic of Wisconsin Wausau Wisconsin 54403

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 40 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT07606365, 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 May 27, 2026 · Synced Sep 3, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT07606365 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →