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Completed Phase 2 Interventional Results available

Clinical Study to Investigate Safety and Efficacy of GSK933776 in Adult Patients With Geographic Atrophy Secondary to Age-related Macular Degeneration

ClinicalTrials.gov ID: NCT01342926

Public ClinicalTrials.gov record NCT01342926. 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 27, 2026, 11:28 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

A Phase 2, Multi-centre, Randomised, Double-masked, Placebo-controlled, Parallel-group Study to Investigate the Safety, Tolerability, Efficacy, Pharmacokinetics and Pharmacodynamics of GSK933776 in Adult Patients With Geographic Atrophy (GA) Secondary to Age-related Macular Degeneration (AMD)

Brief summary

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

The purpose of this study is to determine the safety and efficacy of GSK933776 in the treatment of geographic atrophy secondary to age-related macular degeneration.

Study identification

NCT ID
NCT01342926
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
GlaxoSmithKline
Industry
Enrollment
191 participants

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
55 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
Jun 1, 2011 (Type not available)
Primary completion
Apr 1, 2016 (Actual)
Completion
Apr 1, 2016 (Actual)
Last update posted
May 5, 2017

2011 – 2016

United States locations

U.S. sites
40
U.S. states
20
U.S. cities
37
Facility City State ZIP Site status
GSK Investigational Site Phoenix Arizona 85014 —
GSK Investigational Site Phoenix Arizona 85020 —
GSK Investigational Site Arcadia California 91007 —
GSK Investigational Site Irvine California 92697 —
GSK Investigational Site La Jolla California 92037 —
GSK Investigational Site Los Angeles California 90033-4500 —
GSK Investigational Site Palm Desert California 92260 —
GSK Investigational Site San Francisco California 94143 —
GSK Investigational Site Torrance California 90503 —
GSK Investigational Site Golden Colorado 80401 —
GSK Investigational Site Miami Florida 33136 —
GSK Investigational Site Stuart Florida 34994 —
GSK Investigational Site Tampa Florida 33612 —
GSK Investigational Site Augusta Georgia 30909 —
GSK Investigational Site Indianapolis Indiana 46290 —
GSK Investigational Site New Albany Indiana 47150 —
GSK Investigational Site Leawood Kansas 66211 —
GSK Investigational Site Prairie Village Kansas 66208 —
GSK Investigational Site Louisville Kentucky 40215 —
GSK Investigational Site Paducah Kentucky 42001 —
GSK Investigational Site Baltimore Maryland 21204 —
GSK Investigational Site Baltimore Maryland 21287 —
GSK Investigational Site Boston Massachusetts 02111 —
GSK Investigational Site North Dartmouth Massachusetts 02747 —
GSK Investigational Site Detroit Michigan 48202 —
GSK Investigational Site Northfield New Jersey 08225 —
GSK Investigational Site Toms River New Jersey 08755 —
GSK Investigational Site New York New York 10003 —
GSK Investigational Site Philadelphia Pennsylvania 19104 —
GSK Investigational Site Philadelphia Pennsylvania 19107 —
GSK Investigational Site West Mifflin Pennsylvania 15122 —
GSK Investigational Site Ladson South Carolina 29406 —
GSK Investigational Site Nashville Tennessee 37203 —
GSK Investigational Site Abilene Texas 79606 —
GSK Investigational Site Austin Texas 78705 —
GSK Investigational Site Galveston Texas 77550 —
GSK Investigational Site Houston Texas 77030 —
GSK Investigational Site Salt Lake City Utah 84132 —
GSK Investigational Site Charlottesville Virginia 22903 —
GSK Investigational Site Silverdale Washington 98383 —

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 1 non-U.S. site.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01342926, 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 5, 2017 · Synced Oct 27, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT01342926 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →