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Completed Phase 2 Interventional

Study of the Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of ACU-4429 in Subjects With Geographic Atrophy

ClinicalTrials.gov ID: NCT01002950

Public ClinicalTrials.gov record NCT01002950. 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 1, 2026, 10:21 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

Multicenter, Randomized, Double-Masked, Placebo-Controlled, Dose Escalation, Multiple-Dose Study of the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of ACU-4429 in Subjects With Dry Age-Related Macular Degeneration (Geographic Atrophy)

Brief summary

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

The purpose of this study is to evaluate the safety, tolerability, pharmacokinetics and pharmacodynamics of the investigational drug ACU-4429 in subjects with geographic atrophy.

Study identification

NCT ID
NCT01002950
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Kubota Vision Inc.
Industry
Enrollment
72 participants

Conditions and interventions

Eligibility (public fields only)

Age range
Not listed
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 30, 2009
Primary completion
May 31, 2012
Completion
Sep 30, 2012
Last update posted
Mar 10, 2014

2009 – 2012

United States locations

U.S. sites
12
U.S. states
9
U.S. cities
12
Facility City State ZIP Site status
Retinal Consultants of Arizona Phoenix Arizona 85014
Retina-Vitreous Associates Medical Group Beverly Hills California 90211
Covance Clinical Research Unit, Inc. Daytona Beach Florida 32117
National Ophthalmic Research Institute Fort Meyers Florida 33912
Covance Clinical Research Unit, Inc. Honolulu Hawaii 96813
Kresege Eye Institute Detroit Michigan 48201
Associated Retinal Consultants, P.C. / William Beaumont Hospital Royal Oak Michigan 48073
New York Eye and Ear Infirmary New York New York 10003
Cleveland Clinic Cleveland Ohio 44195
Black Hills Regional Eye Institute Rapid City South Dakota 57701
Covance Clinical Research Unit Austin Texas 78752
Covance Clinical Research Unit, Inc. Dallas Texas 75247

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 NCT01002950, 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 Mar 10, 2014 · Synced Sep 1, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01002950 live on ClinicalTrials.gov.

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