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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)
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.
Age
All ages
Sex
ALL
Healthy Volunteers
No
Retinal Consultants of Arizona
Phoenix, Arizona, United States
Retina-Vitreous Associates Medical Group
Beverly Hills, California, United States
Covance Clinical Research Unit, Inc.
Daytona Beach, Florida, United States
National Ophthalmic Research Institute
Fort Meyers, Florida, United States
Covance Clinical Research Unit, Inc.
Honolulu, Hawaii, United States
Kresege Eye Institute
Detroit, Michigan, United States
Associated Retinal Consultants, P.C. / William Beaumont Hospital
Royal Oak, Michigan, United States
New York Eye and Ear Infirmary
New York, New York, United States
Cleveland Clinic
Cleveland, Ohio, United States
Black Hills Regional Eye Institute
Rapid City, South Dakota, United States
Start Date
October 1, 2009
Primary Completion Date
June 1, 2012
Completion Date
October 1, 2012
Last Updated
March 11, 2014
72
ACTUAL participants
ACU-4429
DRUG
Matching placebo
DRUG
Lead Sponsor
Kubota Vision Inc.
Collaborators
NCT06779773
NCT06990269
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.
View ClinicalTrials.gov Terms and ConditionsNCT06970665