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A Phase II, Multicenter, Randomized, Single-Masked, Sham Injection-Controlled Exposure-Response Study of Lampalizumab Intravitreal Injections Administered Every Two Weeks or Every Four Weeks to Patients With Geographic Atrophy
This multicenter, randomized, single-masked, sham injection-controlled study will investigate the exposure-response and safety of lampalizumab administered intravitreally every 2 weeks (Q2W) or every 4 weeks (Q4W) for 24 weeks in participants with geographic atrophy (GA) secondary to age-related macular degeneration (AMD). A safety run-in assessment will be conducted prior to initiating enrollment in the randomized study.
Age
60 - No limit years
Sex
ALL
Healthy Volunteers
No
Barnet Dulaney Perkins Eye Center
Mesa, Arizona, United States
University of Arizona; Banner University Medical, Department of Opthalmology
Tucson, Arizona, United States
Northwest Arkansas Retina Associates
Springdale, Arkansas, United States
Retinal Diagnostic Center
Campbell, California, United States
The Retina Partners
Encino, California, United States
Loma Linda University
Loma Linda, California, United States
San Diego Retina Associates
Oceanside, California, United States
West Coast Retina Medical Group
San Francisco, California, United States
California Retina Consultants
Santa Barbara, California, United States
Colorado Retina Associates, PC
Golden, Colorado, United States
Start Date
March 30, 2015
Primary Completion Date
June 2, 2017
Completion Date
June 2, 2017
Last Updated
September 25, 2019
96
ACTUAL participants
Sham
OTHER
Lampalizumab
DRUG
Lead Sponsor
Genentech, Inc.
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