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The purpose of the extension study was to provide patients completing the 28-week core study (NCT01095250) with an opportunity to receive an additional 22 weeks of continuous treatment.
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Lead Sponsor
Novartis
NCT07552012 · Active Non-anterior, Non-infectious Uveitis
NCT07218770 · Active Noninfectious Uveitis Affecting the Posterior Segment
NCT06974162 · Uveitis, Aqueous Humor, and more
NCT07145008 · Macular Edema (ME), Non Infectious Uveitis
NCT05486468 · Uveitis, Uveitis, Posterior, and more
Texas Retina Associates
Arlington, Texas
Novartis Investigative Site
London, Ontario
Novartis Investigative Site
North York, Ontario
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Start free trial →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.
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