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A Long-term Follow-up Study to Evaluate the Safety and Effectivity of AL-001 Ophthalmic Injection in Subjects with Wet Age-related Mecular Degeneration (wAMD)
This study is designed to evaluate long-term safety and efficacy of AL-001 ophthalmic injection following suprachoroidal space(SCS) administration in subjects with wAMD. Eligible patients, are those who were previously enrolled in a clinical study in which they received a single dose of AL-001 administered via suprachoroidal space injection.
Age
50 - No limit years
Sex
ALL
Healthy Volunteers
No
Chinese Academy of Medical Sciences & Peking Union Hospital
Beijing, Beijing Municipality, China
Start Date
December 9, 2024
Primary Completion Date
June 30, 2029
Completion Date
June 30, 2029
Last Updated
December 5, 2024
21
ESTIMATED participants
Lead Sponsor
Beijing Anlong Biopharmaceutical Co., Ltd.
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.
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