Overview

Efficacy and Safety of AL-001 Ophthalmic Injection in Subjects with WAMD

Status:
NOT_YET_RECRUITING
Trial end date:
2027-01-30
Target enrollment:
Participant gender:
Summary
This Phase II study is designed to evaluate the efficacy and safety of AL-001 ophthalmic injection in patients with wet age-related macular degeneration. Eligible patients, who meet the inclusion/exclusion criteria and have shown an anatomic response to an anti-VEGF (Vascular Endothelial Growth Factor) injection, will be randomized in Cohorts 1 and 2 to receive AL-001 administered via suprachoroidal space injection, Cohort 3 to receive Aflibercept.
Phase:
PHASE2
Details
Lead Sponsor:
Beijing Anlong Biopharmaceutical Co., Ltd.
Treatments:
aflibercept