This Phase I/IIa study is designed to evaluate the safety, tolerability, preliminary pharmacodynamics and pharmacokinetics 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 receive a single dose of AL-001 administered via suprachoroidal space injection.
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
21
Administered via suprachoroidal space injection.
Chinese Academy of Medical Sciences & Peking Union Hospital
Beijing, China
Safety and tolerability
Incidence of adverse events (AEs) and serious adverse events (SAEs)
Time frame: Week 24
Evaluate the effect of AL-001 on BCVA
Mean change from baseline in BCVA
Time frame: Week 52
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