AL-001 Injection for Wet Age-related Macular Degeneration

Long-term Follow-up Study of AL-001 Ophthalmic Injection in Subjects with WAMD

Recruiting Observational Study
Wet Age-related Macular Degeneration (wAMD)
No Placebo Group Every participant receives an active treatment — no one gets a placebo. No Study Drug Researchers observe your health over time — no experimental treatment is given.
Ready to participate?

Review the details below, then apply to join this clinical trial.

At a Glance
Age
50 and older
Sex
Any
Study type
Observational
Participants needed
21 (estimated)
Sponsor
Beijing Anlong Biopharmaceutical Co., Ltd. · Industry
Who this trial is looking for

This trial is looking for patients who have previously received the AL-001 injection for wet age-related macular degeneration. Participants will help evaluate the long-term safety and effectiveness of this treatment.

Are You a Good Fit for This Trial?

You may be able to join if

  • I have received the AL-001 ophthalmic injection in a previous study.
  • I agree to participate and sign a written consent form.
  • I am willing and able to attend scheduled visits and follow procedures.

Summarized in plain language from this trial's official eligibility criteria. The full criteria are further down this page — only the research team can confirm whether you qualify.

Think this trial could be right for you?

Answer a few quick questions to see if you may meet the eligibility requirements.

Check Your Eligibility
About This Trial

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.

Trial Locations
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Eligibility Criteria
Inclusion Criteria: * The subjects enrolled in AL-001 study and received AL-001 ophthalmic injection. * The subject or their legal representative agrees to participate in this study and signs a written ICF. * The subjects are willing and able to follow planned visits and procedures. Exclusion Crit…
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