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Regulatory Post-Marketing Surveillance Study for Brolucizumab

Recruitingn/aAges 18 Years - 100 YearsAllNovartis Pharmaceuticals
NCT04985487 on ClinicalTrials.gov ↗
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In plain words

What the trial is, and whether it could suit you

This study is an open-label, multicenter, single-arm, observational post-marketing surveillance.

Sign in to get the eligibility rules as simple questions to take to your doctor.

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📋 Eligibility rules (as published)
Inclusion Criteria: 1. Patients aged ≥18 years with nAMD that are prescribed with Brolucizumab as per approved local product information 2. Patients who consent to participate in the study after the purpose and nature of the study have clearly explained to them (written informed consent) Exclusion Criteria: 1. Contraindications as per local prescribing information 1) Hypersensitivity to the active substance or to any of the excipients. 2) Active or suspected ocular or periocular infection. 3) Active intraocular inflammation. 2. Patients participating in other investigational drug trial
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What it tests

  • brolucizumab
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Where

28 sites
Novartis Investigative Site
Daegu, South Korea
Novartis Investigative Site
Goyang-si, South Korea
Novartis Investigative Site
Guri-si, South Korea
Novartis Investigative Site
Suwon, South Korea
Novartis Investigative Site
Iksan Si, South Korea
Novartis Investigative Site
Daejeon, South Korea
Novartis Investigative Site
Busan, South Korea
Novartis Investigative Site
Busan, South Korea

…and 20 more on ClinicalTrials.gov.

🤝 Taking part is your choice, and you can leave at any time. Only the trial team can confirm you are eligible — always decide together with your own doctor.
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