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Clinical Trial Summary

Study ML43000 is a Phase IIIb/IV multicenter, open-label (visual assessor-masked) study designed to assess the efficacy and safety of PDS 100 mg/mL Q24W in patients with nAMD who have been previously treated with anti-VEGF agents other than ranibizumab. Approximately 200 patients will be enrolled at approximately 40 sites.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04853251
Study type Interventional
Source Genentech, Inc.
Contact Reference Study ID Number: ML43000 www.roche.com/about_roche/roc
Phone 888-662-6728 (U.S.)
Email [email protected]
Status Not yet recruiting
Phase Phase 3
Start date July 27, 2021
Completion date August 21, 2023

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