Trial Profile

A Multicenter, Dose-escalation and Dose-expansion, Phase I/II Clinical Study to Evaluate the Safety, Tolerability, Pharmacokinetics and Efficacy Characteristics of SCT520FF in Patients With Neovascular Age-related Macular Degeneration

Status: Recruiting

Phase of Trial: Phase I/II

Latest Information Update: 06 Oct 2025

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At a glance

04 Sep 2025 Protocol has been amended to include one new arm (Active Comparator: eylea 2 mg) , it has been changed 3 to 4 .
04 Sep 2025 Planned number of patients changed from 15 to 82.
04 Sep 2025 Status changed from not yet recruiting to recruiting.

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