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Clinical Trial Summary

Phase 1 open-label study to assess the bioactivity, ocular and systemic safety, tolerability, and pharmacokinetics of a single dose injections of EYP-1901 at three dose levels: 440 µg, 2060 µg and 3090 µg in subjects with Wet Age Related Macular Degeneration (wAMD)


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04747197
Study type Interventional
Source EyePoint Pharmaceuticals, Inc.
Contact
Status Completed
Phase Phase 1
Start date January 20, 2021
Completion date May 11, 2022

See also
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Completed NCT03585556 - AAVCAGsCD59 for the Treatment of Wet AMD Phase 1
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Terminated NCT01086761 - Study of MP0112 Intravitreal Injection in Patients With Wet Age Related Macular Degeneration Phase 1
Recruiting NCT05727397 - Efficacy and Safety of RC28-E Versus Aflibercept Phase 3
Completed NCT04884399 - Phase I Study to Compare CMAB818 Injection and Lucentis® in Patients With Wet AMD Phase 1
Completed NCT04964089 - A Study to Evaluate the Efficacy and Safety of Intravitreal KSI-301 Compared With Intravitreal Aflibercept in Participants With Neovascular (Wet) Age-related Macular Degeneration (wAMD) Phase 3
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