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Clinical Trial Summary

Multi-center, open-label, two-part safety assessment following administration of single ascending doses and repeat administration of the HTD of OCU-10-C-110 for Injection in the study eye of participants with nAMD


Clinical Trial Description

In Part A, subjects will receive a single intravitreal dose in a single eye of the drug product. Dose will be escalated in 3 successive cohorts, pending safety. In Part B, subjects will receive 3 treatments in a single eye of drug product at 4 week intervals of the maximally tolerated dose, with an additional 4 weeks of observation for safety. . ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05904691
Study type Interventional
Source Ocugenix Corporation
Contact Sean McDonald
Phone (412) 600-6379
Email sean@ocugenixtx.com
Status Recruiting
Phase Phase 1
Start date November 1, 2023
Completion date May 1, 2025

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