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Evaluation of the Safety and Tolerability of OLX10212 in Patients With Neovascular Age-Related Macular Degeneration

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Trial Profile

Evaluation of the Safety and Tolerability of OLX10212 in Patients With Neovascular Age-Related Macular Degeneration

Status: Recruiting
Phase of Trial: Phase I

Latest Information Update: 23 Feb 2024

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At a glance

  • Drugs OLX 301A (Primary)
  • Indications Age-related macular degeneration
  • Focus First in man; Therapeutic Use
  • Sponsors OliX Pharmaceuticals

    • Most Recent Events

    • 10 Jan 2024 Planned number of patients changed from 48 to 42.
    • 29 Nov 2023 preliminary Results (n=15) presented in the OliX Pharmaceuticals Media Release.
    • 21 Sep 2023 Protocol amended to change dose in part A 1178.8 to 895.9 micro g/eye. Patient number changed.

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