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Open-label, Multiple Dose, Dose Escalation Study to Evaluate the Safety/Tolerability and Efficacy of EA-2353 in Subjects With Retinitis Pigmentosa

Trial Profile

Open-label, Multiple Dose, Dose Escalation Study to Evaluate the Safety/Tolerability and Efficacy of EA-2353 in Subjects With Retinitis Pigmentosa

Status: Discontinued
Phase of Trial: Phase I/II

Latest Information Update: 21 Oct 2024

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At a glance

  • Drugs EA-2353 (Primary)
  • Indications Retinitis pigmentosa
  • Focus Adverse reactions
  • Sponsors Endogena Therapeutics

Most Recent Events

  • 14 Oct 2024 Status changed from active, no longer recruiting to discontinued.
  • 04 May 2023 According to an Endogena Therapeutics media release, the first patient started treatment in July 2022 and topline interim data is anticipated in early 2024.
  • 04 May 2023 According to an Endogena Therapeutics media release, company announced that it has completed patient enrollment ahead of schedule in this trial, with the dose-escalation stage completed in April, the ongoing trial is now in the expansion cohort stage.The trial is being conducted across five US sites.

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