Either you have JavaScript disabled or your browser does not support Javascript . To work properly, this page requires JavaScript to be enabled.
How to enable JavaScript in your browser?

A Phase 2a Study to Evaluate Safety and Tolerability After Single Administration of PER-001 Intravitreal Implant in Participants With Diabetic Retinopathy

Trial Profile

A Phase 2a Study to Evaluate Safety and Tolerability After Single Administration of PER-001 Intravitreal Implant in Participants With Diabetic Retinopathy

Status: Active, no longer recruiting
Phase of Trial: Phase II

Latest Information Update: 01 Jul 2025

Price :
$35 *
Note:
  • Adis is an information provider.
  • Final gross price and currency may vary according to local VAT and billing address.
  • Your purchase entitles you to full access to the information contained in our trial profile at the time of purchase.
  • A link to download a PDF version of the trial profile will be included in your email receipt.

At a glance

  • Drugs PER 001 (Primary)
  • Indications Diabetic retinopathy
  • Focus Adverse reactions; Therapeutic Use
  • Sponsors Perfuse Therapeutics

Most Recent Events

  • 24 Jun 2025 According to a Perfuse Therapeutics media release, data from this study was presented at Clinical Trials at the Summit (CTS) meeting on June 21.
  • 24 Jun 2025 The 24-week data presented in the Perfuse Therapeutics Media Release.
  • 15 Apr 2025 Planned End Date changed from 31 May 2026 to 1 Apr 2026.

You need to be a logged in or subscribed to view this content

Request demo (opens in a new window)
If your organization or you do not have a subscription, try one of the following: If your organization has a subscription, there are several access options, even while working remotely:
  • Working within your organization’s network
  • with username/password or try to via your institution
  • Persisted access using your organization’s identifier stored in your user browser for 90 days
Back to top