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 Study of the Efficacy and Safety of QLT091001 in Subjects with Inherited Retinal Disease (IRD) Caused by Mutation in Retinal Pigment Epithelium Protein 65 (RPE65) or Lecithin:Retinol Acyltransferase (LRAT)

Trial Profile

A Study of the Efficacy and Safety of QLT091001 in Subjects with Inherited Retinal Disease (IRD) Caused by Mutation in Retinal Pigment Epithelium Protein 65 (RPE65) or Lecithin:Retinol Acyltransferase (LRAT)

Status: Recruiting
Phase of Trial: Phase III

Latest Information Update: 19 Feb 2021

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 Zuretinol acetate (Primary)
  • Indications Leber congenital amaurosis; Retinitis pigmentosa
  • Focus Registrational; Therapeutic Use
  • Sponsors Novelion Therapeutics

Most Recent Events

  • 19 Feb 2021 This trial is discontinued in Denmark, according to European Clinical Trials Database record.
  • 10 Dec 2016 Status changed from planning to recruiting.
  • 01 Nov 2016 According to a QLT media release, the company is planning to initiate this trial in the fourth quarter of 2016.

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