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 2, Randomized, Double-blind, Sham Surgery-controlled Study of the Efficacy and Safety of Intraputaminal AAV2-GDNF in the Treatment of Adults With Moderate Stage Parkinson's Disease

Next Previous
Trial Profile

A Phase 2, Randomized, Double-blind, Sham Surgery-controlled Study of the Efficacy and Safety of Intraputaminal AAV2-GDNF in the Treatment of Adults With Moderate Stage Parkinson's Disease

Status: Recruiting
Phase of Trial: Phase II

Latest Information Update: 03 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 AB 1005 (Primary)
  • Indications Parkinson's disease
  • Focus Therapeutic Use
  • Acronyms REGENERATE-PD
  • Sponsors Asklepios BioPharmaceutical

Most Recent Events

  • 14 Jan 2025 According to an Bayer media release, trial will be carried out across United States, Germany, Poland, and the United Kingdom.
  • 14 Jan 2025 According to an Bayer media release, Dr Rajesh Pahwa is the Principal Investigator of this trial.
  • 14 Jan 2025 According to an Bayer media release, first participants have been randomized.

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