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?

Twelve-months Extension Study to Explore the Long-Term Safety and Efficacy of Subcutaneous Administration of GV1001 1.12 Mg/day in Patients with Progressive Supranuclear Palsy Who Completed Study GV1001-PSP-CL2-011

Trial Profile

Twelve-months Extension Study to Explore the Long-Term Safety and Efficacy of Subcutaneous Administration of GV1001 1.12 Mg/day in Patients with Progressive Supranuclear Palsy Who Completed Study GV1001-PSP-CL2-011

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

Latest Information Update: 25 Oct 2024

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 Tertomotide (Primary)
  • Indications Progressive supranuclear palsy
  • Focus Adverse reactions
  • Sponsors GemVax & KAEL
  • Most Recent Events

    • 23 Oct 2024 Planned End Date changed from 30 Jul 2025 to 1 Dec 2025.
    • 23 Oct 2024 Planned primary completion date changed from 15 Dec 2024 to 1 Nov 2025.
    • 23 Oct 2024 Status changed from recruiting to active, no longer recruiting.

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

If your organization or you do not have a subscription, try one of the following:
  • Contacting your organization’s admin about adding this content to your AdisInsight subscription
  • Buying a PDF version of any individual profile
  • Request a free trial
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