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 trial of GV101 for the treatment of cavernous malformations located in the brainstem

Trial Profile

A Phase 2 trial of GV101 for the treatment of cavernous malformations located in the brainstem

Status: Planning
Phase of Trial: Phase II

Latest Information Update: 18 Nov 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 GV 101 (Primary)
  • Indications Cavernous haemangioma
  • Focus Adverse reactions; Proof of concept

Most Recent Events

  • 12 Nov 2024 According to an Ovid Therapeutics media release, received regulatory clearance to initiate a Phase 2 program in Israel and were in the process of applying for clearance in other regions.
  • 12 Nov 2024 According to an Ovid Therapeutics media release, Ovid and Graviton are pausing the initiation of a Phase 2 study of OV888/GV101 to evaluate emerging insights from two recently completed competitor trials in cerebral cavernous malformations.
  • 13 Aug 2024 According to an Ovid Therapeutics media release, Ovid and Graviton Bioscience are on track to initiate a Phase 2 proof-of-concept program evaluating the safety and efficacy of OV888/GV101 in H2 2024.

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