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 Randomized, Double-blind Study to Compare the Effect of up to 100 Days, and up to 200 Days, of Treatment With Valcyte (Valganciclovir) on Prevention of Cytomegalovirus Disease in High-risk Kidney Allograft Recipients.

Next Previous
X
Search
Trial Profile

A Randomized, Double-blind Study to Compare the Effect of up to 100 Days, and up to 200 Days, of Treatment With Valcyte (Valganciclovir) on Prevention of Cytomegalovirus Disease in High-risk Kidney Allograft Recipients.

Status: Completed
Phase of Trial: Phase III

Latest Information Update: 05 Oct 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 Valganciclovir (Primary)
  • Indications Cytomegalic inclusion disorders
  • Focus Registrational; Therapeutic Use
  • Acronyms IMPACT
  • Sponsors Roche

    • Most Recent Events

    • 01 Mar 2012 Results of the ganciclovir resistance analysis published in the Journal of Clinical Virology.
    • 27 Dec 2010 Two-year results published in Transplantation.
    • 19 Aug 2010 Results reported at 23rd International Congress of the Transplantation Society.

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