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?

Phase II, multicentric, prospective and opened clinical trial of advanced valganciclovir treatment of CMV in allogenic hematopoietic progenitors transplant

X
Trial Profile

Phase II, multicentric, prospective and opened clinical trial of advanced valganciclovir treatment of CMV in allogenic hematopoietic progenitors transplant

Status: Completed
Phase of Trial: Phase II

Latest Information Update: 01 Jun 2011

Price : $35 *
  • 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 Cytomegalovirus infections
  • Focus Therapeutic Use
  • Most Recent Events

    • 22 Sep 2009 Actual end date (1 Sep 2009) added as reported by ClinicalTrials.gov.
    • 22 Sep 2009 Status changed from active, no longer recruiting to completed ass reported by ClinicalTrials.gov
    • 20 May 2009 Status changed from recruiting to active, no longer recruiting as reported by ClinicalTrials.gov.

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