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 study comparing rivaroxaban or warfarin versus low molecular weight heparin (LMWH) for the treatment of venous-thromboembolism in cancer patients

Next Previous
X
Search
Trial Profile

A study comparing rivaroxaban or warfarin versus low molecular weight heparin (LMWH) for the treatment of venous-thromboembolism in cancer patients

Status: Completed
Phase of Trial: Phase II

Latest Information Update: 19 Feb 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 Rivaroxaban (Primary) ; Warfarin (Primary)
  • Indications Venous thromboembolism
  • Focus Therapeutic Use
  • Sponsors Janssen; Johnson & Johnson Innovative Medicine

    • Most Recent Events

    • 18 Dec 2015 New trial record
    • 07 Dec 2015 According to a Janssen Pharmaceuticals media release, results from this trial were presented at the 2015 American Society of Hematology (ASH) Annual Meeting.
    • 07 Dec 2015 Results were published in a Janssen Pharmaceuticals media release.

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