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?

Real World Study Comparing Incidence of Thromboembolic Events in Patients of Polycythemia Vera Treated with Hydroxyurea (HU) and Switched to Ruxolitinib

Trial Profile

Real World Study Comparing Incidence of Thromboembolic Events in Patients of Polycythemia Vera Treated with Hydroxyurea (HU) and Switched to Ruxolitinib

Status: Completed
Phase of Trial: Phase IV

Latest Information Update: 22 Jul 2020

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 Ruxolitinib (Primary) ; Hydroxycarbamide
  • Indications Polycythaemia vera
  • Focus Adverse reactions

Most Recent Events

  • 21 Jun 2020 Results presented at the 25th Congress of the European Haematology Association
  • 05 Dec 2019 New trial record
  • 06 Nov 2019 Results, comparing the incidence of Thromboembolic events in hydroxyurea -treated polycythemia vera patients who switched to ruxolitinib after initial treatment hydroxyurea or continued hydroxyurea without switching with the help of OPTUM database, released at the 61st Annual Meeting and Exposition of the American Society of Hematology

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