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?

Study comparing the effectiveness of Selexipag versus subcutaneous Treprostinil versus intravenous Epoprostenol in treating Pulmonary Arterial Hypertension

Trial Profile

Study comparing the effectiveness of Selexipag versus subcutaneous Treprostinil versus intravenous Epoprostenol in treating Pulmonary Arterial Hypertension

Status: Completed
Phase of Trial: Phase IV

Latest Information Update: 02 Nov 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 Selexipag (Primary) ; Epoprostenol; Treprostinil
  • Indications Pulmonary arterial hypertension
  • Focus Therapeutic Use

Most Recent Events

  • 24 May 2020 New trial record
  • 20 May 2020 Results comparing the effects of Selexipag (S) vs subcutaneous Treprostinil (T) vs intravenous Epoprostenol (E) in PAH patients who initially started with double-combination therapy with endothelin receptor antagonist (ERA) and phosphodiesterase-5 inhibitor (PDE5-I), presented at the 116th International Conference of the American Thoracic Society.
  • 30 Mar 2020 Results presented at the 2020 Annual Scientific Session of the American College of Cardiology and World Congress of Cardiology

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