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 pilot study to evaluate the safety, tolerability and efficacy of obeticholic acid (INT-747) for the treatment of portal hypertension

Trial Profile

A pilot study to evaluate the safety, tolerability and efficacy of obeticholic acid (INT-747) for the treatment of portal hypertension

Status: Completed
Phase of Trial: Phase II

Latest Information Update: 26 Mar 2018

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 Obeticholic acid (Primary)
  • Indications Portal hypertension
  • Focus Adverse reactions; Proof of concept; Therapeutic Use
  • Acronyms PESTO
  • Sponsors Intercept Pharmaceuticals

Most Recent Events

  • 23 Jan 2014 New trial record
  • 09 Jan 2014 Results of this trial have been submitted for presentation at the International Liver Congress of the European Association for the Study of the Liver (EASL) in April 2014, according to an Intercept Pharmaceuticals media release.
  • 09 Jan 2014 Results from this trial support the initiation of a double-blind phase IIB trial of obeticholic acid in the treatment of portal hypertension, according to an Intercept Pharmaceuticals media release.

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