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 Phase I, Multiple-dose study to access the Safety, tolerability and pharmacokinetics of Ombitasvir/paritaprevir/ritonavir and Dasabuvir in Healthy Han Chinese Subjects residing in USA

Trial Profile

A Phase I, Multiple-dose study to access the Safety, tolerability and pharmacokinetics of Ombitasvir/paritaprevir/ritonavir and Dasabuvir in Healthy Han Chinese Subjects residing in USA

Status: Completed
Phase of Trial: Phase I

Latest Information Update: 10 Jul 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

Most Recent Events

  • 10 Jul 2018 New trial record
  • 16 Jun 2018 Results assessing the Pharmacokinetics of Ombitasvir, Paritaprevir, Ritonavir, and Dasabuvir in Healthy and HCV GT1b-Infected Chinese, Korean and Taiwanese Patients from NCT02534870, NCT02517515, NCT02517528 and one more study, published in the European Journal of Drug Metabolism and Pharmacokinetics

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