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 Two-Part, Single-Centre, Open (Part A) Single Blind (Part B), Randomised, Placebo-Controlled Phase I Study to Assess the Safety, Tolerability and Pharmacokinetics After Single Doses With and Without Food and Multiple Ascending Oral Doses of AZD1305 Extended-Release Tablet in Healthy and Elderly Subjects.

Trial Profile

A Two-Part, Single-Centre, Open (Part A) Single Blind (Part B), Randomised, Placebo-Controlled Phase I Study to Assess the Safety, Tolerability and Pharmacokinetics After Single Doses With and Without Food and Multiple Ascending Oral Doses of AZD1305 Extended-Release Tablet in Healthy and Elderly Subjects.

Status: Completed
Phase of Trial: Phase I

Latest Information Update: 09 Jun 2021

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 AZD 1305 (Primary)
  • Indications Arrhythmias
  • Focus Adverse reactions

Most Recent Events

  • 02 Dec 2010 Actual end date changed from Aug 2008 to Jul 2008 as reported by ClinicalTrials.gov.
  • 17 Aug 2008 Status changed from active, no longer recruiting to completed as reported by ClinicalTrials.gov.
  • 25 Jun 2008 New trial record.

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