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 3, Multicentre, Randomised, Investigator-Blinded, Parallel-group Study of the Safety and Efficacy of Intravenous Daptomycin (Cubicin) Compared With That of Comparator (Vancomycin or Vancomycin Followed by Semi-Synthetic Penicillin-Cloxacillin) in the Treatment of Chinese Subjects With cSSSI.

Next Previous
Trial Profile

A Phase 3, Multicentre, Randomised, Investigator-Blinded, Parallel-group Study of the Safety and Efficacy of Intravenous Daptomycin (Cubicin) Compared With That of Comparator (Vancomycin or Vancomycin Followed by Semi-Synthetic Penicillin-Cloxacillin) in the Treatment of Chinese Subjects With cSSSI.

Status: Completed
Phase of Trial: Phase III

Latest Information Update: 09 Nov 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 Daptomycin (Primary) ; Cloxacillin; Vancomycin
  • Indications Gram-positive infections; Skin and soft tissue infections
  • Focus Adverse reactions; Registrational
  • Sponsors AstraZeneca

Most Recent Events

  • 10 Sep 2010 Actual end date added to 1 Sep 2010 as reported by ClinicalTrials.gov.
  • 10 Sep 2010 Status changed from active, no longer recruiting to completed as reported by ClinicalTrials.gov.
  • 09 Aug 2010 Status changed from recruiting to active, no longer recruiting as reported by ClinicalTrials.gov.

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