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, Multicenter, Double-Blind Comparison of LY2140023 and Aripiprazole in Patients With DSM-IV-TR Schizophrenia Followed by Open-Label Treatment With LY2140023.

Trial Profile

A Phase 3, Multicenter, Double-Blind Comparison of LY2140023 and Aripiprazole in Patients With DSM-IV-TR Schizophrenia Followed by Open-Label Treatment With LY2140023.

Status: Discontinued
Phase of Trial: Phase III

Latest Information Update: 09 Sep 2022

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 Pomaglumetad methionil (Primary) ; Aripiprazole
  • Indications Schizophrenia
  • Focus Pharmacodynamics; Registrational
  • Sponsors Denovo Biopharma; Eli Lilly and Company

Most Recent Events

  • 05 Oct 2021 this study has been completed in Spain ( global end of the trial 2012-10-12 ) as per European Clinical Trials Database record
  • 29 Aug 2012 Status changed from active, no longer recruiting to discontinued, according to an Eli Lilly media release.
  • 15 May 2012 Planned end date changed from 1 Apr 2013 to 1 May 2013 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