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?

Phase II efficacy and safety of Taro pharmaceuticals' pro-drug T2000 (1,3-dimethoxymethyl-5,5-diphenyl-barbituric acid) in patients with myoclonus dystonia: an open label sequential dose escalation study

Next Previous
X
Search
Trial Profile

Phase II efficacy and safety of Taro pharmaceuticals' pro-drug T2000 (1,3-dimethoxymethyl-5,5-diphenyl-barbituric acid) in patients with myoclonus dystonia: an open label sequential dose escalation study

Status: Discontinued
Phase of Trial: Phase II

Latest Information Update: 26 Dec 2013

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 T 2000 (Primary)
  • Indications Dystonia
  • Focus Therapeutic Use
  • Sponsors Taro Pharmaceuticals USA

    • Most Recent Events

    • 25 Oct 2011 Planned end date changed from 1 Sep 2011 to 1 Oct 2011 as reported by ClinicalTrials.gov.
    • 25 Oct 2011 Status changed from recruiting to discontinued as reported by ClinicalTrials.gov.
    • 26 Nov 2010 Planned End Date changed from 1 Mar 2011 to 1 Sep 2011.

You need to be a logged in or subscribed to view this content Request demo

If your organization or you do not have a subscription, try one of the following:
  • Contacting your organization’s admin about adding this content to your AdisInsight subscription
  • Buying a PDF version of any individual profile
  • Request a free trial
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