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 II, double-blind, randomized, placebo-controlled non-inferiority trial of EpiCept NP-1 topical cream (2% ketamine / 4% amitriptyline) vs. oral gabapentin in postherpetic neuralgia

Next Previous
X
Search
Trial Profile

A phase II, double-blind, randomized, placebo-controlled non-inferiority trial of EpiCept NP-1 topical cream (2% ketamine / 4% amitriptyline) vs. oral gabapentin in postherpetic neuralgia

Status: Completed
Phase of Trial: Phase II

Latest Information Update: 30 Jul 2011

Price : $35 *
  • 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 Amitriptyline/ketamine (Primary) ; Gabapentin
  • Indications Neuropathic pain; Postherpetic neuralgia
  • Focus Registrational; Therapeutic Use

    • Most Recent Events

    • 15 Sep 2009 Actual end date (1 Jun 2009) added as reported by ClinicalTrials.gov
    • 15 Sep 2009 Status changed from active, no longer recruiting to completed as reported by ClinicalTrials.gov
    • 27 Jan 2009 Results are reported in a EpiCept Corporation media release.

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