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 Randomized, Double-Blind, Placebo-Controlled, Analytically Masked Sequential-Panel, Ascending Single-Dose, and Repeated Twice Daily-Dose Study to Evaluate the Safety, Tolerability, Pharmacokinetics and Analgesic Efficacy of Oral CMX-020 in Healthy Male and Female Subjects.

Next Previous
Search
Trial Profile

A Randomized, Double-Blind, Placebo-Controlled, Analytically Masked Sequential-Panel, Ascending Single-Dose, and Repeated Twice Daily-Dose Study to Evaluate the Safety, Tolerability, Pharmacokinetics and Analgesic Efficacy of Oral CMX-020 in Healthy Male and Female Subjects.

Status: Completed
Phase of Trial: Phase I

Latest Information Update: 16 Jul 2019

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 CMX 020 (Primary)
  • Indications Neuropathic pain; Postoperative pain
  • Focus Adverse reactions

Most Recent Events

  • 07 Aug 2015 Status changed from active, no longer recruiting to completed, as reported by Australian New Zealand Clinical Trials Registry
  • 04 Jun 2015 Status changed from recruiting to active, no longer recruiting as per Australian New Zealand Clinical Trials Registry.
  • 17 Apr 2015 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