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 two-part study to evaluate the safety, tolerability, and pharmacokinetics of single and repeat oral doses of GSK557296 in a randomized, single-blind, placebo-controlled, dose-rising design, and to evaluate the effect of food on single oral doses of GSK557296 in healthy adult subjects.

X
Trial Profile

A two-part study to evaluate the safety, tolerability, and pharmacokinetics of single and repeat oral doses of GSK557296 in a randomized, single-blind, placebo-controlled, dose-rising design, and to evaluate the effect of food on single oral doses of GSK557296 in healthy adult subjects.

Status: Completed
Phase of Trial: Phase I

Latest Information Update: 20 Aug 2023

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 Epelsiban (Primary)
  • Indications Premature ejaculation
  • Focus Adverse reactions
  • Sponsors GlaxoSmithKline; GSK
  • Most Recent Events

    • 12 Oct 2008 Status changed from not yet recruiting to completed as reported by ClinicalTrials.gov.
    • 07 Nov 2007 New trial record.

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