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, single-blind, two-way, parallel, single-site, repeat-dose study evaluating effect of IV morphine on the intestinal absorption of orally administered acetaminophen in healthy subjects.

Next Previous
X
Search
Trial Profile

A randomized, single-blind, two-way, parallel, single-site, repeat-dose study evaluating effect of IV morphine on the intestinal absorption of orally administered acetaminophen in healthy subjects.

Status: Completed
Phase of Trial: Phase I

Latest Information Update: 01 Dec 2016

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 Morphine (Primary) ; Paracetamol (Primary) ; Paracetamol (Primary)
  • Indications Pain
  • Focus Pharmacokinetics

    • Most Recent Events

    • 01 Dec 2016 New trial record
    • 18 Nov 2016 According to a Mallinckrodt Inc.media release, results will be presented at the 15th Annual Pain Medicine Meeting of the American Society of Regional Anesthesiology and Pain Medicine (ASRA)
    • 18 Nov 2016 Results published in the Mallinckrodt Inc. 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