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, two-way crossover study to investigate the bioavailability of a single oral dose of 12.5 mg carbidopa, 50 mg levodopa and 200 mg entacapone compared to a single oral combined dose of both 12.5 mg carbidopa and 50 mg levodopa and 200 mg entacapone in healthy volunteers under fed conditions

Next Previous
X
Search
Trial Profile

A randomized, two-way crossover study to investigate the bioavailability of a single oral dose of 12.5 mg carbidopa, 50 mg levodopa and 200 mg entacapone compared to a single oral combined dose of both 12.5 mg carbidopa and 50 mg levodopa and 200 mg entacapone in healthy volunteers under fed conditions

Status: Completed
Phase of Trial: Phase I

Latest Information Update: 30 Mar 2007

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 Levodopa/carbidopa/entacapone (Primary) ; Entacapone; Levodopa/carbidopa
  • Indications Parkinson's disease
  • Focus Pharmacokinetics
  • Sponsors Novartis

    • Most Recent Events

    • 30 Mar 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