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?

An open-label, single-sequence crossover study of DS-8500a to evaluate the effects on the pharmacokinetics of atorvastatin in Japanese healthy subjects

Next Previous
X
Search
Trial Profile

An open-label, single-sequence crossover study of DS-8500a to evaluate the effects on the pharmacokinetics of atorvastatin in Japanese healthy subjects

Status: Completed
Phase of Trial: Phase I

Latest Information Update: 23 Jul 2019

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 Firuglipel (Primary) ; Atorvastatin
  • Indications Type 2 diabetes mellitus
  • Focus Pharmacokinetics
  • Sponsors Daiichi Sankyo Company

    • Most Recent Events

    • 18 Jul 2019 Results assessing the effects of repeated oral administration of DS-8500a 75 mg on the pharmacokinetics of rosuvastatin and atorvastatin in healthy adults, published in the Clinical Drug Investigation
    • 16 Jun 2016 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