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?

Candesartan antihypertensive survival evaluation in Japan (CASE-J) trial of cardiovascular events in high-risk hypertensive patients

X
Trial Profile

Candesartan antihypertensive survival evaluation in Japan (CASE-J) trial of cardiovascular events in high-risk hypertensive patients

Status: Completed
Phase of Trial: Phase III

Latest Information Update: 17 Jan 2017

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 Candesartan cilexetil (Primary) ; Amlodipine
  • Indications Cardiovascular disorders; Hypertension
  • Focus Therapeutic Use
  • Acronyms CASE-J; CASE-J Ex
  • Most Recent Events

    • 06 Sep 2013 Additional lead trial centres added as reported by University Hospital Medical Information Network - Japan record.
    • 01 Dec 2011 Extension study results published in Hypertension Research.
    • 29 Aug 2010 Effects of pre-existing type 2 diabetes and CHD on outcomes presented at the Annual Congress of the European Society of Cardiology (ESC) 2010 meeting.

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