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, double-blind, placebo controlled dose-ranging study of the effects of MK7418, both as monotherapy and in combination with furosemide, on diuresis and renal function in patients with congestive heart failure and renal impairment treated with oral loop diuretics who require hospitalization for fluid overload

Trial Profile

A randomized, double-blind, placebo controlled dose-ranging study of the effects of MK7418, both as monotherapy and in combination with furosemide, on diuresis and renal function in patients with congestive heart failure and renal impairment treated with oral loop diuretics who require hospitalization for fluid overload

Status: Completed
Phase of Trial: Phase II

Latest Information Update: 13 Dec 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 Rolofylline (Primary)
  • Indications Heart failure; Renal impairment
  • Focus Therapeutic Use
  • Sponsors NovaCardia
  • Most Recent Events

    • 28 Apr 2008 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