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?

Deliver Insights in Hypertrophic Cardiomyopathy and Observational Outcomes in Real World: United States Prospective Registry Study

Next Previous
X
Search
Trial Profile

Deliver Insights in Hypertrophic Cardiomyopathy and Observational Outcomes in Real World: United States Prospective Registry Study

Status: Recruiting
Phase of Trial: Phase IV

Latest Information Update: 20 Dec 2024

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 Mavacamten (Primary) ; Beta adrenergic receptor antagonists; Disopyramide
  • Indications Hypertrophic cardiomyopathy
  • Focus Therapeutic Use
  • Acronyms DISCOVER-HCM
  • Sponsors Bristol-Myers Squibb

    • Most Recent Events

    • 17 Dec 2024 Planned End Date changed from 15 Aug 2029 to 17 Aug 2029.
    • 17 Dec 2024 Planned primary completion date changed from 15 Aug 2029 to 17 Aug 2029.
    • 12 Oct 2022 Planned End Date changed from 31 Jul 2029 to 15 Aug 2029.

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