Study to Evaluate the Efficacy and Safety of AZD4831 in Participants With Heart Failure With Left Ventricular Ejection Fraction > 40% (ENDEAVOR)

  • STATUS
    Recruiting
  • End date
    Nov 13, 2024
  • participants needed
    1485
  • sponsor
    AstraZeneca
Updated on 7 October 2022

Summary

This is a randomised, double-blind, placebo-controlled, multi-center sequential phase 2b and Phase 3 study to evaluate the efficacy and safety of AZD4831 administered for up to 48 Weeks in participants with heart failure with left ventricular ejection fraction > 40%. The study will consist of 2 separate parts, Part A and Part B, approximately 660 participants will be randomised in Part A, 825 in Part B.

Details
Condition Heart Failure With Preserved Ejection Fraction
Treatment Placebo, AZD4831
Clinical Study IdentifierNCT04986202
SponsorAstraZeneca
Last Modified on7 October 2022

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If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

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Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

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