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Clinical Trial Summary

This is a two-part study evaluating the effectiveness of CRD-740 in patients with either Heart Failure with Reduced Ejection Fraction (HFrEF) or Heart Failure with Preserved Ejection Fraction (HFpEF) after 12 weeks of treatment. The primary objective in Part A is to assess the effect of CRD-740 compared to placebo in plasma cGMP at Week 4. The primary objective in Part B is to determine whether CRD-740 reduces NT-proBNP compared to placebo at Week 12.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05409183
Study type Interventional
Source Cardurion Pharmaceuticals, Inc.
Contact
Status Terminated
Phase Phase 2
Start date May 26, 2022
Completion date July 25, 2023

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