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Clinical Trial Summary

PH-HFpEF patients will receive weekly open-label doses of levosimendan and be periodically evaluated for safety and effectiveness in extended use.


Clinical Trial Description

This study will enroll PH-HFpEF patients that have completed a controlled levosimendan study. These patients will receive weekly open-label doses of levosimendan and be periodically evaluated for safety and effectiveness in extended use. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03624010
Study type Interventional
Source Tenax Therapeutics, Inc.
Contact
Status Active, not recruiting
Phase Phase 2
Start date November 14, 2018
Completion date February 2024

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