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This study will evaluate the efficacy of TNX-103 (oral levosimendan) compared with placebo in subjects with PH-HFpEF as measured by the change in 6-Minute Walk Distance (6 MWD; Day 1 to Week 12).
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Lead Sponsor
Tenax Therapeutics, Inc.
Collaborators
NCT05746039 · Obesity, Interstitial Lung Disease, and more
NCT03854071 · Heart Failure, Pulmonary Hypertension, and more
NCT07073820 · Pulmonary Hypertension
NCT07477197 · Adult Congenital Heart Disease, Pulmonary Hypertension, and more
NCT06899815 · Pulmonary Hypertension
Tenax Investigational Site
Tucson, Arizona
Tenax Investigational Site
La Jolla, California
Tenax Investigational Site
Los Angeles, California
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Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.
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