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Active, not recruiting Phase 3 Interventional

LEVosimendan to Improve Exercise Limitation in Patients With PH-HFpEF

ClinicalTrials.gov ID: NCT05983250

Public ClinicalTrials.gov record NCT05983250. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 20, 2026, 9:17 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Phase 3, Double-Blind, Randomized, Placebo-Controlled Study of Levosimendan in Pulmonary Hypertension Patients With Heart Failure With Preserved Left Ventricular Ejection Fraction (PH-HFpEF)

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

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).

Study identification

NCT ID
NCT05983250
Recruitment status
Active, not recruiting
Study type
Interventional
Phase
Phase 3
Lead sponsor
Tenax Therapeutics, Inc.
Industry
Enrollment
230 participants

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
18 Years to 85 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jan 10, 2024 (Actual)
Primary completion
Jun 30, 2026 (Actual)
Completion
Oct 30, 2028 (Estimated)
Last update posted
Jul 24, 2026

2024 – 2028

United States locations

U.S. sites
40
U.S. states
21
U.S. cities
35
Facility City State ZIP Site status
Tenax Investigational Site Tucson Arizona 85721 —
Tenax Investigational Site La Jolla California 92037 —
Tenax Investigational Site Los Angeles California 90033 —
Tenax Investigational Site Los Angeles California 90048 —
Tenax Investigational Site Sacramento California 95817 —
Tenax Investigational Site San Francisco California 94143 —
Tenax Investigational Site Torrance California 90502 —
Tenax Investigational Site Jacksonville Florida 32224 —
Tenax Investigational Site Winter Haven Florida 33881 —
Tenax Investigational Site Atlanta Georgia 30322 —
Tenax Investigational Site Chicago Illinois 60208 —
Tenax Investigational Site Chicago Illinois 60637 —
Tenax Investigational Site Galesburg Illinois 61401 —
Tenax Investigational Site Indianapolis Indiana 46202 —
Tenax Investigational Site Indianapolis Indiana 46260 —
Tenax Investigational Site Louisville Kentucky 40202 —
Tenax Investigational Site Boston Massachusetts 02114 —
Tenax Investigational Site Minneapolis Minnesota 55455 —
Tenax Investigational Site Rochester Minnesota 55905 —
Tenax Investigational Site St Louis Missouri 63136 —
Tenax Investigational Site Omaha Nebraska 68198 —
Tenax Investigational Site New York New York 10021 —
Tenax Investigational Site New York New York 10029 —
Tenax Investigational Site Rochester New York 14621 —
Tenax Investigational Site Roslyn New York 11576 —
Tenax Investigational Site Durham North Carolina 27710 —
Tenax Investigational Site Greensboro North Carolina 27401 —
Tenax Investigational Site Cincinnati Ohio 45267 —
Tenax Investigational Site Columbus Ohio 43214 —
Tenax Investigational Site Pittsburgh Pennsylvania 15212 —
Tenax Investigational Site Providence Rhode Island 02903 —
Tenax Investigational Site Charleston South Carolina 29425 —
Tenax Investigational Site Columbia South Carolina 29044 —
Tenax Investigational Site Dallas Texas 75204 —
Tenax Investigational Site Dallas Texas 75390 —
Tenax Investigational Site Lubbock Texas 79430 —
Tenax Investigational Site Plano Texas 75093 —
Tenax Investigational Site Murray Utah 84107 —
Tenax Investigational Site Richmond Virginia 23298 —
Tenax Investigational Site Madison Wisconsin 53792 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 2 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT05983250, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jul 24, 2026 · Synced Oct 20, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT05983250 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →