ClinicalTrials.gov record
Enrolling by invitation Phase 3 Interventional

Long-Term Open-Label Extension Study of Oral Levosimendan

ClinicalTrials.gov ID: NCT07436689

Public ClinicalTrials.gov record NCT07436689. 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 May 20, 2026, 2:10 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 Multicenter, Open-Label, Long-Term Extension Study for Oral Levosimendan (TNX-103)

Study identification

NCT ID
NCT07436689
Recruitment status
Enrolling by invitation
Study type
Interventional
Phase
Phase 3
Lead sponsor
Tenax Therapeutics, Inc.
Industry
Enrollment
800 participants

Conditions and interventions

Interventions

  • TNX-103 Drug

Drug

Eligibility (public fields only)

Age range
Not listed
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
Mar 12, 2026
Primary completion
Feb 28, 2029
Completion
Feb 28, 2029
Last update posted
Mar 18, 2026

2026 – 2029

United States locations

U.S. sites
5
U.S. states
4
U.S. cities
5
Facility City State ZIP Site status
Tenax Investigational Site Chicago Illinois 60611
Tenax Investigational Site Minneapolis Minnesota 55455
Tenax Investigational Site Rochester Minnesota 55905
Tenax Investigational Site St Louis Missouri 63136
Tenax Investigational Site Charleston South Carolina 29425

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

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT07436689, 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 Mar 18, 2026 · Synced May 20, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT07436689 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →