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LEVosimendan to Improve Exercise Limitation in Patients With PH-HFpEF

← catalyst calendar

NCT05983250

Sponsored by Tenax Therapeutics, Inc. (industry) · TENX — their whole pipeline →. With Medpace, Inc., Northwestern University.

Phase
Phase 3
Status
Active, not recruiting
Study type
Interventional
Design
Randomized · Quadruple · Treatment
Enrollment
230estimated
Sites
42
Countries
Canada, United States

Every value on this page is a field the sponsor filed with ClinicalTrials.gov, reproduced. Dates are their own estimates, revised as a study runs, unless the registry marks them actual. sources →

Source: ClinicalTrials.gov, retrieved 2026-08-19

Dates

each axis at the precision it was filed, with the registry's own basis
DateFiledBasisWhat it is
Start2024-01-10actualWhen the study began enrolling
Primary completion2026-06-30actualThe date the last participant is measured for the primary outcome — the readout window
Study completion2028-10-30estimatedThe whole study's end, after follow-up
First posted2023-08-09actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2026-07-24actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Condition

  • Pulmonary Hypertension

Interventions

  • Drug: TNX-103
  • Drug: Placebo

Primary outcome

what the primary-completion date above is the date OF
Change in Six-minute walk distance
measured 12 weeks

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