The purpose of this study is to provide continued access to treatment with oral levosimendan (TNX-103) and to describe the safety of continued use of TNX-103 in participants with pulmonary hypertension with heart failure with preserved left ventricular ejection fraction (PH-HFpEF) who received TNX-103 in a parent study.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
800
Open-label oral levosimendan 1-3mg
Tenax Investigational Site
Chicago, Illinois, United States
Tenax Investigational Site
Minneapolis, Minnesota, United States
Tenax Investigational Site
Rochester, Minnesota, United States
Tenax Investigational Site
St Louis, Missouri, United States
The incidence (i.e., the percentage of patients who experience at least 1 occurrence) of select AE/SAEs
The incidence (i.e., the percentage of patients who experience at least 1 occurrence) of select AE/SAEs will be tabulated by system organ class and preferred term.
Time frame: From enrollment through study completion (up to 3 years)
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Tenax Investigational Site
Charleston, South Carolina, United States