This study is to demonstrate the safety, tolerability, pharmakokinetic and pharmacodynamic effect of BAY63-2521 in patients with pulmonary hypertension and stable treatment of sildenafil 20 mg.
Study Type
INTERVENTIONAL
Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
7
The investigational drug will be given twice per subject, as single dose administration of BAY 63-2521 (0.5 mg and 1.0 mg) during the hemodynamic investigation.
Unnamed facility
Heidelberg, Baden-Wurttemberg, Germany
Unnamed facility
Löwenstein, Baden-Wurttemberg, Germany
Unnamed facility
Giessen, Hesse, Germany
Unnamed facility
Greifswald, Mecklenburg-Vorpommern, Germany
Unnamed facility
Impact of a single dose of BAY63-2521 on pharmacodynamic parameters of the pulmonary system, on safety, tolerability and pharmacokinetics.
Time frame: At baseline, throughout study days 1 and 2
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Dresden, Saxony, Germany