Multicenter, Open-label, Non-comparative, Proof-of-concept, Phase 2a Study to Evaluate the Effect of a Single Infusion of Tezosentan on Pulmonary Vascular Resistance in Patients With Stable, Chronic Pulmonary Arterial Hypertension, Currently Not Treated With Endothelin Receptor Antagonists, Phosphodiesterase-5 Inhibitors or Prostacyclines
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
3
single infusion of tezosentan 5mg/h over 30 min corresponding to 2.5 mg
Washington University School of Medicine
St Louis, Missouri, United States
Baylor College of Medicine
Houston, Texas, United States
Hopital Antoine Béclère
Paris, Clamart, France
University Hospital of Basel, Clinic of Pneumology
Basel, Switzerland
Change in PVR from Baseline to 30 minutes expresses as percent of the Baseline value.
Time frame: 30 minutes
Change in mean right arterial pressure (mRAP) from Baseline to 30 minutes
Time frame: 30 minutes
Change in mPAP from Baseline to 30 min
Time frame: 30 minutes
Change in total pulmonary resistance (TPR) from Baseline to 30 min
Time frame: 30 minutes
Change in PCWP from Baseline to 30 min
Time frame: 30 minutes
Change in cardiac output (CO) from Baseline to 30 min
Time frame: 30 minutes
Change in cardiac index (CI) from Baseline to 30 min
Time frame: 30 minutes
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.
Centre Hospitalier Universitaire Vaudois (CHUV)
Lausanne, Switzerland