The aim of this study is to understand the treatment patterns in patients with Pulmonary Arterial Hypertension (PAH) or Chronic Thromboembolic Pulmonary Hypertension (CTEPH) during a switch of treatment to Adempas in real-life clinical practice. In addition, this study will describe patient demographics and reason for switching
Study Type
OBSERVATIONAL
Enrollment
125
As per the treating physicians discretion
Unnamed facility
Many Locations, Belgium
Unnamed facility
Many Locations, Canada
Unnamed facility
Many Locations, Colombia
Unnamed facility
Many Locations, Germany
Unnamed facility
Starting Dose
Time frame: Up to a total of 8 weeks of titration period
Dose Increments
Time frame: Up to a total of 8 weeks of titration period
Final Dose
Time frame: Up to a total of 8 weeks of titration period
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Many Locations, Japan
Unnamed facility
Many Locations, Sweden
Unnamed facility
Many Locations, Turkey (Türkiye)