Selexipag was approved by the United States FDA on December 22, 2015 for the treatment of pulmonary arterial hypertension (PAH) to delay disease progression and reduce risk of hospitalization. PAH is a relatively rare disease with usually a poor prognosis requiring more treatment options to prolong long-term outcomes. Marketed by Actelion Pharmaceuticals und...
Selexipag is indicated for the treatment of pulmonary arterial hypertension (PAH) to delay disease progression and reduce risk of hospitalization.
Sheffield Teaching Hospitals NHS FT, Sheffield, United Kingdom
Jiangsu Province Hospital, Nanjing, China
The Republican Scientific-Practical Center ''Cardiology'', Minsk, Belarus
Minsk Regional Clinical Hospital Of The Red Banner Of Labor, Minsk, Belarus
Universidade de São Paulo, São Paulo, SP, Brazil
The Catholic University of Korea Seoul St Marys Hospital, Seoul, Korea, Republic of
The Republican Scientific-Practical Center ''Cardiology'', Minsk, Belarus
Minsk Regional Clinical Hospital, Minsk, Belarus
Uls Sao Joao - Hosp. Sao Joao, Porto, Portugal
Phoenix Children's Hospital, Phoenix, Arizona, United States
Uls Sao Jose - Hosp. Santa Marta, Lisboa, Portugal
Cleveland Clinic, Cleveland, Ohio, United States
Duke University Medical Center, Durham, North Carolina, United States
St. Vincent Medical Group, Inc., Indianapolis, Indiana, United States
Northwestern University Feinberg School of Medicine, Chicago, Illinois, United States
University of Pittsburgh Medical Center, Pittsburgh, Pennsylvania, United States
Institut Universitaire De Cardiologie Et De Pneumologie De Québec, Quebec, Canada
Clinical Pharmacology Unit (CPU), Merksem, Belgium
LA Biomedical Research Institute, Torrance, California, United States
Tufts Medical Center, Pulmonary/Critical Care & Sleep, Boston, Massachusetts, United States
University of Cincinnati, Heart, Lung and Vascular Institute, Cincinnati, Ohio, United States
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