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.
Investigator Site, Gieres, France
Investigator Site, Kiel, Germany
University of Texas Southwestern Medical Center, Dallas, Texas, United States
Boston University Medical Center, Boston, Massachusetts, United States
Tufts Medical Center, Boston, Massachusetts, United States
University of Michigan Health System, Ann Arbor, Michigan, United States
Washington University School of Medicine, Saint Louis, Missouri, United States
Duke Unversity, Durham, North Carolina, United States
Investigator Site, Salford, United Kingdom
Covance Clinical Research Unit, Evansville, Indiana, United States
QPS, Groningen, Netherlands
The Ohio State University Medical Center, Columbus, Ohio, United States
"Instytut Gruźlicy i Chorób Płuc Klinika Chorób Wewnętrznych Klatki Piersiowej", Warszawa, Poland
"Instytut Kardiologii Collegium Medium UJ Krakowski Szpital Specjalistyczny im Jana Pawła II Klinika Chorób Serca i Naczyń", Krakow, Poland
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