A Study of Selexipag in Participants Who Participated in a Previous Selexipag Study

PHASE3CompletedINTERVENTIONAL
Enrollment

43

Participants

Timeline

Start Date

May 3, 2021

Primary Completion Date

November 10, 2023

Study Completion Date

November 10, 2023

Conditions
Hypertension, Pulmonary
Interventions
DRUG

Selexipag

Selexipag tablets will be administered orally at all dose strengths (200, 400, 600, 800, 1000, 1200, 1400 and 1600 microgram) twice daily.

Trial Locations (13)

813

Kaohsiung Veterans General Hospital, Kaohsiung City

10002

National Taiwan University Hospital, Taipei

21565

Gachon University Gil Medical Center, Incheon

220036

The Republican Scientific-Practical Center ''Cardiology'', Minsk

220143

Minsk Regional Clinical Hospital, Minsk

380015

Sanjivani Hospitals, Ahmedabad

600006

Apollo Hospitals, Chennai

050152

Institutul de pneumoftiziologie Marius Nasta, Bucharest

06351

Samsung Medical Center, Seoul

06591

The Catholic University of Korea Seoul St Marys Hospital, Seoul

Unknown

Municipal Inst. Of Dnipropetrovsk Region. Council, Dnipro

Health Care Municipal Institution City Clinical Hospital #13, Kharkiv

03680

State Institute Of Phthisiology And Pulmonology N.A. F.G. Yanovskiy Of Ams Ukraine, Kyiv

Sponsors

Lead Sponsor

All Listed Sponsors
lead

Actelion

INDUSTRY

NCT04565990 - A Study of Selexipag in Participants Who Participated in a Previous Selexipag Study | Biotech Hunter | Biotech Hunter