CompletedPhase 3NCT01223352

Effects of Two Dosing Regimens of Bosentan in Children With Pulmonary Arterial Hypertension

Studying Drug- or toxin-induced pulmonary arterial hypertension

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Key facts

Sponsor
Actelion
Principal Investigator
Andjela Kusic-Pajic, MD
Actelion
Intervention
bosentan(drug)
Enrollment
64 enrolled
Eligibility
12 years · All sexes
Timeline
20112013

Primary source

Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.

Open NCT01223352 on ClinicalTrials.gov

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