Pulmonary Arterial Hypertension Clinical Trial
Official title:
An Open-label Extension of BPS-MR-PAH-203 in Pulmonary Arterial Hypertension (PAH) Patients
This is an open-label study for patients who participated in the BPS-MR-PAH-203 study and have volunteered to continue treatment for PAH with Beraprost Sodium Modified Release (BPS-MR) tablets.
Eligible patients who participated in BPS-MR-PAH-203 and who elect to continue receiving
study drug in an open-label extension.Each patient will return to the clinic following
enrollment in the study at 3, 6, and 12 months, and annually thereafter for assessment.
Patients will be called by study personnel to assess adverse events and concomitant
medications at Month 9, and at 3 month intervals following the annual visit.
At the End of Study visit, patients discontinuing study drug will be down-titrated off of
BPS-MR at the discretion of the Investigator, at a maximum decrement of one tablet (60µg)
b.i.d. per day and a minimum decrement of one tablet (60µg) b.i.d. per week. Likewise,
patients who withdraw early from the study will be down-titrated off of BPS-MR in the same
manner. Upon completion of down-titration, patients will return to the clinic for a final
Closeout visit.
Currently enrolled patients may be invited to participate in an optional four times daily
(QID) dosing substudy of BPS-MR with total daily dose of BPS-MR achieved previously in the
main study. Patients will return to the clinic for baseline visit, week 12, and then will
follow the visit schedule provided to them in BPS-MR-PAH-204 main study.
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