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Proven in a Broad Range of Patients1

GRIPHON is the largest adult PAH pivotal trial, studied as monotherapy, dual therapy (ERA or PDE5i), and triple therapy (ERA + PDE5i)1,2

Multicenter, long-term, double-blind, placebo-controlled, parallel-group, event-driven, phase 3 trial1,3

1156 Patients

UPTRAVI
(selexipag): n=574

Placebo:
n=582

Mean age:
48 years

Female:
80%

1.4 Years
(median duration of exposure to UPTRAVI)

Longest endpoint evaluation period of any prostacyclin pathway therapy

0.9 Years 

Median time from PAH diagnosis in patients taking UPTRAVI

New England Journal of Medicine Clinical Trial Publication for GRIPHON

This article includes information that has not been approved by the Food and Drug Administration for UPTRAVI. Please see full Prescribing Information available on this website. Authors[s] of this article have received remuneration from Actelion Pharmaceuticals US, Inc., or its affiliates.

UPTRAVI delays disease progression1

VIEW THE DATA

*Other=drugs and toxins (2%) and HIV (1%).

ERA=endothelin receptor antagonist; GRIPHON=Prostacyclin (PGI2) Receptor Agonist In Pulmonary Arterial HypertensION; HIV=human immunodeficiency virus; HPAH=heritable PAH; IPAH=idiopathic PAH; PAH=pulmonary arterial hypertension; PAH-CHD=PAH associated with congenital heart disease with repaired shunts; PAH-CTD=PAH associated with CTD; PDE5i=phosphodiesterase type-5 inhibitor.

References: 1. UPTRAVI (selexipag) full Prescribing Information. Actelion Pharmaceuticals US, Inc. 2. Data on file. Actelion Pharmaceuticals US, Inc. Length and Population Size of PAH Pivotal Trials. Confirmation. June 2024. 3. Sitbon O, Channick R, Chin KM, et al. Selexipag for the treatment of pulmonary arterial hypertension. N Engl J Med. 2015;373:2522-2533. 4. Sitbon O, Gomberg‍-‍Maitland M, Granton J, et al. Clinical trial design and new therapies for pulmonary arterial hypertension. Eur Respir J. 2019‍;‍53‍(‍1‍)‍:‍1801908. doi‍:‍10‍.‍1183‍/‍13993003‍.‍01908‍-‍2018 5. Data on file. Actelion Pharmaceuticals US, Inc. GRIPHON Baseline Characteristics Study Report.