Results 61 to 70 of about 1,848 (184)

Selexipag for pulmonary arterial hypertension in a wide range of adult congenital heart disease

open access: yesInternational Journal of Cardiology Congenital Heart Disease, 2021
Background: Selexipag has been recognised as effective treatment for pulmonary arterial hypertension (PAH). However, evidence for its use in PAH associated with congenital heart disease (CHD) is limited to those with PAH after simple defect correction ...
Alexandra C. van Dissel   +6 more
doaj   +1 more source

Evidence for PDZ‐Binding Kinase in Lung Disease With an Emphasis on PAH

open access: yesPulmonary Circulation, Volume 16, Issue 3, July 2026.
ABSTRACT Originally named T‐cell‐originated Lymphokine‐activated killer protein kinase (TOPK), PDZ‐Binding Kinase (PBK) is a serine/threonine kinase that is a member of the family of mitogen‐activated protein kinases (MAPKKs), which is overexpressed in lung cancer and interstitial pulmonary fibrosis (IPF). Along these lines, recent work also shows that
Scott A. Barman   +2 more
wiley   +1 more source

Population pharmacokinetics of selexipag for dose selection and confirmation in pediatric patients with pulmonary arterial hypertension

open access: yesCPT: Pharmacometrics & Systems Pharmacology
Selexipag is an oral selective prostacyclin receptor agonist approved for the treatment of pulmonary arterial hypertension (PAH) in adults. To date, no treatment targeting the prostacyclin pathway is approved for pediatric patients.
Lene Nygaard Axelsen   +3 more
doaj   +1 more source

Effectiveness of PAH Specific Treatment Is Comparable Between PAH Associated With Connective Tissue Disease and Idiopathic PAH: Data From the Multicentre National Registry

open access: yesPulmonary Circulation, Volume 16, Issue 3, July 2026.
ABSTRACT Pulmonary arterial hypertension (PAH) is a rare disease with poor prognosis. The same treatment is recommended in patients with PAH associated with connective tissue disease (CTD) and idiopathic PAH (IPAH). However, the effectiveness of PAH‐specific treatment in these both groups is inconsistent.
Anna Smukowska‐Gorynia   +26 more
wiley   +1 more source

Determining the value contribution of selexipag for the treatment of pulmonary arterial hypertension (PAH) in Spain using reflective multi-criteria decision analysis (MCDA)

open access: yesOrphanet Journal of Rare Diseases, 2018
Background Pulmonary Arterial Hypertension (PAH) is a chronic rare disease that can lead to serious cardiovascular problems and death. Additional treatments that increase effectiveness, that are safe and with a convenient administration that improve ...
Alberto Jiménez   +3 more
doaj   +1 more source

The Role of Medical Therapy Before and After Balloon Pulmonary Angioplasty: CTEPH AC Registry Across Japan

open access: yesPulmonary Circulation, Volume 16, Issue 3, July 2026.
ABSTRACT We aimed to evaluate the role of medical therapy before and after balloon pulmonary angioplasty (BPA) for non‐operable chronic thromboembolic pulmonary hypertension (CTEPH) in the modern management era. This Japanese nationwide, multicenter, prospective observational registry, including 37 centers, analyzed data newly registered from August ...
Miki Sakamoto‐Iwata   +23 more
wiley   +1 more source

Datasheet1_A Canadian, retrospective, multicenter experience with selexipag for a heterogeneous group of pediatric pulmonary hypertension patients.pdf

open access: yes, 2023
IntroductionSelexipag, an oral nonprostanoid prostaglandin receptor agonist, has led to reduced morbidity and mortality in adults with pulmonary arterial hypertension (PAH). While the adult literature has been extrapolated to suggest selexipag as an oral
Martin Hosking (4983554)   +8 more
core   +1 more source

Impact of selexipag maintenance dose on persistence, adherence, and hospitalization in US patients with pulmonary arterial hypertension

open access: yesPulmonary Circulation
Selexipag is an oral selective agonist of the prostacyclin receptor approved to treat adults with pulmonary arterial hypertension (PAH). Selexipag is initiated at a dose of 200 μg twice daily (bid) and usually titrated up by 200 μg bid weekly (per label)
Charles D. Burger   +3 more
doaj   +1 more source

Observed Weight Gain in Patients With Pulmonary Arterial Hypertension Treated With Sotatercept

open access: yesPulmonary Circulation, Volume 16, Issue 3, July 2026.
ABSTRACT Sotatercept, an activin signaling inhibitor for pulmonary arterial hypertension (PAH), has demonstrated significant improvements in clinical outcomes though its off‐target effects are still an area for discovery. Anecdotal increases in total body weight not attributable to fluid retention have been observed.
Rebecca A. Greene   +12 more
wiley   +1 more source

Efficacy and Safety of Selexipag in Adults With Raynaud's Phenomenon Secondary to Systemic Sclerosis:A Randomized, Placebo-Controlled, Phase II Study [PDF]

open access: yes, 2017
Objective: To determine the effect of selexipag, an oral, selective IP prostacyclin receptor agonist, on the frequency of attacks of Raynaud's phenomenon (RP) in patients with systemic sclerosis (SSc).
Schwarting, A   +25 more
core   +1 more source

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