News

PAH Drug Sildenafil Seen to Work Well with Ambrisentan as Combo Therapy

A recent Japanese study suggested that it might be more advantageous to combine sildenafil with ambrisentan than with bosentan as a therapy for patients with pulmonary arterial hypertension (PAH). Researchers found that bosentan reduced the concentration of sildenafil in the plasma when the drugs were taken together, while sildenafil combined with ambrisentan…

Pulmonary Hypertension Association Asks Public to Support Pacing Parson’s 1,000-Mile Walk

Don Stevenson, also known as the Pacing Parson, is marking his 80th birthday with a 1,000-mile benefit and awareness walk for the Pulmonary Hypertension Association (PHA), a nonprofit group dedicated to extending and improving the lives of those affected by pulmonary hypertension (PH). The PHA is asking the public to support Stevenson in his efforts.

3 PH Centers Newly Accredited by PHCC for High Level of Patient Care

The Pulmonary Hypertension Association (PHA) announced that three more centers recently received Pulmonary Hypertension Care Center (PHCC) accreditation, raising the total number of PHA-accredited clinics to 32 across the U.S. In addition to acknowledging a high level of patient care, accreditation allows these centers to contribute to the Pulmonary Hypertension Association Registry…

PAH Oral Prostacyclin Analog Drugs, Like Treprostinil, Are Improving But Have Way to Go

Prostacyclin analogs have substantially improved pulmonary arterial hypertension (PAH) treatment, but the use of these drugs is hampered by the difficulties and risks of treating patients with continuous intravenous infusions. A new overview highlighted the development of oral prostacyclins, focusing on the drug treprostinil (Orenitram). The overview was published under the…

Newly Diagnosed PAH Patients at Risk of More Rapid Disease Progression

People newly diagnosed with pulmonary arterial hypertension (PAH) are at greater risk of disease progression than PAH patients sick for more than six months, a finding that highlights the importance of early treatment, researchers reported. Their study, “Incident and prevalent cohorts with pulmonary arterial hypertension: insight from SERAPHIN“, was published in the…

Oral Selexipag Approved in Canada for PAH

Actelion Pharmaceuticals, Ltd., recently announced that the selective IP receptor agonist Uptravi (selexipag) has been granted Notice of Compliance (NOC) approval by Health Canada for the treatment of pulmonary arterial hypertension (PAH). Uptravi (selexipag) was originally discovered and synthesized by Nippon Shinyaku as an oral, prostacyclin receptor agonist formulated…

Gene’s Absence Found to Induce PAH in Mouse Study

A study from the University of Alabama at Birmingham showed that the immune receptor TLR4 is important for regulating the development of pulmonary arterial hypertension (PAH). Mice lacking the gene for TLR4 spontaneously developed PAH, indicating a protective role for the immune factor. Chronic hypoxia — low levels of oxygen —…

Phaware Teams with Super Bowl 50 for 2016 PH Awareness Contest

The phaware global association knows the soon-to-be-played Super Bowl 50 will attract plenty of fans and attention — and it’s teaming with the biggest sporting event in the U.S. (and a popular one elsewhere) to kick off its 2016 pulmonary hypertension global awareness campaign — Engage for a Cure — with the BIG GAME…

PAH Drug May Not Be of Added Benefit to Infants After Heart Surgery

Pulmonary arterial hypertension (PAH) is a common condition in infants undergoing surgery for congenital heart defects, and it is a main contributor to morbidity and death following surgery. For this reason, the drug iloprost is often given these infants after surgery, as it is known to induce blood vessel relaxation and decrease…