News

Researchers Discover Ranolazine May Be a Viable PAH Therapy

A new study published in August’s issue of Cardiovascular Research, entitled “Ranolazine prevents INaL enhancement and blunts myocardial remodeling in a model of pulmonary hypertension” suggests ranolazine (RAN) as a potential therapeutic agent in the treatment of PAH pathology. Pulmonary arterial hypertension (PAH) is a result of…

Can Pulmonary Hypertension Be Treated With a Plant?

Pulmonary hypertension is a life-threatening, progressive disease that, to this day, is still incurable. Recently, a team of researchers turned to nature for answers, experimenting with extracting a protective enzyme from plant leaves that may hold the key to making a novel treatment work. Lead author and assistant…

Discovery Channel To Air Documentary on Idiopathic Pulmonary Fibrosis

Every Breath Counts: Idiopathic Pulmonary Fibrosis, a documentary to mark Pulmonary Fibrosis Awareness Month, will air on the Discovery Channel on September 13th and 27th at 8:00 am ET/PT. Supported by Boehringer Ingelheim Pharmaceuticals, Inc. and created together with the Pulmonary Fibrosis Foundation and the Coalition for Pulmonary Fibrosis, the…

Treating Inflammation in PAH Using Antioxidant Inflammation Modulators

Pulmonary Arterial Hypertension (PAH) is a life-threatening disease in which endothelial dysfunction, vasoconstriction in small pulmonary arteries, dysregulated proliferation of vascular cells, and dysregulated inflammatory signaling leads to pulmonary arterial obstruction increasing pulmonary vascular resistance and resulting in right ventricular failure. Different types of treatments for PAH exist that can…

Bayer’s Adempas For CTEPH, PAH Confirmed Safe & Effective in Long-Term Studies

Findings collected during more than two years confirming the safety and efficacy of Bayer’s Adempas® (riociguat) in treating either inoperable or persistent/recurrent chronic thromboembolic pulmonary hypertension (CTEPH), and patients with pulmonary arterial hypertension (PAH) were recently presented at the European Respiratory Society (ERS) Congress. Riociguat is the first member of…

Phase I Trial of Pluristem’s PLX-PAD Cells for Pulmonary Arterial Hypertension Advances To Second Cohort Dosing

Photo Caption: “The Process is the product” – Pluristem’s 3D expansion technology allows for the production of different PLX cell products. Photo credit: Pluristem Therapeutics Inc. Haifa, Israel based Pluristem Therapeutics Inc. a drug developer specializing in placenta-based cell therapy products, has announced that licensee partner United Therapeutics…

New Study Outlines Potential PH Therapy Targets

Pulmonary hypertension is a condition caused by increased pressure in the pulmonary arteries. In advanced cases, its symptoms (shortness of breath, tiredness, chest pain) worsen and may limit all physical activity. Now, researchers from University of California, Los Angeles have developed a successful treatment to rescue advanced forms of…