News

Pulmonary Hypertension Trailblazer Dr. Stuart Rich is New Program Director at Northwestern Medicine

Northwestern Medicine has appointed Dr. Stuart Rich as director of the newly launched Pulmonary Vascular Disease Program at the Bluhm Cardiovascular Institute, where he will also serve as professor of medicine-cardiology at Northwestern University Feinberg School of Medicine. Dr. Rich, an accomplished innovator in the field of pulmonary hypertension, brings over…

Promising Genetically-Enhanced Stem Cell Therapy for Pulmonary Arterial Hypertension Discovered

A new study recently published in the journal Circulation Research revealed encouraging results in the world’s first clinical trial using a genetically-enhanced stem cell therapy for pulmonary arterial hypertension (PAH). The study is entitled “Endothelial NO-Synthase Gene-Enhanced Progenitor Cell Therapy for Pulmonary Arterial Hypertension: the…

MUSC and Bristol-Myers Squibb Partner for Fibrotic Disease Research

Bristol-Myers Squibb Company and the Medical University of South Carolina recently signed a translational research partnership that will focus on fibrotic diseases, such as scleroderma, renal fibrosis, and idiopathic pulmonary fibrosis. This collaboration will also cover studies developed to further explore the disease mechanism of fibrosis, patient segmentation, and their…

OFEV (nintedanib) Added To Updated International Treatment Guidelines for Idiopathic Pulmonary Fibrosis (IPF)

Revised international treatment guidelines for Idiopathic Pulmonary Fibrosis (IPF) suggest use of OFEV (nintedanib), a proprietary drug from Ingelheim, Germany, based Boehringer Ingelheim Corporation for the treatment of the disease. This newly-added recommendation places high value on potential benefits of OFEV on patient-important outcomes such as slowing of disease…

Arginine Therapy May Alleviate PH in Thalassemia Patients

The amino acid arginine may contribute to pulmonary hypertension in patients with thalassemia, a disorder that leads to abnormal oxygenation of blood. A team of researchers from the Thalassemia Clinical Research Network conducted a study demonstrating that abnormal release of the enzyme arginase leads to a lack of bioavailable arginine,…

SteadyMed’s Trevyent for PAH Completes Human Factors Studies Validating Usability and Safety

Specialized Pharmaceutical Company SteadyMed Ltd. recently announced the completion of its program on human factors studies involving its flagship product candidate, Trevyent (treprostinil sodium), which is currently undergoing testing as a potential new treatment for pulmonary arterial hypertension (PAH). Trevyent is currently the only FDA-approved parenteral treatment for PAH, deliverable…


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