News

SteadyMed’s Treyvent Awarded Orphan Drug Designation from FDA

SteadyMed, Ltd., a company that develops products to treat orphan and high-value conditions with unmet parenteral delivery needs, recently announced that its lead product candidate, Trevyent® has been granted Orphan Drug Designation by the U.S. Food and Drug Administration (FDA) for the treatment of pulmonary arterial hypertension (PAH).

New PAH Drug from Actelion Approved by FDA

According to a recent announcement, the United States Food and Drug Administration (FDA) approved Actelion Pharmaceuticals’ Uptravi (selexipag) tablets for the treatment of adult patients with pulmonary arterial hypertension (PAH) to delay disease progression and reduce the risk of hospitalization, under orphan drug designation. PAH is a life-threatening disease…

Tackling New Zealand Alps to Promote PH Awareness, Research

Team PHenomenal Hope will take part in a seven-day cycling competition to raise awareness of pulmonary hypertension (PH) and money to advance research into the disease. The nonprofit, presented by the University of Pittsburgh Medical Center (UPMC), Bayer Healthcare, and Actelion, is competing in the The Pioneer race through New Zealand’s Southern Alps.

Sildenafil’s Use in Children with Pulmonary Arterial Hypertension Still Topic of Controversy

Sildenafil (Revatio) — a phosphodiesterase type-5 inhibitor developed by Pfizer – is approved for the treatment of pulmonary arterial hypertension (PAH) in adults. Two large international clinical trials, the STARTS I and II trials, subsequently investigated the safety of sildenafil use in children. Based on their findings, however, the U.S. Food and Drug Administration (FDA) and the…

Top 10 Most Read Pulmonary Hypertension Articles of 2015

Pulmonary Hypertension News has covered news surrounding the latest treatments, events, clinical trials, and research updates related to pulmonary hypertension on a daily basis throughout the past year. As the year of 2015 comes to an end, our “Top 10 Most Read Pulmonary Hypertension Articles of 2015” ranks the…

Two Common PAH Treatment Approaches May Be Equally Valid

Researchers in Turkey evaluated the two drug therapy approaches commonly used to treat pulmonary arterial hypertension (PAH) and found no substantial difference between the two in the patients observed. The study, titled “Combination Therapy in Pulmonary Arterial Hypertension: Single Centre Long-term Experience“ appeared in May 2015 in the West…

Systemic Sclerosis and Lung Fibrosis Study of Nintedanib Enrolls First Patient

Boehringer Ingelheim recently announced the enrollment of the first patient in its global, double-blind, randomized, and placebo-controlled SENSCIS (Safety and Efficacy of Nintedanib in Systemic SClerosIS) Phase 3 clinical trial. The trial (NCT02597933) is now enrolling patients, and is evaluating the safety and the efficacy of nintedanib in patients with systemic sclerosis (SSc)…

Pulmonary Hypertension Researchers Win 2015 Deutscher Zukunftspreis

German President Joachim Gauck has awarded the 2015 Deutscher Zukunftspreis, which honors innovation in science and technology, to a pulmonary hypertension (PH) research team that discovered and developed a drug effective in the treatment of two serious types of the disease. The winning team — led by Professor Ardeschir Ghofrani from the University Clinic…

Eiger BioPharmaceuticals’ PAH Therapy Bestatinâ„¢ (Ubenimex) Receives Notice of Allowance for U.S. Patent

Eiger BioPharmaceuticals, Inc. recently announced in a press release that a Notice of Allowance from the United States Patent and Trademark Office (USPTO) has been issued for the U.S. patent application 13/829,321, titled “Treatment of Pulmonary Hypertension with Leukotriene Inhibitors” covering Bestatinâ„¢ (ubenimex), a leukotriene A4hydrolase (LTA4H) inhibitor, for treating…