Ralinepag Reduced Pulmonary Arterial Hypertension Progression
Phase 3 trial results show ralinepag significantly reduced the risk of worsening symptoms and improved exercise capacity in pulmonary arterial hypertension patients.
Phase 3 trial results show ralinepag significantly reduced the risk of worsening symptoms and improved exercise capacity in pulmonary arterial hypertension patients.
Phase 3 trial results show ralinepag significantly reduced the risk of worsening symptoms and improved exercise capacity in pulmonary arterial hypertension patients.
Read MoreData from clinical trials investigating treatments for pulmonary hypertension and pulmonary fibrosis will be highlighted at ATS 2026.
Read MoreThe Ulspira Solution combines inhaled nitric oxide (iNO) gas with a portable delivery system and clinical support to treat infants with hypoxic respiratory failure.
Read MoreInsmed will present four abstracts on treprostinil palmitil inhalation powder (TPIP), being evaluated as a once-daily therapy for the treatment of patients with PAH, PH-ILD, and other rare and serious pulmonary disorders.
Read MoreWinrevair is now FDA-approved to treat pulmonary arterial hypertension to improve exercise capacity and reduce the risk of clinical worsening events, including hospitalization for PAH, lung transplantation and death.
Read MoreGLP-1 RAs may provide added benefit over SGLT2-i in protecting right heart function among patients with PAH.
Read MoreTreatment with an inhaled dry powder formulation of treprostinil was associated with improvements in cardiac effort for patients with pulmonary hypertension–interstitial lung disease (PH-ILD).
Read MoreResults from a Phase 3 clinical study of adults with pulmonary arterial hypertension found Winrevair reduced the risk of clinical worsening events by 76%.
Read MoreIn this edition of our “Industry Analysis” series, RT magazine speaks with manufacturers of inhaled nitric oxide delivery systems about the latest market innovations in the iNO industry.
Read MorePulmonary artery denervation (PADN) could reduce mean right atrial pressure, mean pulmonary artery pressure, and pulmonary vascular resistance in pulmonary hypertension patients.
Read MoreZMA001, in development for pulmonary arterial hypertension, has been designated as an Orphan Drug by the US Food and Drug Administration.
Read MoreUse of hormone replacement therapy (HRT) in women was associated with lower mean pulmonary artery pressure and higher right ventricular fractional shortening and right ventricular ejection fraction, according to research presented at ATS 2024.
Read MoreThe injection on top of background therapy significantly improved exercise capacity and multiple secondary outcome measures compared to background therapy alone.
Read MoreAria CV Inc reports its first patient was implanted with the Gen 2 Aria CV Pulmonary Hypertension System.
Read MoreInfusions of potentially therapeutic cells derived from the heart are safe for people with pulmonary arterial hypertension, according to a study led by Cedars-Sinai investigators.
Read MoreThe Pulmonary Fibrosis Foundation and Pulmonary Hypertension Association have developed a position statement that addresses gaps in the diagnosis and treatment of patients living with pulmonary hypertension related to interstitial lung disease.
Read MoreThe Pulmonary Fibrosis Foundation announced Franck Rahaghi, MD, MHS, FCCP, as its incoming president, CEO, and chief medical officer, effective Sept 15.
Read MoreThe latest guideline from the American Thoracic Society reaffirms benefits for patients with COPD as well as pulmonary hypertension and interstitial lung disease.
Read MoreThe recall was issued due to a misalignment of the check valve in the device’s manifold, which may cause the manifold to fail and interrupt therapy to neonates.
Read MoreThe Janssen Pharmaceutical Companies of Johnson & Johnson is seeking FDA approval of an investigational single-tablet combination therapy of macitentan and tadalafil for the long-term treatment of pulmonary arterial hypertension.
Read MoreThe new guide can assist providers in learning and practicing skills to prevent or manage respiratory symptoms in patients with chronic lung disease.
Read MoreA Michigan Medicine-led study reveals that the once-feared severe complications that occur during balloon pulmonary angioplasty have dropped in recent years.
Read MoreRT magazine spoke with manufacturers of inhaled nitric oxide delivery systems about the latest market innovations in the iNO industry, specifically about the impact of cylinder-free (“tankless”) systems, plus research on its potential use to treat other cardiopulmonary diseases.
Read MoreThe outcomes for patients with pulmonary arterial hypertension taking macitentan and tadalafil together in a single pill have been detailed in a new study, which shows significant improvement compared to those taking either drug alone.
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