FDA Grants Orphan Drug Status to Pulmonary Arterial Hypertension Treatment
ZMA001, in development for pulmonary arterial hypertension, has been designated as an Orphan Drug by the US Food and Drug Administration.
ZMA001, in development for pulmonary arterial hypertension, has been designated as an Orphan Drug by the US Food and Drug Administration.
The 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.
Earlier detection of pulmonary hypertension in the community and expedited referral of high-risk or complex patients are recommended in the new ESC/ERS Guidelines for the diagnosis and treatment of pulmonary hypertension.
Patients with pulmonary hypertension and chronic obstructive pulmonary disease can now be identified by looking at three clinical variables, new research shows.
Read MoreA recent study highlights the importance of treating pulmonary hypertension in patients with obstructive sleep apnea.
Read MoreThe COVID-19 pandemic is associated with higher blood pressure levels among middle-aged adults across the US, according to research published in the journal Circulation.
Read MoreClinical trial and real-world data provide evidence that inhaled nitric oxide is effective for reducing pulmonary hypertension in the perioperative setting.Â
Read MoreA CVS subsidiary launched a program to help patients with pulmonary arterial hypertension (PAH) better manage their own care.
Read MorePatients who have chronic kidney disease and pulmonary hypertension are at a greater risk for a variety of adverse outcomes, according to new research.
Read MoreCan patients with pulmonary arterial hypertension and iron deficiency benefit from iron supplements?
Read MoreA new study, presented at the American Association for Thoracic Surgery’s annual meeting, found that patients treated surgically for segmental chronic thromboembolic pulmonary hypertension had positive outcomes.
Read MoreA new literature review looks at the role of pulmonary hypertension in people with pulmonary fibrosis.
Read MoreResults of a clinical trial show that patients with pulmonary hypertension (PH) have a lower capacity for exercise during hypoxia.
Read MoreHigh dose inhaled nitric oxide resulted in improvements in physical activity and other outcomes in patients at risk for pulmonary hypertension-associated fibrotic interstitial lung disease.
Read MoreA new study sheds light on the range of pulmonary vascular resistance associated with mortality and heart failure in certain patients at risk for pulmonary hypertension.
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