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.
A Michigan Medicine-led study reveals that the once-feared severe complications that occur during balloon pulmonary angioplasty have dropped in recent years.
Adults treated with medication for chronic hypertension present before or during the first 20 weeks of pregnancy had fewer adverse pregnancy outcomes compared to adults who did not receive antihypertensive treatment.
A 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 MoreNew research from the American Heart Association revealed beta-blockers were not more likely to cause depression compared to other similar treatments, but the drugs may be linked to unusual dreams, insomnia and sleep disorders.
Read MoreJanssen Pharmaceutical Companies has submitted Uptravi (selexipag) as an injection for intravenous use for the treatment of pulmonary arterial hypertension.
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 MoreIn certain patients, measurements of pulmonary artery (PA) distensibility are more effective at detecting pulmonary hypertension due to left heart disease than measurements of PA dilatation.
Read MoreAmong 111,356 veterans with pulmonary hypertension, only 1,737 (1.6%) patients received pulmonary rehabilitation.
Read MoreThe patient was treated under an emergency IND filed by a qualified Investigator and approved by the US FDA, according to the manufacturer Vero Biotech.
Read MoreThe implantable Aria CV Pulmonary Hypertension System has received a breakthrough device designation from the FDA, according to the manufacturer Aria CV.
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