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. 2024 Mar 22;24(1):13–28. doi: 10.1007/s40268-024-00453-x
Pulmonary artery hypertension is a chronic disease associated with poor prognosis and a 5-year survival rate of about 50–60%.
Current treatments improve the prognosis, but they do not arrest the progression of disease and they are associated with significant adverse effects.
There is an immediate need for new clinical trials involving new drugs with enhanced efficacy and milder adverse effects.