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Merck's new PAH drug, Winrevair, shows promise but raises concerns over high cost and bleeding risks.
Merck's drug, Winrevair, has shown significant benefits for patients with pulmonary arterial hypertension (PAH), a condition causing high blood pressure in the lungs.
In a late-stage study, it was found to reduce the risk of disease worsening, lung transplantation, or death.
Approved in the US and other countries, Winrevair is the first treatment targeting a specific protein called activin.
Despite its effectiveness, the drug, priced at about $238,000 annually, has raised concerns over potential bleeding risks.
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El nuevo medicamento para HAP de Merck, Winrevair, es prometedor, pero suscita preocupación por los altos costos y los riesgos de sangrado.