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Mineralys Therapeutics reported positive late-stage results for lorundrostat, with FDA acceptance of its application and a decision expected by December 2026.
Mineralys Therapeutics reported strong fourth-quarter 2025 results, with the FDA accepting lorundrostat’s NDA and setting a PDUFA target action date of December 22, 2026.
Pivotal trials showed a 6.2 mmHg systolic blood pressure reduction and favorable safety, though the drug didn’t meet its primary endpoint in a sleep apnea trial.
Cash and investments rose to $656.6 million by year-end, supporting operations through 2028.
Net loss narrowed to $154.7 million, and the company plans commercial launch targeting third- and fourth-line hypertension use, with intellectual property protection extending to at least 2035.
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Mineralys Therapeutics informó resultados positivos en etapas tardías para lorundrostat, con la aceptación de su aplicación por parte de la FDA y una decisión esperada para diciembre de 2026.