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Idorsia’s Tryvio Receives the US FDA’s Approval for the Treatment of Hypertension

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Idorsia’s Tryvio Receives the US FDA’s Approval for the Treatment of Hypertension

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  • The US FDA has approved Tryvio (12.5mg, oral, QD, with/without food) in addition with antihypertensive drugs to treat hypertensive adults not controlled on other drugs 
  • The P-III (PRECISION) trial assessed the efficacy of Tryvio for hypertensive adults with SBP ≥140 mmHg receiving at least 3 antihypertensive therapies with the 1EP as change in SiSBP at wk.4 & 2EP as change in SiSBP from wk.36 to wk.40 
  • In the study post 4wks. PBO run-in duration, patients (n=730) in part 1 were administered Tryvio (12.5mg, 25mg, or PBO, QD) for 4wks., all patients were then administered Tryvio (25mg, QD) for 32wks. in part 2 & post 32wks. patients were re-randomized to receive Tryvio (25mg) or PBO for a 12wk. withdrawal period in part 3 

Ref: Idorsia | Image: Idorsia

Related News:- Viatris Collaborates with Idorsia to Develop and Commercialize Selatogrel and Cenerimod

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Dipanshu Dixit

A passionate content writer with expertise in delivering high-quality and engaging content, Dipanshu is a keen reader and a versatile writer. Dipanshu dedicatedly covers news ranging from biopharma, life sciences, biotech, and MedTech to diagnostics and animal health companies, FDA, EMA, and biosimilar approvals. He can be contacted at connect@pharmashots.com

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