Medscape March 20, 2024
Megan Brooks

The US Food and Drug Administration (FDA) has approved aprocitentan (Tryvio) to lower blood pressure, in combination with other antihypertensive agents, in adults with treatment-resistant hypertension.

Aprocitentan is the first endothelin receptor antagonist approved for patients with hypertension. The recommended dose is 12.5 mg orally once daily, with or without food.

The efficacy and safety of aprocitentan were demonstrated in the phase 3 PRECISION study of 730 adults with systolic blood pressure ≥ 140 mmHg who were prescribed at least three antihypertensive medications.

Aprocitentan (12.5 mg daily) was well tolerated and statistically superior to placebo in lowering blood pressure at 4 weeks, with a sustained effect at 40 weeks.

Subgroup analyses showed that the blood pressure–lowering effect of aprocitentan...

Today's Sponsors

LEK
ZeOmega

Today's Sponsor

LEK

 
Topics: Biotechnology, FDA, Govt Agencies, Pharma, Pharma / Biotech
FDA warns GLP-1 compounder over safety rules
GLP-1 drug approvals: A breakdown
Rethinking FDA’s Accelerated Approval Pathway: New Draft Guidances and Implications for Drug Companies
FDA approves Novo Nordisk's Ozempic to treat chronic kidney disease in those with diabetes, expanding its use
Certainty vs. speed: How do patients feel about the tradeoff for new cancer drugs?

Share This Article