vimarsana.com

Cytovale Inc News Today : Breaking News, Live Updates & Top Stories | Vimarsana

Cytovale s Intellisep rules out sepsis in 97 5% of cases

Cytovale Inc. has posted a feverish run of wins lately. The company gained U.S. FDA clearance for its Intellisep rapid test for sepsis in January 2023, raised $84 million in a series C in November and just published results showing the test has negative predictive value of 97.5%.

Inflammatix sepsis test scores FDA breakthrough device designation

Inflammatix Inc. received U.S. FDA breakthrough device designation for its Triverity acute infection and sepsis test system, which produces three readouts that could help emergency physicians quickly determine the proper course of treatment.

Cytovale raises $84M to commercialize sepsis diagnostic

The time to diagnosis of sepsis infection to a patient in the hospital can be critical, with underdiagnosis resulting in rapid deterioration, risk of organ damage and need for readmission, and overdiagnosis leading to the avoidable and sometimes serious health consequences of overtreating patients with broad-spectrum antibiotics.

© 2025 Vimarsana

vimarsana © 2020. All Rights Reserved.