In the News

pulmonary advisor

Molecular Laboratory Test Can Discriminate Sepsis From Noninfectious SIRS

Design and results of clinical trials that led to FDA clearance of SeptiCyte™ LAB published in the American Journal of Respiratory and Clinical Care Medicine.

Product Briefs – SeptiCyte LAB

Immunexpress, Inc. published in the American Journal of Respiratory and Clinical Care Medicine the design and results of clinical trials validating SeptiCyte™ LAB in the discrimination of sepsis from non-infectious systemic inflammatory response syndrome (SIRS) in the Intensive Care Unit (ICU) of hospitals.
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Biocartis Partnership May Enable Immunexpress to Move Sepsis Test to Point of Care

Biocartis Group NV (‘Biocartis’), an innovative molecular diagnostics company and Immunexpress have entered into a partnership agreement aimed at the development and commercialization of Immunexpress’ SeptiCypte™ test for use on Biocartis’ sample-to-result Idylla™ platform.

Brief-Biocartis & Immunexpress Partnership For A Sepsis Host Immune Response Test

Immunexpress and Biocartis enter an agreement to develop and commercialize SeptiCyte™ technology for use on sample-to-result Idylla™  platform.
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Biocartis, Immunexpress Partner to Develop Sepsis Test

Biocartis and Immunexpress partner to develop a fully automated sepsis test, allowing for fast near-patient testing, resulting in potentially life-saving clinical information.

Biocartis, Immunexpress Partner to Develop Sepsis Test

Biocartis & Immunexpress sign partnership for a sepsis host immune response test on the Idylla™ platform.
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Differentiating sepsis and systemic inflammatory response syndrome using biomarkers

An interview with Dr. Richard Brandon, Chief Scientific Officer, Immunexpress, conducted by April Cashin-Garbutt, MA (Cantab).

Immunexpress wins FDA clearance for sepsis tests that could save billions of dollars

Immunexpress has won Food and Drug Administration clearance for a diagnostics test that could save hospitals billions of dollars. The FDA cleared SeptiCyte LAB analysis that tests for sepsis, a life-threatening immune response to infection.

FDA Clears SeptiCyte™ LAB for Suspected Sepsis Patients

The FDA granted 510(k) clearance to Immunexpress for the use of its SeptiCyte™ LAB as an aid in differentiating infection-positive (sepsis) from infection-negative (systemic inflammatory response syndrome, or SIRS) systemic inflammation in critically ill patients on their first day of intensive care unit admission.
Fierce Biotech

FDA clears Immunexpress’ RNA-based, whole-blood sepsis Dx

Immunexpress earned 510(k) clearance for its RNA-based clinical diagnostic that detects sepsis in critically ill patients. The test, which uses whole blood, returns results in a few hours.
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Immunexpress Receives FDA Clearance for Direct-From-Blood Sepsis Test

Revolutionary diagnostic SeptiCyte™ LAB cleared by FDA for suspected sepsis patients.

Speedy Sepsis Dx via Molecular Markers

To detect sepsis quickly, says Immunexpress, track the host response, not the pathogens. By Gail Dutton.