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Science, technology and the emergence of AI have converged to make precision medicine for acute care a reality. This is how we deliver healthcare tailored to biology.

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The Sepsis ImmunoScore® Predicts Sepsis, Mortality, and Deterioration Better than Clinical Scores and Widely Available Biomarkers

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Prenosis is developing a pipeline of integrated diagnostics and therapeutics grounded in each patient's unique biological profile, using deep data science and AI to give clinicians tools that reflect the true complexity of critical disease.

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Sepsis ImmunoScore®

BioAegis Therapeutics Announces Collaboration with Prenosis to Advance AI-Driven Precision Medicine in Inflammatory Disease

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Treating the Patient, Not the Disease

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Sepsis ImmunoScore Outperforms Conventional Sepsis Tools

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As a biology-based technology company, we combine data science with AI to transform how critical conditions are diagnosed and treated.

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LifeBridge Health deploys Prenosis’ FDA-authorized AI tool to speed sepsis detection

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BioAegis Therapeutics Announces Collaboration with Prenosis to Advance AI-Driven Precision Medicine in Inflammatory Disease

Collaboration aims to identify biological signatures and patient subpopulations most likely to benefit from BioAegis’ recombinant human plasma gelsolin (rhu-pGSN), a novel immune modulator for inflammatory diseases.

NORTH BRUNSWICK, N.J., April 21, 2026 (GLOBE NEWSWIRE) — BioAegis Therapeutics, a pioneering clinical-stage biotech company developing innovative therapies for inflammatory diseases, announces a strategic collaboration with Prenosis®, a leader in biology-driven artificial intelligence solutions for precision medicine, to evaluate biomarkers and patient subpopulations that may demonstrate enhanced response to BioAegis’ gelsolin therapy.

BioAegis’ portfolio is built around plasma gelsolin, a highly conserved and critical immune regulatory protein which rebalances dysfunctional inflammation without suppressing immune function.

Under the collaboration, Prenosis will apply its precision medicine platform to analyze biospecimens and clinical data from BioAegis’ ongoing 600-patient Phase 2 clinical trial, BTI-203, which is evaluating recombinant human plasma gelsolin (rhu-pGSN) for the treatment of moderate-to-severe acute respiratory distress syndrome (ARDS) (NCT05947955), a life-threatening condition characterized by severe lung inflammation and respiratory failure. The goal of the collaboration is to identify biological signatures and patient subgroups that may preferentially benefit from gelsolin therapy, further advancing a precision medicine approach to critical care.

ORIGINALLY PUBLISHED BY BIOAEGIS. READ THE FULL RELEASE >