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Contact us with any questions or comments regarding our novel approach to treating infectious, inflammatory, and degenerative diseases with our plasma gelsolin technology platform.

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Stay informed of our latest discoveries and news.

GENERAL NEWS/MEDIA

June 2020: BioAegis Therapeutics Completes Over-Subscribed Financing for COVID-19 Trial

June 24, 2020

June 2020: KYW InDepth Podcast – Why NIH is Studying a NJ Lab’s COVID-19 Treatment?

June 10, 2020

May, 2020: Study of BioAegis’ Lead Product, Gelsolin, is Key Component of NIAID Strategic Plan for COVID-19 Research

May 21, 2020

May, 2020: BioAegis ‘Inflammation Regulator’ Highlighted in CNBC Feature Story on COVID-19

May 11, 2020

Low Admission Plasma Gelsolin Concentrations Identify Community-acquired Pneumonia Patients at High Risk for Severe Outcomes.

Community-Acquired Pneumonia Requiring Hospitalization among U.S. Adults.

Delayed administration of recombinant plasma gelsolin improves survival in a murine model of severe influenza.

Delayed Administration of Recombinant Plasma Gelsolin Improves Survival in a Murine Model of Penicillin-Susceptible and Penicillin-Resistant Pneumococcal Pneumonia.

COMPANY DETAILS

LOCATION:
BioAegis Therapeutics
North Brunswick, NJ

MEDIA INQUIRIES:
Contact: Christine Lagana
clagana@bioaegistx.com

INVESTOR INQUIRIES:
Contact: Steven Cordovano
scordovano@bioaegistx.com

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Our lead product for severe pneumonia, rhu-pGSN, has application for COVID19.