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Tevogen Bio to Study its Investigational COVID-19 T Cell Therapy in Immunocompromised Patients Who a

Tevogen’s investigational precision T cell product, TVGN-489, is a genetically unmodified, off-the-shelf, allogeneic cytotoxic CD8+ T lymphocyte (CTL) product with activity against multiple precise targets across the entire SARS-CoV-2 genome.The immunocompromised COVID-19 patients who are unable to take or unlikely...

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Tevogen Bio to Study its Investigational COVID-19 T Cell Therapy in Immunocompromised Patients Who are Unable to Benefit From Currently Available Prevention or Treatment Options

Tevogen Bio to Study its Investigational COVID-19 T Cell Therapy in Immunocompromised Patients Who are Unable to Benefit From Currently Available Prevention or Treatment Options
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Tevogen Bio Announces Positive Safety Results Upon Completion of Patient Enrollment in Proof-of-Concept Clinical Trial of T cell Therapy for Elderly or High-Risk COVID-19 Patients

Tevogen Bio Announces Positive Safety Results Upon Completion of Patient Enrollment in Proof-of-Concept Clinical Trial of T cell Therapy for Elderly or High-Risk COVID-19 Patients
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Tevogen Bio Announces Positive Safety Results Upon Completion of Patient Enrollment in Proof-of-Conc

No dose-limiting toxicities or significant treatment-related adverse events were observed for any patient at any dose levelWARREN, N.J.--(BUSINESS WIRE)--#COVID19--Tevogen Bio, a late stage clinical biotechnology company specializing in the development of cell and gene therapies in oncology, neurology, and virology,...

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Pennsylvania
United-states
Philadelphia
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Tevogen Bio Initiates Final Dose Level in Proof-of-Concept Clinical Trial of its Investigational T c

Trial has advanced to the fourth and final dose escalation cohort with no dose-limiting toxicities observed to-dateTevogen’s investigational T cell product is genetically unmodified and target-specificThe enrollment is expected to conclude in the second quarter of 2022WARREN, N.J.--(BUSINESS WIRE)--Tevogen Bio, a la...

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Tevogen Bio Announces Positive Safety Data from Second Cohort in Ongoing Proof-of-Concept Clinical T

- No dose-limiting toxicities reported in first or second cohorts (n=6)- The dosing of patients on dose levels one and two marks the midway point of the trial’s planned four dosing levels- All patients in the second cohort infected with Omicron variant as opposed to the first cohort of patients who were infected wit...

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