Tevogen said it is accelerating its Biotech and Digital Health verticals to move investigational TVGN 489 into its next clinical phase. Tevogen cited proof-of-concept data showing 100% of treated high-risk patients did not develop Long COVID. The company said identifying five additional HLA targets expanded potential eligibility for TVGN 489 to about 65% of the U.S. population. Tevogen also said it is evaluating the acquisition of Sciometrix and its Clinicus platform for real-world monitoring and data collection in future trials.
Disclaimer: This news brief was created by Public Technologies (PUBT) using generative artificial intelligence. While PUBT strives to provide accurate and timely information, this AI-generated content is for informational purposes only and should not be interpreted as financial, investment, or legal advice. Tevogen Bio Holdings Inc. published the original content used to generate this news brief via GlobeNewswire (Ref. ID: 202603111515PRIMZONEFULLFEED9670301) on March 11, 2026, and is solely responsible for the information contained therein.
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