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CytoDyn Inc completes submission of all major sections of CMC to FDA for HIV Biologics License Application

This CMC is a critical part of the biotech s Biologics License Application (BLA) for HIV - the request for permission to commercialize a product ....

Nitya Ray , Nader Pourhassan , Chris Recknor , Cytodyn Inc , Food Drug Administration , Drug Administration , Biologics License Application ,

CytoDyn Inc. reveals 'very strong' updated results for cancer patients receiving its flagship drug leronlimab

A 12-month analysis of 28 metastatic triple-negative breast cancer patients receiving leronlimab suggests an increase of 3,600% in 12-month. ....

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CytoDyn Reports Preliminary Results from First Five Patients in Phase 2 NASH Open Label ...

Press release content from Globe Newswire. The AP news staff was not involved in its creation. ....

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Senhwa Presents Positive Initial Data from Phase 2 Clinical Trial of Silmitasertib (CX-4945) in Moderate COVID-19 Patients At the ISIRV-WHO Conference

Statistically significant 133% faster time to COVID-19 clinical symptoms recovery versus standard of care (SOC)/best supportive care. Statistically significant. ....

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CytoDyn Receives Clearance from Brazil's ANVISA to Commence Phase 3 Trial for Severe COVID-19 Patients | Business

CytoDyn Receives Clearance from Brazil's ANVISA to Commence Phase 3 Trial for Severe COVID-19 Patients | Business
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