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CytoDyn Submits Protocol with the FDA for Phase 3 Registrational Trial of Leronlimab for Critically

During recent discussions with the FDA, the agency suggested that developing leronlimab for critically ill COVID-19 patients in current situation in U.S. appears feasibleVANCOUVER, Washington--(BUSINESS WIRE)--CytoDyn Inc. (OTCQB: CYDY) (โ€œCytoDynโ€ or the โ€œCompanyโ€), a late-stage biotechnology company developing lero...
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