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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) (“CytoDyn” or the “Company”), a late-stage biotechnology company developing lero. ....

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Predictors of partial immunization among children

Despite the increase in global immunization coverage, however, many children around the world, especially in developing countries, are still left unvaccinated. ....

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