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Posted On: 08/19/2020 1:26:22 AM
Post# of 148903
CytoDyn Requests “Fast Track Approval” for COVID-19 Patients from U.K.’s Regulatory Agency MHRA based on its Top-line Report Showing Statistically Significant Endpoint, NEWS2 (p < 0.023) and Notable Safety Results
https://www.cytodyn.com/newsroom/press-releas...r-covid-19
https://www.cytodyn.com/newsroom/press-releas...r-covid-19
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