A clinical study of Leronlimab in patients for the treatment of COVID-2019 infections in critically ill population

Status: Planning

Phase of Trial: Phase II

Latest Information Update: 07 Apr 2022

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30 Mar 2022 According to a CytoDyn media release, the U.S. Food and Drug Administration (FDA) a full clinical hold on leronlimab its COVID-19 program in the United States. Under the full clinical hold on the COVID-19 program, no new clinical studies may be initiated until the clinical hold is resolved.
11 Mar 2021 New trial record
08 Mar 2021 According to a CytoDyn media release, the Company anticipates the Health Canada Interim Order (IO) could allow the Company to sell leronlimab in Canada, while additional critical COVID-19 patients are enrolled. These discussions are on going, and the Company has initiated the process to submit an IO with Health Canada.

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