Cytodyn Inc (CYDY): FDA very impressed with Leronlimab. The...

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Tuesday, 10/06/2020 9:30:03 AM

Tuesday, October 06, 2020 9:30:03 AM

FDA very impressed with Leronlimab. The very reason they suspended EIND patients is we were taking on so many 60+ it was creating A lot of paperwork and they want trial to be approved and finished as much as shareholders do It saves lives and it’s less work for them if they approve the only drug that reduced mortality.

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Recent CYDY News

Form 8-K - Current report • Edgar (US Regulatory) • 06/03/2024 09:15:10 PM
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Form 424B3 - Prospectus [Rule 424(b)(3)] • Edgar (US Regulatory) • 05/06/2024 09:16:24 PM
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Form 3 - Initial statement of beneficial ownership of securities • Edgar (US Regulatory) • 02/16/2024 02:00:24 AM
Form SC 13G/A - Statement of acquisition of beneficial ownership by individuals: [Amend] • Edgar (US Regulatory) • 02/12/2024 10:31:57 PM
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Form 8-K - Current report • Edgar (US Regulatory) • 01/29/2024 01:40:14 PM
Form 424B3 - Prospectus [Rule 424(b)(3)] • Edgar (US Regulatory) • 01/19/2024 10:15:35 PM
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Form 4 - Statement of changes in beneficial ownership of securities • Edgar (US Regulatory) • 01/06/2024 02:04:57 AM
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