Monday, August 02, 2021 10:28:08 AM
I think we can do better at the CEO position than someone who steals and lies. That is a non starter for me. Some folks do not have as high an ethical standard as I do for leaders.
It looks like the 13 D effort has not been successful and the market is none too pleased.
I disagree with your Unequivocal opinion. After all, your assessment merely belongs to you and no objective measures were cited in support of same. It is moot at this point.
Assuming FDA was going to play hardball with CYDY’s submission to begin with, Nader was the not an ideal character to shepherd the BLA through the process, given his lack of pharma skills, communication issues and lack of attention to detail.
With the back drop of the RTF and FDA rebuke these characteristics will be negative force multipliers for the BLA re-submission. FDA will be all over the resubmission with a fine tooth comb and that does not bode well for a Nader led submission. Can any successful Nader submission to government bodies be identified? Note: FDA said CYDY needs to learn how to properly craft trial designs.
Now the agenda is revealed and opinions evolve with no rational case for the conclusion. Hatred for Nader is pretty easy to evoke. He lies, steals and has epically failed in his efforts to commercialize LL. The group as coalesced around the desperate need to get a qualified CEO before it is too late.
I have made a pretty crystal clear case, based on the record, that it is improbable for one man to be competent and have epically failed to the degree of Nader unless these failures are purposeful.
The record shows his failures and character, these are not opinions. Cash and time are running out.
It looks like the 13 D effort has not been successful and the market is none too pleased.
I disagree with your Unequivocal opinion. After all, your assessment merely belongs to you and no objective measures were cited in support of same. It is moot at this point.
Assuming FDA was going to play hardball with CYDY’s submission to begin with, Nader was the not an ideal character to shepherd the BLA through the process, given his lack of pharma skills, communication issues and lack of attention to detail.
With the back drop of the RTF and FDA rebuke these characteristics will be negative force multipliers for the BLA re-submission. FDA will be all over the resubmission with a fine tooth comb and that does not bode well for a Nader led submission. Can any successful Nader submission to government bodies be identified? Note: FDA said CYDY needs to learn how to properly craft trial designs.
Now the agenda is revealed and opinions evolve with no rational case for the conclusion. Hatred for Nader is pretty easy to evoke. He lies, steals and has epically failed in his efforts to commercialize LL. The group as coalesced around the desperate need to get a qualified CEO before it is too late.
I have made a pretty crystal clear case, based on the record, that it is improbable for one man to be competent and have epically failed to the degree of Nader unless these failures are purposeful.
The record shows his failures and character, these are not opinions. Cash and time are running out.
3X
God Bless America!
Recent CYDY News
- CNS Drug Delivery Breakthroughs Unlock Significant Biotech Market Opportunities • InvestorsHub NewsWire • 05/11/2026 01:00:00 PM
- CNS Drug Delivery Breakthroughs Unlock Significant Biotech Market Opportunities • GlobeNewswire Inc. • 05/11/2026 12:30:00 PM
- Form 8-K - Current report • Edgar (US Regulatory) • 04/30/2026 08:32:50 PM
- CytoDyn Announces First Patient Dosed in Expanded Access Program for Leronlimab in Triple-Negative Breast Cancer • GlobeNewswire Inc. • 04/27/2026 12:30:00 PM
- CytoDyn to Host Investor Webcast • GlobeNewswire Inc. • 04/23/2026 12:30:00 PM
- Form S-1 - General form for registration of securities under the Securities Act of 1933 • Edgar (US Regulatory) • 04/22/2026 09:21:50 PM
- CytoDyn Presents New Leronlimab Data in Metastatic Colorectal Cancer at AACR Annual Meeting 2026 • GlobeNewswire Inc. • 04/22/2026 12:30:00 PM
- CytoDyn Completes Enrollment in Phase 2 Metastatic Colorectal Cancer Study • GlobeNewswire Inc. • 04/21/2026 08:10:00 PM
- CytoDyn Presents New Leronlimab Data in Metastatic Triple-Negative Breast Cancer at AACR Annual Meeting 2026 • GlobeNewswire Inc. • 04/20/2026 12:30:00 PM
- CytoDyn to Present at the AACR Annual Meeting 2026 • GlobeNewswire Inc. • 04/14/2026 12:30:00 PM
- Form 424B3 - Prospectus [Rule 424(b)(3)] • Edgar (US Regulatory) • 04/08/2026 09:15:18 PM
- Form 10-Q - Quarterly report [Sections 13 or 15(d)] • Edgar (US Regulatory) • 04/08/2026 12:30:28 PM
- Form 424B3 - Prospectus [Rule 424(b)(3)] • Edgar (US Regulatory) • 03/25/2026 09:16:10 PM
- Form 4 - Statement of changes in beneficial ownership of securities • Edgar (US Regulatory) • 03/24/2026 09:24:23 PM
- Form 4 - Statement of changes in beneficial ownership of securities • Edgar (US Regulatory) • 03/24/2026 09:23:14 PM
- Form 4 - Statement of changes in beneficial ownership of securities • Edgar (US Regulatory) • 03/24/2026 09:22:42 PM
- Form 4 - Statement of changes in beneficial ownership of securities • Edgar (US Regulatory) • 03/24/2026 09:21:33 PM
- Form 4 - Statement of changes in beneficial ownership of securities • Edgar (US Regulatory) • 03/24/2026 09:20:57 PM
- Form 4 - Statement of changes in beneficial ownership of securities • Edgar (US Regulatory) • 03/24/2026 09:20:20 PM
- Form 8-K - Current report • Edgar (US Regulatory) • 03/24/2026 09:15:24 PM
- CytoDyn Presents at AACR Special Conference in Cancer Research: Brain Cancer • GlobeNewswire Inc. • 03/24/2026 12:30:00 PM
- Form 424B3 - Prospectus [Rule 424(b)(3)] • Edgar (US Regulatory) • 03/09/2026 09:15:18 PM
- Form 8-K - Current report • Edgar (US Regulatory) • 03/05/2026 01:35:02 PM
- CytoDyn Closes $17.5 Million Financing to Fund Continued Development of Leronlimab • GlobeNewswire Inc. • 03/05/2026 01:30:00 PM
- CytoDyn Presents Novel CCR5 Inhibition Mechanisms and Long-Term Survival Signals for Leronlimab in Metastatic Breast Cancer at AACR Immuno-Oncology Conference • GlobeNewswire Inc. • 02/20/2026 01:30:00 PM
