Monday, October 16, 2017 10:15:29 AM
And it is that interim, the one expected in the summer of 2015 (coincident with the FDA clinical hold) where I am suggesting futility was observed on PFS.
Avii, how did the FDA find out about this futility result on the 2nd IA if the co never released it and kept it secret according to you? So why the hold again? I am not familiar with the broad history of futility recommendations in the past, but I strongly suspect that they did not always get a hold response from the FDA if the co decided to continue with the trial.
First, let's be clear. It is the first efficacy interim analysis at 60% of 248 events in the summer of 2015 that we are talking about. (not the 2nd IA).
How did the FDA find out? A requirement of the IND is to provide updates to the FDA on the status of the trial.
Recall the recent Cel-Sci clinical hold.
In their 8k disclosing the hold they say:
"In its partial clinical hold letter, FDA identified the following specific deficiencies: a) FDA stated that there is an unreasonable and significant risk of illness or injury to human subjects and cited among other things the absence of prompt reports by us to the FDA of IDMC recommendations to close the study entirely (made in spring of 2014) or at least to close it to accrual of new patients (made in spring of 2016);...."
https://www.sec.gov/Archives/edgar/data/725363/000165495416005085/cvm_8k.htm
So, there is an example showing that the FDA insists on being notified of important DMC rec's.
and, futility was an issue there:
"FDA furthermore stated that the study is unlikely to demonstrate that the addition of our investigational drug Multikine to the standard of care is superior to standard of care and thus should be terminated for futility;"
So, if you read the link above you will see a fairly detailed disclosure of their hold. It would seem this full disclosure to shareholders is the norm rather than the exception. I would acknowledge that the lack of a similar full disclosure for NWBO's hold is evidence against my theory (evidence, not proof). Why would every other company disclose details about their hold and NWBO keep silent?
I believe the answer, in part, relates to rule 10b-5. Disclose all or nothing. NWBO choose nothing. And their lack of communication is part of the reason this is trading at 17 cents.
Finally,
and kept it secret according to you?
I never said the company kept anything secret from the FDA.
Recent NWBO News
- Form POS AM - Post-Effective amendments for registration statement • Edgar (US Regulatory) • 04/16/2026 09:25:30 PM
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- Form 8-K - Current report • Edgar (US Regulatory) • 01/15/2026 10:06:20 PM
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- Form DEF 14A - Other definitive proxy statements • Edgar (US Regulatory) • 11/28/2025 09:43:27 PM
- Form EFFECT - Notice of Effectiveness • Edgar (US Regulatory) • 11/26/2025 05:15:34 AM
- Form 424B5 - Prospectus [Rule 424(b)(5)] • Edgar (US Regulatory) • 11/25/2025 10:23:07 PM
- Form 8-K - Current report • Edgar (US Regulatory) • 11/20/2025 09:26:03 PM
- Form PRE 14A - Other preliminary proxy statements • Edgar (US Regulatory) • 11/19/2025 09:15:48 PM
- Form 10-Q - Quarterly report [Sections 13 or 15(d)] • Edgar (US Regulatory) • 11/14/2025 09:44:21 PM
- Form 8-K - Current report • Edgar (US Regulatory) • 10/31/2025 04:29:10 PM
- Form 8-K - Current report • Edgar (US Regulatory) • 10/30/2025 08:40:05 PM
- Form 8-K - Current report • Edgar (US Regulatory) • 10/24/2025 04:28:38 PM
- Form 8-K - Current report • Edgar (US Regulatory) • 10/14/2025 06:22:26 PM
- Form 10-Q - Quarterly report [Sections 13 or 15(d)] • Edgar (US Regulatory) • 08/14/2025 09:00:38 PM
- Form 424B5 - Prospectus [Rule 424(b)(5)] • Edgar (US Regulatory) • 07/01/2025 09:04:38 PM
