Wednesday, August 11, 2021 5:18:19 PM
2. I don't see an EUA no matter who says what on this board. We've been over this, and a dosed-60 patient cohort straight to EUA would be ludicrous. IPIX has no manufacturing/distribution/sales etc to meet EUA requirements. (been over this as well)... people are screaming about the vaccines not 'being safe' (even on this board) yet they've been in literally hundreds of millions of humans... 60 dosed people with B? Are you f*king kidding me?
3. Note: IPIX is a PO box run by an accountant and his clinical trials assistant. NOT a swiss BioTech. Relief Therapeutics is run by business people with post-grad business degrees, PhD's etc. They're serious. They're getting things done and going places. Not a fair comparison. NNVC might be a more appropriate comparison I think?
4. Nothing this company has *ever* done in its history has been expedient (except dilution, and payment to The Accountant).
5. There will be no in-house P3 from IPIX without significant outside assistance (grants/partnerships/license etc). There's no current funding to do this and the existing finance agreement isn't large enough to support a P3, to my knowledge, unless the SP magically (and unprecedentedly) went to $5/s. (If it cost $6M to dose 60 people, imagine the cost for 350-500 humans?)
Please let this IPIX nightmare end.
Recent IPIX News
- Form 8-K - Current report • Edgar (US Regulatory) • 02/01/2024 01:30:25 PM
- Form 8-K - Current report • Edgar (US Regulatory) • 12/05/2023 09:25:58 PM
- Form 10-Q - Quarterly report [Sections 13 or 15(d)] • Edgar (US Regulatory) • 11/20/2023 09:05:44 PM
- Form NT 10-Q - Notification of inability to timely file Form 10-Q or 10-QSB • Edgar (US Regulatory) • 11/15/2023 01:00:19 PM
- Form 8-K - Current report • Edgar (US Regulatory) • 10/30/2023 08:15:25 PM
- Form 10-K - Annual report [Section 13 and 15(d), not S-K Item 405] • Edgar (US Regulatory) • 09/28/2023 01:00:08 PM
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