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Tuesday, November 03, 2020 5:22:25 PM
does a company usually PR or 8k an IND submission?
has there been any clarity on the 30 day wait period post filing an ind before starting a trial?
does a company normally specify the trial start date and hospitals involved?
has anyone heard if gmu is moving forward with in vivo testing?
is there an update on the inhaled version of brilacidin as a prophylactic?
add on studies? IPIX annouced they will have excess B for C IV dosing for additional studies. When would we hear about that?
GMU mentioned in their pre-print that the B for C IV could be studied as a 3 in 1 (not sure if just limited to coronoavirus)
there is a lot of juice to get ipix up over the previous high in the .60's if not above the dollar mark. would love to do something similar to cytodyn that went over a buck, then based around 3 bucks before charging to 10. No one would have ever imagined it could get that high with their s/s.
the above is all IMHO (consider this my safe harbor statement)
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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