News Focus
News Focus
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RobotDroid

09/08/24 9:46 AM

#718787 RE: Guzzi62 #718760

Exactly.
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learningcurve2020

09/08/24 10:11 AM

#718794 RE: Guzzi62 #718760

That's a pattern we see here. Everyone seems to feel helpless because of their fractional ownership percentage because of the massive dilution reflected in shares outstanding. Hmm.
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dennisdave

09/08/24 11:02 AM

#718816 RE: Guzzi62 #718760

DCVax could have been on the market years ago and in different cancers if it wasn't for the management's greed. A powerful partner with money and man power could have moved this quickly forward and applied with the FDA as well.



exactly well said

added to that. Management chose to build a CDMO for the second time with shareholders' money and not to invest in new cancer indication trials and to stay with CRL. And now grifter Powers, at last ASM, dares to BS how proud she is of Toucan's subsidiary Advent
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Investor082

09/08/24 2:02 PM

#718860 RE: Guzzi62 #718760

I agree with you as well. However, you will be disappointed if you are counting on big pharma to get involved in the next year or two. Until recently, I thought big pharma was lurking around as well and thats what was driving their non action around hiring and reimbursements when they are sitting on the cusp of approval in the UK.

But it’s increasingly clear now that no big pharma is interested in this company and management via its social media army will continue to kick the can as usual. First it will be Flaskworks and when that does not go according to plan for another year or two, then the attention will be deflected towards Direct. All this while they can’t even get reimbursement in the UK or approvals from other jurisdictions for L. There will be no support or marketing blitz from the UK media after approval either. These guys just do not have the right skill set, team, and the backing from big players. It should have been clear by now.

For instance, if they did plan on applying to EU or Canada (forget about US) they would have done it by now or would do it as soon as they get UK approval notice. If they cant submit those applications (at least EU and Canada) in 4 years then something is terribly wrong. Forget about reimbursement in any jurisdiction. Why would any investment firm or big pharma treat them seriously if they cant execute in a reasonable way what’s in their control?

I’d watch for these signs and not remain a bagholder when we do get a spike at UK approval because there will be limited to no major milestones for another year or so.