Member Info for Pingu777

Death spiral CLNs 🤦‍♂️

I'm at a point where I don't think a lot needs to be said any more with HEMO. I'm relaxed and enjoying our progression. The Share Price will catch up. I trust the boss to see this through from here. I'm really exited to see how well it continues to work.

HG CT 1 is the real deal imo. Seems inevitable to me big pharma will want it.

My opinion is that Vlad will have offers before the end of Phase One. Also I've previously said that I can see phase one being shortened with fast track approval from FDA - if patient data continue as it is. In my opinion 9 could be enough for adults. Which would mean 6 more.

HG CT 1 with paediatric trials officially open has now become a very sought after asset. The quicker medium/big pharma move the better the deal they get but the quicker the SP rise investors. The longer it takes, the more patient data we accumulate, the better deal we get and the SP goes higher.

As I've said before, time is on our side.

Can we take the chemo chat elsewhere. HG CT 1 will replace it. Its old news. Toffers deliberately spamming the board. Green bin them please.

Agree sharply. Worked for my mum also.

Look up bone marrow transplants (HSCT) for AML patients. Typical time til transplant from diagnosis of r/r AML.

Then not le patient 1 is already at 7 months+ and p2 3 months+.

As well as replacing chemo HG CT 1 is currently doing well at replacing bone marrow transplant as well.

CDX, initially designed to do the conditioning also treats the AML now, as well as other blood malignancies.

HEMO is designed to replace chemo (apart from the 5 day conditioning pre-dose). That is why it’s so good. Don’t listen to the nonsense.

Https://x.com/nih/status/1973133617778794553?s=46&t=qr0mmBDmB7Vlpu28HK3yMw

You'd imagine there'll be some very interested eyes gazing over HEMO right now and taking note.

I agree. I would think Dr Short is ethically obliged to move things along as swiftly as permitted based on what he knows about HG CT 1.

The progress Hemogenyx have made on their comparatively minuscule budget is nothing short of astounding. The milestones being regularly ticked off by HEMO are substantial. Todays IRB approval to proceed with the paediatric trial and to dose children, Vlad himself confirms its significance in the RNS – and he doesn’t do overplaying anything.

So after only 2 patients safety and early efficacy data MDA deemed it exceptional enough to submit the paperwork to FDA to amend the protocol and add paediatrics. As we know, FDA agreed to this request. MDA have multiple AML trials on the go and I can’t see any other trial they’re involved in expanding to kids.

Truly ground-breaking and astounding stuff and an indication how good (safe and efficacious) HEMO CAR T already looks.

Then you get IRB approval from MD Anderson announced today, the foremost cancer research and treatment centre in the world, to begin the paediatric trial for real. Some kids will be in the hospital at MDA Houston, being cared for as best they can but without any effective treatment to improve their outlook. This approval to proceed after IRB at MDA means that children with very little hope are suddenly going to be thrown a lifeline. A chance at being fixed. I for one think this is truly fantastic.

If Dr Short at MDA was rushing to get the paediatric trial approved so quickly with FDA. If the FDA are happy to sign off the paediatric protocol amendment so early on such limited data. If FDA were happy to sign off the treatment of patient 3 when outside typical protocol granting special permission. Then who is to say Big Pharma are not making early moves now in relation to rushing to secure such an exciting and novel asset?

And yes, it is novel. It is ground-breaking. HG CT 1 has hit so many firsts already on its trial journey it is blazing a trail and maybe it feels too good to be true for observers looking in or the under researched. I personally believe Hemo have a CAR T treatment worth in excess of a billion pounds and only expect the excitement to grow from here.

Agree with SocialistB, seeing Vlad's treatment begin to help more and more people, changing lives, as well as seeing such amazing work drive up the share price of your investment... It doesn't get much better imo.

Good luck all shareholders.

Indeed it’s a huge step for the sick children on the ward at MDA.

This is IRB approval at MDA to begin the trial.

FDA approval is old news. This is permission to practically go and prove its worth a load of cash.

Recruitment will have begun now.

Cracking news. Onwards the big wheels roll.

FDA approved peds expansion ✅

MDA approved peds expansion ✅

Let’s get saving childrens lives. Excellent.

I’m blocking you for being utterly pathetic. I’d rather read Aldes posts than yours. Really.

One again using the word guarantee when no one said. Keep pedalling your lies.

I think it’s more absurd to believe it will not be £18+ in six months personally. And you certainly are an absurd individual.

I’ll get it deleted NotPosting… oh wait… that’s your style ;-)

No one can answer that.

But I can tell you now if you hold HEMO for 6 months you will make a lot of money.

Quite a few posts seem to have disappeared. I wonder why?

Can't wait to get the green light to move forward with the trial. Hopefully it's not too far away.

Green bin Bob working overtime.