Member Info for Chris0123

What I do know is that if we do get non-dilutive funding, someone is going to get caught very short on the aptly named poop deck. GLA

We all know the risks in investing in potentially life saving treatments. High risk high reward and potentially winning patients too. However, we don't need our noses rubbed in it every time there is a hurdle to jump. This is the frustration with disguised shorters. They pretend they are there to help guide you as to the perceived difficulties but at the same time create an environment of even greater uncertainty within the people they purport to guide. Trust yourself. GLA

The Interactive Investor interview which JHFH posted is worth a few listens, not least because it comes from the key players in Hemogenyx. I think, as a few have suggested, there was the omission of comment on funding and we could read different things into that. However, Peter Redmond offered up "ready to move forward now at apace" without prompt or hesitation. It leans more toward the view that finance to do so does not seem to be a worry, "at a pace" he said. The fact that we have not heard anything is causing angst in some quarters but I think talks are ongoing and I also think that if you believe in the scientific developments , JV type funding will undoubtedly come. Of course, we all hope sooner rather than later GLA

Well well well! What a mad mad week. I have been away and have just now caught up with activity at Hemogenyx and the posting over the same period. Monk's Scream & Dante's Inferno quickly spring to mind. Very hard to see the wood for the trees with the insult threads and that's without DogFarther whom I blocked weeks ago. I just could not decipher his content.

When the sp doesn't do what an investor thinks it should do, all hell is breaking loose EVEN WHEN the scientific progress is astounding. The SP will follow good science not bad science. Funding will come, the Board of Diectors are not stupid it has to come and they know it has to come on good terms to allow the science to bear fruit otherwise not even they will win let alone the patients. Let's all contribute to this BB in a way that contains some professionalism and dignity. For those not invested, you have no right to be toxic with anyone anyway. Put up or shut up I say. Jeepers the science is going brilliantly big investors will follow. GLA

Brilliant find! The author should have written the RNS. GLA

Not a bad SP considering we've had fire, pestilence, famine,flood, a plague of locus and a nuclear war today...GLA we'll be OK I think.

Sorry Saint!!!

There are so many possible interpretations. I would hope that Dr Sandler would not be so crass as to state "....I won" and then burn investors with news that would crash the sp in the same breath. He's a shareholder if he wins, we win.

Would hazard a guess something will be communicated tomorrow and he has been completely vague at to the subject matter such as not to draw scorn from regulators. The variations in interpretations tonight support this. Although "looking forward to and overcoming the next challenge" suggests he doesn't know what that challenge is. If not CAR T Phase 1 success he's moved on to CBR and has the funding to do that by licensing CAR T. Just musings, don't hang me. The morning may reveal all because his post tonight is more than about clinical consent, that's out as news already. GLA

Haywain, really great to have the benefit of your expertise on this board. Certainly helps cut out the scientific noise and misinformation. By improving investor understanding we become more invested in the company and what it can potentially achieve. Although I am kind of glad you are not charging for the privilege. Roll-on Monday.

I would have thought that Dr S would have been a little less restrained on X with regard to today's news. Correct me if I have missed something, but I would have expected some comment on this milestone other than simply the RNS text. I deduce from that, that he couldn't rather that wouldn't given the milestone he has reached. "Couldn't" because of an impending RNS on Monday most likely funding in some form by a partner organised and ready to go. We're he in need of a Bob or too still, he or Prevail would have been out there today hitting the media and putting out the PR which would have been primed and ready to kick into action between resubmission and today's approval. The silence today suggests to me they were happy to sit through Friday and will probably announce partnership funding by Prevail or like Prevail. GLA (Gheko all the best to you and family)

Hi IslandGirl...Poster Haywain is a great scientific source you should read his posts.

He has dealt with this question a lot to educate us but also to deal with less scrupulous posters seeking to diminish the inique work Hemo are engaged in. GL

The day started like a wedding celebration. Guests (posters) known and ounknown. Everyone smiling at the start of the day. There for a common reason, in this case to celebrate the next phase in Hemo's life. As the day progresses and the drink flows you mingle and mix and there are those guests you would hardly wish to see again when the day is over. There were others who made unnecessary t*ts of themselves and you hope never to come across them again. However, many maintained absolute dignity and calm despite what was served up on the day left you somewhat cold. They remembered why they were there though which was to celebrate a stage in a life (going clinical) and understanding developing and growing is not defined by the results of one day.

Hemo are clinical stage , the FDA consented as expected but it could have been so much worse. Can the last guest to leave tonight turn of the lights, the cleaners will be in to mop up and Monday we start afresh as a clinical stage company.

It has landed guys!

With you on that one Dhub

If Asleep works for the FDA we are all toast!!!

An ill-researched comment at best and a spurious one at worst Dr Deo. However, the seasoned and well-researched PI's have swiftly & roundly dealt with it. GLA

Wake up Asleep! Get with the programme.

Asleep - if you agree a plan with the FDA and successfully test the solution and resubmit I think that should put us in your 10% (even if that was a reliable source). The FDA can't set Hemo in motion on a half-baked plan and then come up with something else to hold it back.

I don't know about anyone else but I am on tenterhooks. The CH lift predictions suggested a more swift response and even though I am just 1 day and a bit from my own prediction, I am a little surprised that the FDA haven't turned this around within the last week or so. I maintain comfort in the fact that whilst it was not a quick "yes", it wasn't a quick "no" either. In addition, how many times have you asked someone for feedback on a proposal several weeks in and the response is typically "Oh I will get a look at that in the next day or so, promise!"... perhaps this resubmission is one they are not too worried about (they have agreed a plan) and will actually deal with it within the last 15 days not the first 15. . GLA

Thanks JHFH, now we are back on track!!!!