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Sesen getting added to Russell 3000 index. I’ll take it.
Agreed. Need to see action, IF the intent is even there.
No sir, respectfully, double check the link and read carefully. This has been mistaken a lot I’ve seen. It’s 100 million DOLLARS worth of shares (currently about 25-30 million additional shares at current price). Up to a fully diluted OS just over 200 mil (currently at approx 170mil outstanding).
In Palmer we trust, lol. Well done sir.
Legggo!
Do I hear tree fiddy come close Tuesday
$3 is being a real pain in the ass
Fully support that idea.
July it is! Hoorah! Lol. Thanks bud
Cmon MM’s take her all the way south of a penny PLEASE. Would love to 5X my holdings and average down.
In your talks did he hint at when he might follow up on the tweet?
Eyal is the CFO.
https://protalix.com/about/management/
Just cuz +200MM shares passed, that doesn’t mean we are guaranteed to see them all issued/used.
Will the OS go up with time, yea until this is approved. Is it better than traditional debt financing for a non-revenue generating company, absolutely. Is it better than convertible debt, very much yes.
Who the F is getting 130k traded??
Tick tock
New research report from hamman partners last week. Near term 1.56/sh CAD (1.27/sh USD). Potential acquisition value 8.16/sh CAD (6.64/sh USD)!!!!
Posted on black iron website under research reports. Gaining traction!
Criminal really
What a giant crock of shit from the FDA. Give them an F- for not doing their jobs.
Think you’re correct, which isn’t that what balance is for?
Protalix Bio says FDA rejection for PRX–102 was not due to safety/ efficacy issues
Apr. 28, 2021 2:29 PM ETProtalix BioTherapeutics, Inc. (PLX)
By: Dulan Lokuwithana, SA News Editor
Giving further updates on the FDA rejection of its experimental therapy pegunigalsidase alfa (PRX–102) for Fabry disease, Protalix BioTherapeutics (PLX -37.6%) says that the regulator has not cited any safety or efficacy concerns in the Complete Response Letter ("CRL").
The inspection of the company’s Protalix's manufacturing facility in Carmiel, Israel was required for the approval of the marketing application along with a subsequent assessment of findings, the FDA has said.
But the regulator was unable to inspect the site on time due to COVID-related restrictions on travel.
As for the third-party fill and finish facility in Europe for PRX-102, the FDA has said it will communicate any outstanding issues to the manufacturer.
The regulator has also highlighted the full approval granted for Fabrazyme, a development Protalix will have to consider in any resubmission of the accelerated approval for PRX–102.
The company is planning to request a Type-A meeting with the FDA.
PRX–102 achieved study outcome in the BRIGHT study which involved 30 patients with Fabry disease previously treated with enzyme replacement therapy (NASDAQ:ERT) (agalsidase alfa – Replagal or agalsidase beta – Fabrazyme).
Ok who is playing with the price....
It’s still listed in the pipeline I thought
Thought you said it was ludicrous for them to be working behind the scenes? Lol, cmon bud I can’t keep up.
I do agree with VC, we aren’t out of the woods and as I’ve said before, I’m not saying they will put out a release, I just believe that- backed by other comms by other posters- they MAY truly be working behind the scenes and don’t want to put out too much fluff to risk getting in SEC trouble.
Just curious if you meant CTDT specific tweets? Our co has not deleted any tweets. The one just posted about OCMillionaire was in regards to that person pumping $ARCS.
That should read "aka @OCmillionaire" https://t.co/fIZzGIcwLS
— George Sharp - Advocate for truth in the OTC (@GeorgeASharp) March 15, 2021
What tweets?
I’ve chalked this up to an L if/when I can sell the lot. It was surprising to even see an active tweet. Could be a suprise to all of us
Very well could be. Not reading too much into it, but to me drafting and posting a tweet gives credence to what others have posted about communications saying something is happening behind the scenes. We’ve waited this long why not a little longer, heck it.
Seems like the really don’t care about the AS increase
Agreed. I dunno when and to what extent but we asked for a pulse (outside of the few here who have semi regular correspondence from Saunders saying they’re working on it). The tweet was at very least a pulse.
I can’t see why waste the time to draft a tweet saying something is coming after all this time of silence, if nothing is indeed coming. Seems completely counter intuitive to me.
It’s unfortunate but *hopefully* this gets remedied soon before SEC cracks down
Surely it has to be of significant substance to take the time to tweet anything after this long of nothing.
I’d hope it’s:
-Chill remedied
-Current on everything
-Patents protected
-Machine working and calibrations completed
From CTDT twitter account posted right now:
“We've been quiet throughout a period of great change and upheaval, Management has been developing and finalizing a complete restructuring of The Company and believe that shareholders should see a significant increase in value. We expect to make a formal press release soon.”
We've been quiet throughout a period of great change and upheaval, Management has been developing and finalizing a complete restructuring of The Company and believe that shareholders should see a significant increase in value. We expect to make a formal press release soon.
— Centaurus Diamond Technologies (@CentaurusCtdt) March 11, 2021
Anywhere from $5-250 depending on the source lol
I’m excited to hear that one
I’ll agree the atm doesn’t help anything but capital needs, I’m a little more concerned about overall market forces at this point. Not to cry wolf, but let’s say nasdaq drops to 11k soon. We could see high $1s low $2s, i would think, due to the drag of the prevailing market.
Yea I think that expected. They have the ATM in place which has been running/amended twice now (maybe 3 times). I expect fully diluted to be ~175-200mil shares when it’s all done.
Saying got added?
Where are you seeing these Form T’s