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Pfizer lowering PPS via SEC investigation preparing for a BO :p can always dream huh?
Good CC, things are looking good.
Announcing that they sold for a few millions' worth of venom would be a nice, unexpected event :)
If they produce 5 gallons a year they must have a few by now ;)
Im happy with what the management accomplished n not even a year, personally.
Cancelling the right to RS gave me the impression that they were directly responding to our concerns, showing us they care for us shareholders.
I only wish we would be able to show as much confidence in them with the PPS, but our time will come! :)
GO QNTA!
Hahahaha quality paint takes longer:p
Well they have said in that last PR that they were awaiting approval by FINRA for a symbol change.
That satisfied me, not sure what else you are expecting? Copy of a USB key with all e-mails/phone calls about FINRA?
Haha in all seriousness though I believe they feel like us about it like : "its coming anyday now, no need to put out a useless PR" Then 2 weeks later : "Guys I tell you its coming its been TWO WEEKS! We gonna release PR then get it next day OF COURSE.. just add a paragraph in next awesome news we get"
Atleast that's my take on whats going on in their offices :p
Is QNTA starting to behave? :o
YOU GO QNTA! :)
That would be the perfect complement to the OTCQB uplist :)
Totally agree with your post.
Only thing you seem to be overlooking is the willingness of DR govt to include Escozine into its COVID treatment program ASAP. When they released tgat PR (about 2 weeks ago), the ministry of health VP said she would put together a commitee to figure out the roll out of Escozine.
I am thinking due to the seriousness of Covid situation in the DR that this won't take months, and an update on that, which would be reflected in earnings too, could do a great deal to not only propel our PPS in the right direction, but so to minimize the amount of dilution that could possibly xome our way.
Whatever the case, gotta put your sunglasses on to look at QNTA's future.. sun is shining :)
Closing my eyes and opening them only when I smell money, and it IS coming ;)
FAITH. ITS NOT ONLY ABOUT RELIGION! :D
Hope you grabbed 'em today cause I don't think we're headed that way. SORRY!
GETTING CLOSE NOW FOLKS!
Been sitting on it for close to a year now, TIME TO GET PAID ! :)
So happy with the shares I bought yesterday :)
Finally a bullish day, not just a spike on open then big red all day haha :)
Whatever, know what you hold eh?
Avg'd all the way down to .0312 today LOL! :)
GGC identifies new gold and VMS targets for phase 2 drilling and reports on phase 1 drilling at Normetal.
https://www.newsfilecorp.com/release/101046
25% position increase at 0.025 :)
Let's not forget the DR about to order Escozine for the country! They were setting up a committee ASAP to figure this out, so I'm thinking we're gonna have a nice surprise in the "accounts receivable" section of next earnings :)
Diafor drilling is doing the drilling for GGC as we speak
I think you guys know the way out. Thank you :)
Annual report + attorney letter
https://www.otcmarkets.com/stock/APYP/news/video?v&id=424
We got some green atleast! :)
BUCKLE UP FELLAS! :))
INSIDER INFO next Q financials gonna have atleast 180$ inflow :) I fell for the discounts on Aelia store :p
Anxiously awaiting drilling results. So promising!
Free extra marketing hurraaah hahaha
They cancelled their right to RS. Very unlikely lol
Hopefully tomorrow we gain some momentum! :)
I want to buy those pens to complete my QNTA merch collection lol
I found this company selling IMMUNA PEN made with scorpion venom, from 2020.
Don't seem active but had Anyone seen that before?
https://www.instagram.com/unikarx/?hl=en
I don't think it is fake. And I sure hope it's not. But I can't say with 100% certainty that it is legit. Yet.
They still sell products on amazon, so the technology and company must exist.
But I never saw the immunapen anywhere, nor the DR PSA, or the polarization machines, and now this company. I'm still bullish but clarifications on a few points would be great.
"The company has hired an advertising agency to help with the rollout of the new branding expected second quarter 2021. This will work in conjunction with a major push the company is on the path of with some major big box retail chains. "
Exactly what I was saying Jedi..
Thanks Samuel for bringing up the person I was refering to.
They do have marketing professionals. And these people hired Tony Hawk. And created a whole new brand. In the last month. How many marketing teams do you want?
I believe they are doing a great job, considering we don't have our new ticker yet. Why advertise everywhere a stock that's gonna be renamed?
Because of new DNA protocols. This is forward. Not backwards.
If FDA is negative, I'll be selling a few other stocks to buy the resulting dip for sure!
Exciting times ahead for sure! The calm before the FREAKING HURRICANE!!
From what I read, they will be able to use clinical trials in the DR for their FDA submissions. Is it only for the IND though or other trials too?
Makes me feel like things will be happening at a very fast pace once they have that IND designation.
"While our near-term goal is to work with the Ministry of Environment of The Dominican Republic to bring this drug to market, we are able to use this data in our programmes around the world, including with our submissions to the US Food and Drug Administration."
https://www.clinicaltrialsarena.com/news/medolife-rx-positive-data-covid-19-drug-candidate-study/
"(b) As sole basis for marketing approval. An application based solely on foreign clinical data meeting U.S. criteria for marketing approval may be approved if: (1) The foreign data are applicable to the U.S. population and U.S. medical practice; (2) the studies have been performed by clinical investigators of recognized competence; and (3) the data may be considered valid without the need for an on-site inspection by FDA or, if FDA considers such an inspection to be necessary, FDA is able to validate the data through an on-site inspection or other appropriate means. Failure of an application to meet any of these criteria will result in the application not being approvable based on the foreign data alone. FDA will apply this policy in a flexible manner according to the nature of the drug and the data being considered.
(c) Consultation between FDA and applicants. Applicants are encouraged to meet with agency officials in a "presubmission" meeting when approval based solely on foreign data will be sought."
https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfcfr/cfrsearch.cfm?fr=314.106
Fact that they have met with agency officials, even though they already have people that are experienced with the FDA, makes me think that they will indeed try to seek approval based solely on their DR trials :) Which have been goooood
DEAR STOCKGOD, ALLOW QNTA TO PLEASE US WITH POSITIVE NEWS FROM THE IND!!! THANKUCOMAGAIN
MEDO is my guess!