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Quantum BioPharma Ltd C.QNTM

Alternate Symbol(s):  QNTM

Quantum BioPharma Ltd. is a Canada-based biopharmaceutical company. The Company is engaged in building a portfolio of assets and biotech solutions for the treatment of challenging neurodegenerative and metabolic disorders and alcohol misuse disorders with drug candidates in different stages of development. Through its wholly owned subsidiary, Lucid Psycheceuticals Inc. (Lucid), it is focused on the research and development of its lead compound, Lucid-MS, which is a patented new chemical entity to prevent and reverse myelin degradation, the underlying mechanism of multiple sclerosis. Its unbuzzd beverage is a proprietary formulation of vitamins and minerals to help with liver and brain function for the purposes of relieving the effects of alcohol consumption and restoring a normal lifestyle. It maintains a portfolio of strategic investments through its wholly owned subsidiary, FSD Strategic Investments Inc., which represents loans secured by residential or commercial property.


CSE:QNTM - Post by User

Bullboard Posts
Comment by JAKPUG4LIFEon Apr 16, 2020 1:36pm
128 Views
Post# 30917445

RE:RE:RE:RE:RE:RE:RE:RE:FSD Pharma Inc Timeline

RE:RE:RE:RE:RE:RE:RE:RE:FSD Pharma Inc TimelineGraham, These boys will always duck direct questions. I assume visionary is another one from the facebook group, more than likely a second account with a regular like rosenberg(24k). Still waiting on the investors, how many weeks into Nasdaq now?No volume, more mis- information on the trials. More options for the big boys. Seems like wce is another one we can add to the see you later list. GLTA
GrahamB wrote:
TheVisionary202 wrote:
There is nothing different Phase 2 's rundown is phase 2 A and B lol you make it sound like Phase 2 and phase 2 A and B is a seperate category lol its all the same thing

Phase 2 starts after Good Data from Phase 1 in australia

I know you want FSD Pharma to fail but they will succeed and haters will hate even more once they succeed because they will all look like fools lol


Visionist, you demonstrate a lack of knowledge about options and clinical trial design and the NDA via FDA.
 

(And you continue to duck direct questions)

 

That is fine to lack knowledge-but most serious learners  don’t continue to defend themselves and dig a deeper hole with more misconceptions and further errors.
(Errors in logic with investing bias hurt over time)

 

The point is-they did promote an accelerated program of phase 2/3-they are now on a timeline which is relatively slow, and with caveats in funding and depletion of working capital, in my view.

 

Here is a link to an article educate you on the accelerated path, and combined with the previous FDA link, will hopefully help you learn about the process.

As a long, it would be helpful to understand the process.
You will have to understand it yourself-

Have a good day-see ya.

 

https://www.jstor.org/stable/27590571?seq=1



Bullboard Posts