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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

Comment by DavidRosenbergon Feb 22, 2023 1:41pm
80 Views
Post# 35298821

RE:Biotech analysis criteria run through

RE:Biotech analysis criteria run throughThey failed covid trials with 1 patient tested  = raza bokhari leadership he was ceo 

cannabis venture failed = Thomas fairfull leadership he was the ceo of FV Pharma 

lucid acquisition was done by none of the previous leadership roles now it's on current management to grow value 

current management and leadership with real updates

phase 2 trials currently recruitment for FSD PEA and mast cells idiopathic pain green light with 60 patients total with a mast cell diagnosis 
 Health Canada green light for lucid MS trials this tests healthy subjects 

Phase 1 and Phase 2 trials are two stages of the clinical trial process for testing the safety and efficacy of new drugs or therapies. Here are the main differences between the two phases:
 
Purpose: Phase 1 trials are primarily focused on assessing the safety of the new drug or therapy, determining the appropriate dose range, and identifying any potential side effects. Phase 2 trials are designed to evaluate the drug or therapy's effectiveness in treating the targeted condition and to further assess safety.
Participants: Phase 1 trials typically involve a small number of healthy volunteers (typically fewer than 100 participants) who are closely monitored for safety and potential side effects. Phase 2 trials involve a larger number of participants (usually between 100 and 300) who have the condition the drug or therapy is intended to treat.
Duration: Phase 1 trials are generally shorter in duration, typically lasting a few months, while Phase 2 trials may take several months to a few years.
Endpoints: In Phase 1 trials, the main endpoint is typically safety and tolerability, while in Phase 2 trials, the primary endpoint is often the drug or therapy's effectiveness in treating the targeted condition.
Design: Phase 1 trials are usually designed as single-arm studies, with all participants receiving the new drug or therapy. In contrast, Phase 2 trials may be designed as randomized, controlled trials, where some participants receive the new drug or therapy and others receive a placebo or standard treatment.
Overall, while both Phase 1 and Phase 2 trials are important stages in the clinical trial process, they serve different purposes and involve different types of participants and study designs.

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