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Pharmala Biotech Holdings Inc C.MDMA

Alternate Symbol(s):  MDXXF

PharmAla Biotech Holdings Inc. is a Canada-based biotechnology company. The Company is focused on the development, manufacture and sales of methylenedioxy methamphetamine (MDMA) and methylenedioxy phenethylamines (MDXX) class molecules in service to the burgeoning clinical research community and growing commercial use cases in select jurisdictions. The Company has three primary business lines: the manufacture of MDMA and MDXX class molecules for sale to clinical researchers in both the commercial and academic sphere, the research and development of novel MDXX class compounds which offer unique benefits above and beyond known substances, and the development of novel delivery mechanisms for MDMA and MDXX class compounds. Its research and development unit has completed proof-of-concept research into several IP families, including ALA-002, its lead drug candidate. It works with laboratories across Canada to develop novel processes for the supply of LaNeo MDMA and other MDXX substances.


CSE:MDMA - Post by User

Comment by inviolablspiriton Aug 12, 2024 10:30am
65 Views
Post# 36174393

RE:Pharmala's US patent granted for ALA-002

RE:Pharmala's US patent granted for ALA-002 The Market cap of this company doesn't make much sense at these prices with their IP and business proceeding in Australia and Canada which hasn't changed when it traded at over 30 cents.

Nick has said time and time again that an FDA approval would have given Lykos exclusivity to the US market for 5 years and so Pharmala's focus is in Europe and South America.  And he has said that it can be very expensive to break into the US market with new drugs so it has never been their focus. However, the company can now look at supplying clinical trials in the US market with LaNeo MDMA if they choose to for additional revenue.   To an extent this is good news for Pharmala.  Lykos' loss is Pharmala's gain.

Again, their focus is moving into the European and South American markets.  A much smarter move, which has not changed.  Those markets were always on their own path regardless of what the FDA decided in the US.  Nick's focus has always been correctly focused on the best markets to enter for the least cost to the company.  This comes with his knowledge and experience of understanding regulations.  Eventually they will work their way into the US with their new drugs.

ALA-002 intrigues me the most because it could eventually get ophan designation status for increasing social interactions for those with autism spectrum disorder.  This type of drug would be the first of its kind and any treatment use may also recieve it own data exclusity period by the FDA as well.  interesting times ahead with FDA approved patent now in hand.
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