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Theralase Technologies Inc. V.TLT

Alternate Symbol(s):  TLTFF

Theralase Technologies Inc. is a Canada-based clinical stage pharmaceutical company. The Company is engaged in the research and development of light, radiation, sound and/or drug-activated small molecule compounds, their associated drug formulations and the light systems that activate them, with a primary objective of efficacy and a secondary objective of safety in the destruction of various cancers, bacteria and viruses. It operates through two divisions: the Drug Division and the Device Division. The Drug Division is responsible for the research and development of light-activated small molecules primarily for the treatment of cancer with assistance from the Device Division to develop medical lasers to activate them. The Device Division is responsible for the Company’s medical laser business, which research, develops, manufactures and distributes cool laser therapy (CLT) systems to healthcare practitioners, predominantly for the healing of pain.


TSXV:TLT - Post by User

Post by BullCall2262on Jan 07, 2025 8:50am
311 Views
Post# 36392027

Followed Stockhouse for a long time, but never made an acct

Followed Stockhouse for a long time, but never made an acct
 
Been in this stock since 2017. Their most recent Pre-BTD application was submitted in early October 2024. The FDA has 60 days to review and did, which left them with a recent response in early December 2024. Assuming the data they wanted to see was there and the only reason they didn't accept it, must have been some sort of formatting issue. That said, the Pre-BTD was then submitted just a few days later in December roughly between the 1st and the 8th (can't recall the exact date). The FDA has 60 days from that date which puts us right around Feb 8th timeframe to see if the data was presented correctly. In my opinion, the only reason to re-submit the Pre-BTD application only days later means they FDA was good with the data and just wanted to see it presented in a different format. What's next? The company would apply for formal "Break Through Designation" (BTD) and the FDA has 60 days to respond to that. It is a tedious process, but I believe if the Pre-BTD is accepted, you will start to see real money flow into this stock and it could get pushed into the low dollars quickly. The company stated that they are targeting 2027 for the approval of the drug, so it's still a few years away from that, but someone should partner up with them when the price is low to accelerate this process. It is a long process, but I would say we should see a significant stock movement within the next 3 months. This is my opinion, but good luck to all.
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