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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 activated compounds and their associated drug formulations. The Company operates through two divisions: Anti-Cancer Therapy (ACT) and Cool Laser Therapy (CLT). The Anti-Cancer Therapy division develops patented, and patent pending drugs, called Photo Dynamic Compounds (PDCs) and activates them with patent pending laser technology to destroy specifically targeted cancers, bacteria and viruses. The CLT division is responsible for the Company’s medical laser business. The Cool Laser Therapy division designs, develops, manufactures and markets super-pulsed laser technology indicated for the healing of chronic knee pain. The technology has been used off-label for healing numerous nerve, muscle and joint conditions. The Company develops products both internally and using the assistance of specialist external resources.


TSXV:TLT - Post by User

Comment by Eoganachton Apr 26, 2024 3:56pm
242 Views
Post# 36010165

RE:Anktiva comment

RE:Anktiva commentGood post DJDawg

I would just note that the Anktiva CRR at 24 months is already down to 25%. The patients with a CR at 24 months will have received 3 weekly treatments in month 19. Those still CR at 25 months are also eligble for 3 more weekly treatments in each of month 25, 31 and 37.

Like you I am encouraged by Ruvidar PDTs durability of response after 12 months. The most recent swimmer's plot shows that every patient who had a CR at 12 months maintained that response at 15 months. By the end of 2024 the 52 patients who had ther 15 monthy assessment as of the end of March should have reached their 24 month assessment. How well will the 38% CRR at 15 months stand up at 24 months? It's hard to say, but I'm confident it will be much higher than Anktiva's 25% !




DJDawg wrote: Wanted to add in comments to the Anktiva conversation.

The approval process was way longer for this drug because it was biologic. Ruvidar is not so faster assessment process for production process with lower chance of being CRL'd for factory issues. 

While the stats look good for the CR while on the drug, they have not generated stats on longer term CR once done the intensive phase. When TLT gets the longer term data, if it shows that the CR continues to hold then that puts it into the unique category of drugs that don't have steady CR fall off after the first year. I love how all the continuous CR's that go CR from 90 to 360 seem to hold at 450. I feel like that sustained CR is the key to BTD and AA more than anything else.

One other challenge with Anktiva is the tethering to BCG. We know that uro-oncologists are struggling with the supply issues such that a lot of first round patients are under-treated with BCG compared to gold standard. So now we are saying that all those BCG failure patients need to be enrolled back on the BCG supply wagon. For now, where is all this BCG going to come from.

IBRX was smart to market the drug has having potential to work on other cancers but it is not convincing that it would work that well. Bladder is unique. On the other hand TLT has some great data on how versatlile their compound library may be.

So all in all, I'm just waiting, as we all do here. I do hope that the next patient update includes some extended results on the CR as we go further out. They don't have enough/any new patients to impact the 90 day CR numbers at this point.

GLTA





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