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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

Post by DJDawgon Oct 20, 2023 4:11pm
400 Views
Post# 35693749

update on stats in relation to FDA advisory panel

update on stats in relation to FDA advisory panel
The FDA panel from way back indicated support for a drug that could achieve:

- 40%-50% at 6 months (note that they don't list 3m CR or CR at any time)
- 30% for 18-24 months, with the lower bound of the 95% confidence interval excluding 20%

UPDATED FROM OCT 16 NEWS RELEASE
The statistical angle is where it gets tricky. My math says for 95% confidence interval we are at:
Total group (optimized and non-optimized)
3m: 45-71%
6m: 43-69% (NOW meet this one on the lower bound, whereas not quite before)
12m: 21-50.6%
15m: 17.9-48% (not quite 20% on the lower bound since for the margin of error for 42 patients is plus or minus 15.13%)

The only thing holding back the 15 m data from looking better is that the smaller the sample size, the wider the error margins are.

My hunch is that when the pre-BTD review was looking at data, the probably asked for 18m data on the patients as the FDA panel listed 18m as the wish list from way back. This would mean contacting the centres and asking for updates on the patients in question.
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