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Theralase Technologies Inc. V.TLT

Alternate Symbol(s):  TLTFF | V.TLT.W

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 N0taP00pon Apr 05, 2023 4:20pm
1046 Views
Post# 35381842

Range of CR at 450 day mark

Range of CR at 450 day markNot clear if they will use the data as-is from the ASCO poster to submit a request for BTD, in which case 450 day CR stands at 28% (8 of 29) as stated.  There were 3 IRs waiting to be re-categorized at the 450 day mark…and 4 more left to move from 360 day to 450 day mark (2 were CRs, 2 were IRs).  Total of 7 additional data points.   ASSUMING they were waiting for those 4 patients (from 360 day) to move into the 450 day slot AND assuming they ALL happened in Q1, then, best case would be all 4+3  are CR (15 total CRs  at 450 day mark meaning ~ 40% CR@450).  Worst case would be none of the 7 were CR which means 8 total CRs remains as-is at 450 day mark….which is ~22% CR@450).   The real results are likely to be somewhere in between ie 22% to 40%. Still better than Keytruda.  I didn’t exactly score high in math, so could be way off.  It all depends on when they filed, or plan to file. It also depends on how the FDA reads the data and evaluations. GLTA. 
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