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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 jicoopon Apr 05, 2022 2:20pm
207 Views
Post# 34577635

RE:RE:The 23 Optimized Patients

RE:RE:The 23 Optimized PatientsHey enrique , I see the tables are confusing quite a few today . I tried earlier to decipher mathematically, and welcome others to do so as well. The first table ( non optimised ) shows 25% CR Evaluated at 450 days out, which I beleive is 5 out of 20 reaching that milestone. The second table only shows 1 out of 9 hitting 450 days with a CR Evaluated of 11.1 % .  Thusly, we cannot get to the numbers for CR at 450 days that you have suggested below ,as I've highligthed. I thin it will be in the 15 to 20% range . Correct me if you think I'm wrong .

Coop

enriquesuave wrote:

Sounds very precise Eoganacht.  Of the 4 Nonresponders at 90 days, that includes 1 patient who passed away before 90 days assessment and had a high  chance of being CR given this patient had a negative urine cytology at 30 days.  Technically speaking results should be out of 22 patients, and 4 who only got a second Optimized dose should be counted separately IMo.  Results are impressive, not 100% CR, but still impressive given the novelty of a One and Done treatment ( plus a One and Done Maintenance treatment at 6 months).  Far better than any single agent I've seen and with way less treatments and side effects.  For sure we still need more data to finalize the numbers, but I can easily see 65% or even 70-80% CR at 90 days with with around 35-45% CR at 15 months.  A potential New Gold Standard in the making.All IMO

 

Eoganacht wrote: I think I finally understand the data for the optimized patients. If I got anything wrong please correct me.

In the last newsletter there were 18 patients who had received an optimized treatment.

The 90 day data for those 18 patients was as follows:

44% CR (8 patients)
11% partial response (2 patients)
39% pending (7 patients)
6% no response (1 patient) 

We were waiting to find out what happened to those 7 pending patients. Would they also be CR at 90 days? Since then 5 more patients have been treated so now there are 23 patients with an optimized treatment and since there are now 3 patients pending, 2 of the 5 reached 90 days so there are 9 more patients at the 90 day mark than there were at the time of the last newsletter. Here are the results for the 23 optimized patients.

The 90 day data for the current 23 optimized patients is as follows:

52.2%
CR (12 patients)
17.4% partial response (4 patients)
13 % pending (3 patients)
The news release does not explicitly tell us how many non-responders there were, but 23-19=4 therefore:
17% no response (4 patients)

Of the 9 patients who reached 90 days since the last report 
44%
CR (4 patients)
22% partial response (2 patients)
33% no response (3 patients)

As the news release makes explicit there is still the potential of 82.6 CR at 90 days for the 23 optimized patients (52.2% CR + 17.4% PR + 13% pending)
 

 

 



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