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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

Comment by wildbird1on Sep 21, 2022 8:56am
308 Views
Post# 34975885

RE:63% still have their bladder at 270 days...

RE:63% still have their bladder at 270 days...For those who ask, what would the TR% look like if we were to replace the 12 undertreated patients with 12 optimized patients?

The answer is in the 3Q2021 Newsletter(page 5).
TLT said "In summary, for patients who received the primary optimized Study 11 Treatment, there is a 5% increase in CR and a 75% decrease in NR".
The 75% decrease in NR(Non Responder) will end up in the TR(CR+PR) numbers.

Quick math..the answer is approximately +70%TR, that +70%TR is important because when the time will come for TLT to negotiate a deal with a big pharma, it will be the +70%TR numbers that will be used by TLT to negotiate the $value of a deal.

At this point in time it is the data that matter, not the SP, focus on the data and let the manipulation play with the SP, let them have fun for now, it's ok(they play with a very low numbers of shares).

When the time is ripe(Dec 2022), the data will confirm the 450 days TR% efficacy, and the SP will react accordingly.

+70%TR, for patients that were 100% guaranteed to lose their bladder, try to place a $value on this...

Christmas time is coming, and it is going to be great.


wildbird1 wrote: Let's try to understand why TLT is including a TR(CR+PR) line in their data.

Google "Cancer Partial Response & Partial Remission" and you will find 3 interesting facts.

1) "Partial Response" mean the same thing as "Partial Remission".

2) For some patients Partial Response (Partial Remission) can last a lifetime.

3) If you are a PR patient, you can take a break from treatment, and keep your Bladder.
In this linkhttps://webmd.com/cancer/remission-what-does-it-mean
It said " Partial Remission means the cancer is still there, but your tumor has gotten smaller (usually 30 to 50% smaller). If you are in Partial Remission, it may mean you can take a break from treatment as long as the cancer doesn't begin to grow again".

If you can take a break from treatment, it does mean you will also keep your bladder as long as you are a PR patient(could be for the rest of your life).

Let's take a look at the 270 days data.
Note 1) didn't use the 360&450 day data because we don't know how many Optimized patient are included in the 360&450 days data, versus 18 verifiable Optimized patients at 270 days.
Pressrelease Aug 29,2022.
270 days data (including 18 Optimized patients).
CR...........................13  patients.......41%
PR.............................7  patients.......22%
TR(CR+PR).............20 patients.......63%
The above mean that 63% of patients still have their bladder at 270 days.

Not bad considering this....The category of patients that the FDA gave to TLT for treatments didn't respond to any available treatments, and these patients were 100% guaranteed to lose their bladder.
For these patients, Partial Response(in Remission) is a huge relief.

Keep in mind that the 63%TR at 270 days include the 12 undertreated patients(the FDA know this).
Note: In Dec 2022, 18 Optimized patients will have completed their 450 days data, the current 33%TR will definitively be much higher.

The more you understand the data, the more you realize that the FDA BTD approval in Dec 2022, is in the bag.






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