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Theratechnologies Inc T.TH

Alternate Symbol(s):  THTX

Theratechnologies Inc. is a Canada-based clinical-stage biopharmaceutical company. The Company is focused on the development and commercialization of therapies addressing unmet medical needs. It markets prescription products for people with human immunodeficiency viruses (HIV) in the United States. The Company's research pipeline focuses on specialized therapies addressing unmet medical needs in HIV, nonalcoholic steatohepatitis (NASH) and oncology. Its medicines include Trogarzo and EGRIFTA SV (tesamorelin for injection). Trogarzo (ibalizumab-uiyk) injection is a long-acting monoclonal antibody which binds to domain 2 of the CD4 T cell receptors. It blocks viral entry into host cells while preserving normal immunologic function. The Company is also investigating an intramuscular method of administration of Trogarzo. EGRIFTA SV (tesamorelin for injection) is approved in the United States for the reduction of excess abdominal fat in people with HIV who have lipodystrophy.


TSX:TH - Post by User

Comment by SPCEO1on Mar 23, 2022 8:06am
76 Views
Post# 34536912

RE:A few reminders from the KOL event a while back

RE:A few reminders from the KOL event a while backTo sum up what I think Wino was saying here, if you are making your decisions because of your emotional reaction to a falling share price rather than based on the science, you are doing it wrong. Stock prices rise and fall based on a myriad of factors which impact the supply and demand for the shares in the short term. Those factors often have nothing to do with the fundamental position of the company. As Buffett says, in the short term the market is a voting machine in the long term it is a weighing machine. This too shall pass since the science has a lot of weight.
Wino115 wrote: 1. Ovary tumor total accumulation in healthy vs. tumor cells (Rubicin v. TH1904)
For TH1904 the tumor cells accumulated 8000 ng/g of tissue
For TH1904 the healthy cells accumulated 300 ng/g of tissue

For plain Rubicin, tumor cells accumulated 1000ng/g of tissue
For plain Rubicin, healthy cells accumulated 1200ng/g of tissue.

Which means sort1 as a target pulled in a lot of the dose and very little appeared in healthy tissue. Both went in the right direction --more in tumor, less in healthy - especially compared to control of IV rubicin.


2. Half life of sort1 is 4 minutes, half life of TH1902 is 1 hour.  So in 2 hours, it's all out.
For an ADC, it takes 6 to 10 hours to get it all out.


3. Off target accumulation. Marsolais pointed out that the control is an IV of a chemo that goes into essentially every cell in your body with no targeting at all; hence, the safety issues.  Sort1 is the only protein they know of that increases a lot with the severity of the cancer progression, so for the patients they are targeting, it will be by definition very high.  His quote on the off target is that sort1 normally is not very highly expressed (as seen in the healthy tissue stain samples), and given this, the half life, and the PDC approach the concentration in other cells expressing sort1 would be "...very, very low".  Obviously, this is all in vivo he's talking about. Did mention it will not cross the blood brain barrier. When you listen back on it, you are reminded that the important factor is not necessarily a massive dose of chemo, but the ability to be far safer and quickly concentrate it in as many sort1 expressed cells quickly, thus reducing side effects and allowing patient to get another dose quickly and keep going. Did mention that for any of the cancers that are typically not detected early (lung, ovary), targeting sort1 may be best option.


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