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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. 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. Its portfolio includes Phase I clinical trial of sudocetaxel zendusortide (TH1902), a novel peptide-drug conjugate (PDC), in patients with advanced ovarian cancer.


TSX:TH - Post by User

Comment by SPCEO1on Dec 02, 2022 3:33pm
209 Views
Post# 35147441

RE:RE:RE:RE:Not surprising

RE:RE:RE:RE:Not surprisingYou said "And now with lower and more frequent dosing, they will aim more at stable diseases than clear objective responses that would allow a fast approval."

Based on what I have heard the company said, this is not what THTX is thnking. It seems they got some mild responses and are looking to tweek the dosing approach and the targeted cancers as wel as the relative health of the patients to get a better response rate. They do not seem very interested in stabilizing the patient's cancer but rather are aiming for a significant impact. So, they are altering the dosing in such a way as to actually get moreTH-1902 into the body than previously by using more frequent dosing of smaller amounts, they are targeting a narrower range of cancers where they believe the hit rate will be more in their favor and are seeking somewhat healthier patients than have taken the drug so far. It sounds like they have learned a thing or two about which patients may not respond well based on previous therapies they have taken and will seek to avoid those.

My impression is they will be putting the new protocol together with the assistance of the trial investigators so hopefully that helps with recruitment once they start up again as the investigators will have been part of the solution. Apparently, another peptide drug conjugate company did similiar alterations to their trial and got better results.

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