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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 scarlet1967on Jul 01, 2021 3:31pm
106 Views
Post# 33479856

RE:RE:RE:RE:RE:RE:RE:RE:RE:RE:RE:RE:RE:Fitting

RE:RE:RE:RE:RE:RE:RE:RE:RE:RE:RE:RE:RE:FittingThe dose escalation can take longer as they will be dosing a single patient during the first two cycles until DLT is shown if not they keep dosing therefore they  add more levels of dosing to the program so essentially they could end up with more cycles but I believe the cut off for the MTD will be at 560mg/m2 therefore the MTD can't be three times more than Docetaxel as per company their PDC at 230mg/m2 is equal to 100mg/m2 of docetaxel which is the therapeutic dosage for Docetaxel.
At best it will be a bit over twice the docetaxel's safe and therapeutic level which is a great result.
There is no valid reason to increase the dosage past those levels it will not only expose group of patients to unnecessary high dosage increaseing the risk for toxicity during phase 1 but also throughout the remaining phases.

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