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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 May 03, 2024 8:39am
121 Views
Post# 36021228

RE:RE:RE:RE:RE:RE:RE:RE:RE:RE:RE:POC in humans has been acheived is that it

RE:RE:RE:RE:RE:RE:RE:RE:RE:RE:RE:POC in humans has been acheived is that it

To me it seems like they are trying to link the new optimized dosing and its results with previous trial/trial's results. There is still a part 4 for this new trial design. Could they alter it again and go straight to phase2 based on sufficient data? I believe so!




Mannequin wrote:

It seems to me that maybe they have seen something but really have not been able to properly isolate the dose and they are fine tuning it. Is this number of patients enough to get into a Ph2


scarlet1967 wrote:

 

 

Just wanted to clarify the fact that 300mg/m2 is the higher dose level in part 3 of phase1(the second group of the patients will be dosed at that level)! Therefore what ever this new presentation will be revealing almost will be relevant as the dosage is (despite the different intervals, weekly versus previously every 3 weeks) similar to the ongoing clinical trial. 

"The amended study will be a modified 6+6 design with two different dosing regimens that are within the efficacious range for sudocetaxel zendusortide: 1.75 mg/kg on days 1, 8, and 15 of a 28-day cycle (similar to 210 mg/m2 every 3 weeks) and 2.5 mg/kg on the same schedule (similar to 300 mg/m2 every 3 weeks)."

Hopefully with this more frequently dosing they will be better off in terms of both safety and efficacy of the drug.


 


 

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