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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

Post by SPCEO1on Jan 20, 2022 5:50pm
301 Views
Post# 34339889

RP2D

RP2DThe RP2D, or recommended phase 2 dosage, is one step below the MTD. So, the 300mg dosage level, or about 1.5x the normal docetaxel dose seems to be the early leader for the RP2D. The higher the dosage level TH can use in phase 1b and phase 2, the better the chances of success. In the pre-clinical charts, the best results were gleaned when the dosage of TH-1902 was a little more than 2x that of docetaxel. So, ideally, the 420mg level would be the RP2D.

Does anyone have any idea why TH does not want to share more specific information on the number of patients dosed at 420mg, whether this is the second time at this level and exactly how long it now looks like it will take them to complete the trial. JFM was ironically suggesting the summer for the trial's end earlier but that could turn out to be correct. 

I really do not understand why TH management has allowed us to be so confused about these basic matters. They already have a credibility problem and these delays are not helping fix that.  
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