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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 jfm1330on Mar 02, 2022 3:16pm
130 Views
Post# 34476291

RE:RE:RE:RE:RE:RE:RE:RE:RE:RE:Very difficult to be constructive

RE:RE:RE:RE:RE:RE:RE:RE:RE:RE:Very difficult to be constructiveThey said that they tested many patients with multiple doses at 420 mg/m2 and these patients were likely treated at 300 mg/m2 before that. I understand phase Ia is not designed to show efficacy in the best possible way, that being said, given they know which cancer are very likely to overexpress sortilin, it is hard to believe that out of all that not a single patient will show some tumor shrinkage. If the concept behind TH1902 is valid, there has to be at least one or two patients showing some signs of efficacy. Likely it will not be the full efficacy of the drug given at the right dose for 6 cycles or more, but at least there has to be some signs. If there is absolutely no signs of efficacy in any patients, it will be very worrisome.


jeffm34 wrote:

What results are you expecting from the the phase 1a?  The only results they will announce will be the dose they are using in the phase 1b trial.  They've already said that will be 300mg barring any major change in findings. 

 

SPCEO1 wrote: Obviously, the timing is hard too as we should be hearing about the phase 1a results right around the time of the AGM

 

 

 



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