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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 jfm1330on Jan 02, 2022 12:09pm
122 Views
Post# 34277262

RE:RE:RE:Updated time line

RE:RE:RE:Updated time lineAgain, we all knew they were slower than expected in the phase Ia, and now, maybe that reached a higher dose than really expected, or they reached their best case scenario which is three times the MTD of docetaxel alone. All that being said, nothing has changed on the communication timelines. In an article in the Montreal newspaper La Presse on October 13, it is stated this: "Theratechnologies will update the first part of the Phase 1 trial again when it finds the maximum tolerated dose of the drug. Company plans to move to the second part of the Phase 1 trial in the first quarter of 2022"

Again, if it goes in February or March, I expect the company to update the market about it with reitarating that the MTD is not reached yet and telling at what dose they are. I expect it because even though they said they would update when the MTD would be reached, they also always said that it would be, at the latest, at the begining of 2022. So if it is to go beyond that, they should update the market. That being said, I don't expect efficacy data until the end of phase Ia.
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