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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 Wino115on Sep 07, 2022 6:48pm
159 Views
Post# 34948154

RE:RE:Bicycle Therap. - encouraging in ovarian

RE:RE:Bicycle Therap. - encouraging in ovarianOnce again, helpful posts from you all and further's our understandings of various issues.  As a follow-up, I see that one analyst increased their price target by $10, which equates to $300mil in additional market cap, on Bicycle.  So that's what fairly thin, but decent, data can get you for one cancer indication - a $300mil bump in valuation.

They decreased the discount rate and justified it with these points, some of which apply to TH1902:

 - an 18 month PR (actually quite a good result) and 1 PR in a 12th line heavily pre-treated patient.  But still, just 2 out of 9 results are what the analyst points to.

- going against all statistical rules, they are exicted in urothelial that 2 out of 3 responded, so they think it will have a high ORR and estimate in the 40% range.  Seems silly to base a forecast on such a small dataset.  They were both PRs and one patient had failed Padcev.  So also points out a patient that failed existing SOC, but shows even a PR is a highly positive sign.  We had one of those examples given in the 1a data.

- the dosage safety with few grade 3 AEs and only 1 dose intertuption patient. It sounds like other drugs that targeted EphA2 had a lot of safety issues.  This is one area we need to be cautious about since we don't have any prior datasets of a sort1+ targeted therapy.  We just don't know the full set of issues that may pop up targeting it yet. 

They have first year revenues from this drug in both cancers around $45mil and starting in 2025. They have peak revenues for those 2 cancers of around $300mil for third line treatment, peaking 2030.

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