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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 Aug 20, 2021 1:48pm
138 Views
Post# 33740529

RE:RE:RE:RE:RE:RE:RE:NASH in the ATM Prospectus

RE:RE:RE:RE:RE:RE:RE:NASH in the ATM ProspectusLooking at comps, you could justify $200mil given how they got there. But a stock market could give +/- 50% around that as we've seen.  I don't think there's really a lot in the current THTX valuation for that asset.  Maybe $50-75 mil if I still use my $100-150mil oncology option value.   It's all guesswork, but I don't think we can ascribe the same kind of value we see others imputing to some of the other NASH assets.  

qwerty22 wrote:

I think you value them as strongly entering 2b or a risky shot at a registrational trial. I think there is certainty about that uncertainty because they went through the Ph3 regulatory process and at a minimum the fda said they were registrationally ready (with some caveats).

What would you value that asset in the depressed NASH market? $300 mil? More?

I think this is what going through the fda process and completing it gives them, it sets a baseline on the value of the program based on the FDA's decision making process rather than difficult to understand concepts like 'the totality of the data'. Hopefully a partner appreciates that, eventually when/if the program gets started then the market will appreciate it too.




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