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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 Jul 20, 2021 9:52pm
131 Views
Post# 33579698

RE:RE:RE:TH2101

RE:RE:RE:TH2101I forgot this was the cytotoxic agent in the Immunomedic ADC, even though I saw it was very potent. Now, as the codename suggests, they have this molecule since January of this year, so they likely already have some animal data with it. Now, if Thera can come with a clear proof of concept with TH1902, the then they come out with spectacular animal data with with TH2101. 1+1=2. It would really strongly push forward the idea that they have a platform able to generate multiple PDCs aiming at an extraordinary target which is sortilin. Some PDCs that will likely be better than TH1902, also, down the road, PDCs that could be used in combo therapies. That's why the proof of concept is so important.


Wino115 wrote:

This would also really help but parameters around the program and and u Delhi get possible valuation metric.  Certainly narrows that unknown future value that we and the market don't quite have a handle on now.  Putting that comp up there makes it really easy for analysts to justify rather large values.

 

Wino115 wrote:

 

This is strategically very ballsy!  I haven't been able to read the new deck,  but this is potentially huge.   The reason?  That cytotoxic is what is on the ADC Immunomedics created that was bought by Gilead for $21bil. And we know its name -Trodelvy.  This would be the Trodelvy killer!

So the industry and FDA gushed over the Trodelvy science for mTNBC and it was approved after a brief P3 reading backed up the P2 data.  But the toxin escapes and ends up in the digestive tract causing bad nausea and diarrhea. I believe the FDA sent back some of their early science trials because of that.  So if this concentrates the drug in the tumor better with less effllux and better safety, it will crush Trodelvy.  Absolutely kill it on day 1.   Gilead needs $5bil+ annual revenue to justify their $21bil price tag.  No way if this works.

This would prove up the entire platform for THTX and get AApproval for each program.  So what do you pay for a platform that works on way more than one cancer type and with many CYTO toxins?  Far more than $21bil in my book and I hope the BOD knows that!
 

jfm1330 wrote: On new information in the updated corporate presentation is the identity of a new PDC made out of TH19P01. It was given the codename TH2101, which likely mean it was the first research molecule made by Thera in 2021, jusy my guess. That being said, they also revealed with is the cytotoxic drud that is attached to TH19P01, and it is a molecule called SN38, which is the active metabolite of a drug called Irinotecan. This is a topoisomerase I inhibitor and it is 1000 times more active than irinotecan.

https://en.wikipedia.org/wiki/SN-38

 

 





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