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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 PWIB123on Oct 14, 2022 3:05am
189 Views
Post# 35024127

RE:Finally listened to call

RE:Finally listened to callYou and Scarlett picked up on the ssame thing I did after I listened to the call myself. It was around the 35 min mark where the lady filling in for Ed Nash started asking questions about the basket trial and when we could expect information on data to be shared.  I thought Christian's comments were extremely positive and provided insight into what his true thoughts were and the best and worse case timelines.  He said he believes we will see signs of eficacy in some (plural) of those tumor types.  He reiterated they are looking for 2 responses or more in at least 1 tumor type.  He said they expect to be able to announce signs of efficacy by end of quarter, and then he backed up and said at least by end of first quarter next year, wihtin next 90 days.  Christian was as direct and confident as anyone could expect.  I thought this was hugely positive!

I also picked up on Paul making a statement that they were seeing a shift in the industry toward administration of Trogarzo in pharmacies rather than clinics and that the IMF push would benefit there.

I thought the team expressed additional confidence in Egrifta being a viable solution in spite of not being an easy to administer pill.  

All in all, while not overly energetic, I thought the call was mostly postured with positive overtones.  I still wanted more, and Paul and the board have got to accept the fact that they have to communicate differently in the future, but I didn't walk away thinking TH-1902 was a dud and the program would be scrapped.  It's just a long-time in the making of what will be an overnight success story.  Hopefully they build on it.

qwerty22 wrote:

I was going on people reaction here before.

I thought the call was fine apart from no ongoing trial update.

There was one nugget when Christian seems to suggest that all the main cancers in the trial had over 85% Sortilin expression. He seemed to suggest that was what the up and coming microarray poster would say. If that's true then that is great, in fact fantastic. The worry that they are enrolling significant SORT- patients is really off the table now. It also makes screening for Sortilin less of a priority for now. That's great news.

The other good point for me is Christian clear said the protocol going forward is see two responders from upto 10 patients, expand to 25 and then move forward to the next phase if they have the data to support that. 

They obviously made a prior decision not to discuss the ongoing trial. My take is it is hitting that 2 responders from 10 that triggers the next update especially if that triggers a quick expansion to 25. So this is what we should be expecting. Should that have happened by now? I don't think so necessarily. If no one cancer type has aggressively enrolled then they could have a mish mash of results where none of those quite reach that go signal benchmark. I guess we have to accept they aren't going to dribble out results on every responder leading up to that point.

I can sort of even understand why they don't want to talk about enrolment rates. If you say it's slow, then that's a negative. If you say it's fast and aren't releasing details on responders then it looks like the drug is a dud.

I think the one conclusion we can say is the probably haven't hit the go signal yet. I'm not too bothered (yet) about the trial being a dud. I'm putting this down to our expectations being too high about was is possible yet. You sort of have to admire their discipline is saying nothing about the ongoing trial. It sucks but they clearly decided to say nothing and they did it well.

On other things. I thought they contextualized the NASH situation the way I understand it. I also thought they inspired a bit more hope that the Trogarzo management plan could yield some potential benefits (eventually). 



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