Join today and have your say! It’s FREE!

Become a member today, It's free!

We will not release or resell your information to third parties without your permission.
Please Try Again
{{ error }}
By providing my email, I consent to receiving investment related electronic messages from Stockhouse.

or

Sign In

Please Try Again
{{ error }}
Password Hint : {{passwordHint}}
Forgot Password?

or

Please Try Again {{ error }}

Send my password

SUCCESS
An email was sent with password retrieval instructions. Please go to the link in the email message to retrieve your password.

Become a member today, It's free!

We will not release or resell your information to third parties without your permission.
Quote  |  Bullboard  |  News  |  Opinion  |  Profile  |  Peers  |  Filings  |  Financials  |  Options  |  Price History  |  Ratios  |  Ownership  |  Insiders  |  Valuation

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

Post by Wino115on Jun 13, 2023 11:16am
159 Views
Post# 35493693

Investigators, very helpful - lots to digest

Investigators, very helpful - lots to digestHaving the KOLs was highly beneficial --realistic, reminder of clinical benefit equation, placing actual results into the context of their practices and what they see. Fascinating that someone who has discontinued is still seeing stability --that is worth trying to understand and I can only think it has something to do with disrupting the CSC and VM part.  There's a lot to unpack, but I don't think these KOLs thing the program is dead, it stumbled and they think there are answers given they saw PRs and lots of SDs. They seemed to also point that SDs of 3-6 months is a winner for these last stage patients where there appears to be no real solutions on offer from the ADC side. 

Qwerty's right that the main issue for them is the neuropathy. They seemed to say that, while more data would be needed, they don't think it's because of the sort1 expression around the nervous system, but the accumulated amount of "free docetaxol" that is at issue. Yet they were very clear they think dosing and timing has worked in the past at "controling" this (Winer said it).  I don't know enough, but are they saying the one huge dose may leave more "free" taxol buzzing around doing bad things and that if they do smaller doses it always be a lower dose, not accumulate in the body as much, allow the receptors to get occupied and then recycled to cell surface, and they hope that will lower it to a tolerable level?  Clearly will be there, they just want to get it tolerable for what they see as the novel benefit -- allowing people to take this for a long, long time. Marsolais pointed to at least one patient where the neuropathy was likely because the surface area vs weight dosing gave the patient that 420+ type dose which caused the known problems they saw previously.  

All in -- loads of information to digest, actually very good questions from the analysts and attendees, candid responses from KOLs.   Need to rewatch and get the finer points.  Look forward to other's views here, but I can see why they think this is a "way forward", but as the KOLs kept repeating, it must show  that clinical benefit --the simple equation of confirmed benefits outweighing adverse events. I think they also dispelled the need to do Sort1 testing pre-treatment and pointed out no ADC did that, they all just picked cancers known to have a lot of the target.  They did seem to place the overexpression of Sort1 as being high (Dr Winer) and it seemed he meant more prevalent than what he's seen in other targeted therapies. 
<< Previous
Bullboard Posts
Next >>