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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 Jun 28, 2021 3:54pm
150 Views
Post# 33460938

RE:RE:RE:Where things are at

RE:RE:RE:Where things are atThey already published that in IND enabling toxicity study they were able to give three times the maximum tolerable dose of free docetaxel. We don't know how it will translate in human, but it's a reference point to remember. I think Marsolais said this was in rats.

In addition, based on recently completed IND-enabling toxicity studies, Theratechnologies confirmed that TH1902 could be administered at three times the maximum tolerated dose (MTD) of docetaxel alone.

https://www.globenewswire.com/news-release/2020/12/08/2141188/0/en/Theratechnologies-Announces-New-Findings-for-its-Lead-Investigational-Compound-TH1902-for-the-Treatment-of-Several-Additional-Cancers.html


SPCEO1 wrote: The pre-clinical work suggests that therapeutic window might be unusually broad. How much confidence does this give you that the window might be similarly wide open in humans? Is there a chance the highest dose given in this trial does not show any nasty side-effects? It seems to me from the pre-clinical work, they have a good chance of being able to deliver a large dose of chemo safely and tolerably. Did they ever even get any serious neutropinia in the mice (perhaps as they have not shared all the data wth us)? If I recall correctly, they just stopped giving the mice doses at some point as there was no reason to continue, but I don't recall hearing that the doses described were ever too much for the mice to handle.

I also am assuming they have already safely, and without nasty toxicity, reached a dose level where the drug has a decent chance of having a positive impact on a tumor. Are you willing to assume that at this point? I think that is what you are implying by saying it is all now about finding the most therapeutic dose but wanted to check. Does assuming that gain some credibility by the fact they are expanding the trial at this point to two more centers?

My greatest concern going into the phase I was that it would be a quick flop because the human body would reject the PDC. Clearly, there are many concerns left to be dealth with but my confidence level in those hurdles being overcome is higher as the pre-clinical work seemed very strong and because TH seemed pretty confident about the trial last Monday. I would not be surprised if they have already seen some very preliminary indications that the drug is working as expected. But this is obviously all guesswork and we only have tiny hints to go off of at this point. I have said previously that since they are trailblazers in PDC cancer testing, TH therefore may not know what is around the next clincial corner as they move forward. Nevertheless, I am choosing to be encouraged by what I have heard so far. They really did not give us anything to get out of sorts about last Monday. My stroing impression was that TH is very pleased with the early stage of the phase I.  Hopefully, there is nothing too serious lurking around those blind corners!


qwerty22 wrote:

In non-cancer drug trial Ph1a is usually something like 6 healthy volunteers getting dose escalation to check for major reactions. I guess we are through the equivalent of that. It depends what you mean by safe though. If you mean patients haven't dropped dead or had a serious immediate reaction to the drug then probably yes we are over that hurdle. But it seems ever cancer drug has toxicity, after all the goal here is to kill cells directly or indirectly with the drug, the trick being to kill tumour cells and not healthy cells. So expect some toxicity, I read the way MTD is defined leads to a drug profile with 40-70% of patients having serious events, this is the price you pay for injecting cell killing drugs into a person. As an example, at the working dose of docetaxel around 30-40% get febrile neutropenia, infection and fever caused by a damaged immune system. So you can't really take about completely safe cancer drugs, expect some toxicity, the question is how much, when, is it manageable by the doctor and bearable by the patient.


Having got over that first hurdle then the real goal in this trial is to start to define the therapeutic window, the relationship between efficacy and toxicity. This is the meat of Part1 and we are right in the middle of that period and it will go on until they reach their top dose. The viability of the drug going forward really depends on that.

 

SPCEO1 wrote: As simply put as I can do it, we are at a place now where we can reasonably assume that TH-1902 is safe to use in humans and, if it shown to be efficacious, it is going to be a pretty big deal. Those who visit this website are among the relatively small number of investors who have any knowledge at all of this drug or its potential. With TH's management now confident enough in TH-1902 to give the presentation they gave a week ago, and with LSA's involvement, it stands to reason that the number of people gaining an understanding of this potential will be growing. So, while we will not have proof of concept efficacy data until most likely September/October, there should be a growing number of investors willing to take a chance on TH between now and then. If it is shown to be efficacious as well as safe, then our little group here on Stcokhouse will quickly be overwhelmed with new investors/speculators and the stock will take on an entirely new character. While the overall market trend is always a dominant factor in a share price's evolution, we should be seeing increasing buying interest in the weeks approaching the expected announcement of the efficacy data. 

If that data is really good, then it is off to the races for the stock obviously. If the data is just good, and not really good, then it will take longer (waiting for more data) for the stock to become a hot commodity. If the efficacy data is bad, then those who were betting on really good data will be sellers and the stock will give up some ground. The amount of ground given up will depend on how far the speculation about the efficacy data had driven the stock higher before it was announced. But we should expect that the number of people who are aware of the potential with TH-1902 will be growing in the weeks ahead.   

 

 





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