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Bullboard - Stock Discussion Forum 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... see more

TSX:TH - Post Discussion

Theratechnologies Inc > No value for Pipeline
View:
Post by SPCEO1 on Jan 16, 2021 9:19am

No value for Pipeline

With the cash adjusted market cap at less than 3x revenues, it is pretty clear the market is giving no value to either NASH or cancer. Cancer is understandable since we have no human test results yet. On NASH, if you exclude Europe, then my suggestion that TH's discount to MDGL and NGM' valuation of 40% should probably rise to 70% since half the NASH market could be unavailable to TH. Even assuming that, THTX should still probably sell at around $7-$8 on a conservative basis ($2 for the legacy drugs and $5.50 for the US NASH business). You could also bump that 70% discount lower to 60 or 65% to reflect the better profitability of the US NASH market versus Europe.
Comment by scarlet1967 on Jan 16, 2021 10:29am
I don't think you would ascribe zero value to a phase 1 trial for a cancer drug, even the preclinical stage has a value, the company paid for the PDC preclinical and there are many companies at even preclinical stage which have been ascribed some sort of valuation based on their progress in the preclinical stage, the market for the indication and cost of the trials so there is NPV for all ...more  
Comment by scarlet1967 on Jan 16, 2021 10:30am
https://www.baybridgebio.com/drug_valuation.html
Comment by qwerty22 on Jan 16, 2021 12:53pm
If we go with the worst case scenario and they don't do the trial with the EMA, I don't know that data generated for the FDA can't be used for an EMA approval. All we are talking about is the present moment in time. The EMA doesn't like the present data set, they may like the future dataset once they have the Ph3 data. Here's my take on a possible scenario. The EMA muddies ...more  
Comment by SPCEO1 on Jan 16, 2021 1:21pm
That was an excellent take on the situation. I do think there is a 90% chance the FDA's approval of TH moving forward on a phase III is a done deal. So, RBC's take seems like a lame attempt by him to talk that down. TH announced it so he really should have done respect for that. Unless he views them as untrustworthy, which based on what we have seen recently might have more validity than ...more  
Comment by longterm56 on Jan 16, 2021 1:23pm
Comment by Bucknelly21 on Jan 16, 2021 1:48pm
We are always a couple months out ... so true 
Comment by scarlet1967 on Jan 16, 2021 2:15pm
They said they got the letter to go a head with NASH phase 3 but need to adjust the protocol so I am not sure why we still put probability rate on it. Even if the EMA's approval is questionable that alone shouldn't rush them to close a low ball deal as the whole NASH was questionable just before the good PR. The good PR stated record sales when nobody would bet on it, many questioned ...more  
Comment by palinc2000 on Jan 16, 2021 2:23pm
The momentum was Halted !!!! WHY?
Comment by scarlet1967 on Jan 16, 2021 2:35pm
Ultra conservative somehow insecure old fashioned board members surrounding , influencing our CEO.
Comment by qwerty22 on Jan 16, 2021 3:47pm
But unfortunately it seems true. "The end of the regulatory process" has been the goal for 2 years and we are still not quite there. If you're wondering about their ability to market stuff, they've been selling that story to us for 2 years and we've been buying it. I'm still buying it now even after the recent kick in the unmentionables.
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