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

ProMIS Neurosciences Inc PMN

ProMIS Neurosciences Inc. is a clinical-stage biotechnology company. It is focused on generating and developing antibody therapeutics selectively targeting toxic misfolded proteins in neurodegenerative diseases such as Alzheimer’s disease (AD), amyotrophic lateral sclerosis (ALS) and multiple system atrophy (MSA). Its proprietary target discovery engine applies a thermodynamic, computational discovery platform-ProMIS and Collective Coordinates-to predict novel targets known as Disease Specific Epitopes on the molecular surface of misfolded proteins. Using this approach, the Company is developing novel antibody therapeutics for AD, ALS and MSA. Its product candidates are PMN310, PMN267, and PMN442. The PMN310 is a monoclonal antibody designed to treat AD by selectively targeting toxic, misfolded oligomers of amyloid-beta. PMN267 product candidate targeting ALS. PMN442 is a drug candidate being developed for MSA designed to selectively target and protect against pathogenic a-syn species.


NDAQ:PMN - Post by User

Post by Gbathaton Jun 04, 2021 6:35pm
195 Views
Post# 33334821

the big picture

the big pictureAducanumab is not great, but it would be a step in the right direction.  The question likely weighing on the FDA is the cost-benefit.  Hopefully they are considering the opportunity costs associated with next-gen product development and the impacts of their decision on the industry as a whole.

In a previous post, several options were presented- approval, rejection, or restricted approval.  I worry the latter might also restrict the potential benefits associated with early intervention based on biomarkers. 

As an APOE-4 variant carrier (just found that out last week thanks to 23andme), I'd be okay with approval. Thankfully, I've got a couple decades between now and possible onset.  

As a PMN shareholder, I'd definitely be okay with approval!  

Enjoy your weekend.  Monday could be interesting... 8-)


<< Previous
Bullboard Posts
Next >>