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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 azzymaaon May 13, 2022 2:22pm
244 Views
Post# 34682418

Leede Jones Gable starts ProMIS at speculative buy; PT 50

Leede Jones Gable starts ProMIS at speculative buy; PT 50https://biotuesdays.com/2022/05/11/leede-jones-gable-start-promis-at-speculative-buy-pt-50-cents-canadian/

Leede Jones Gable starts ProMIS at speculative buy; PT 50 cents (Canadian)

ProMIS Neurosciences

Leede Jones Gable initiated coverage of ProMIS Neurosciences (TSX:PMN) with a “speculative buy” rating and price target of 50 cents (Canadian). The stock closed at 11 cents on May 10. 

The firm’s lead preclinical asset is, PMN310, a humanized monoclonal antibody (mAb) drug that selectively targets epitopes within misfolded toxic amyloid-beta oligomers. These are an intermediate form of brain-derived amyloid protein that available biochemical evidence is showing to be tightly associated with pathophysiology of Alzheimer’s disease. 

“ProMIS’ core competency lies in its expertise in generating mAbs that target conformational epitopes that are expressed either predominantly or exclusively on misfolded or aggregated proteins that in being misfolded/aggregated contribute to disease,” writes analyst Doug Loe, Ph.D., adding that this expertise has been applied to a suite of mAb therapies and not just PMN310. 

Dr. Loe said Alzheimer’s disease is a hugely competitive medical market, but with few clinical-stage assets targeting toxic amyloid oligomers, as PMN310 is. 

“We believe that PMN310 rises above its peers in not only targeting this intermediate aggregation form of beta-amyloid, but also from being specifically designed to do so and thus to manifest fewer off-target side effects,” he said. 

“This is in contrast to other therapies, including other beta-amyloid-targeted mAbs that simultaneously bind to beta-amyloid monomers or fibrils that we believe are less relevant to Alzheimer’s disease progression,” he added. 


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