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Algernon Pharmaceuticals Inc. C.AGN

Alternate Symbol(s):  AGNPF

Algernon Pharmaceuticals Inc. is a clinical-stage drug development company. The Company is focused on developing repurposed therapeutic drugs in the areas of non-alcoholic steatohepatitis (NASH), a type of liver disease, chronic kidney disease (CKD), inflammatory bowel disease (IBD), idiopathic pulmonary fibrosis (IPF) and chronic cough as well as advancing a stroke program using N, N-Dimethyltryptamine (DMT). The Company operates through two segments, which includes the development of repurposed therapeutic drugs in Canada and the facilitation of the Company’s lead drug candidates into off-label phase II clinical trials (humans) in Australia. The Company's pipeline includes NP-251 (Repirinast) and AP-188 (DMT). The Company, through its subsidiary, Algernon NeuroScience Inc., is developing AP-188 (DMT) as a potential treatment for stroke and traumatic brain injury (TBI) recovery. Its NP-251 is being developed as a potential treatment for kidney inflammation and fibrosis.


CSE:AGN - Post by User

Post by NamesJebon Oct 16, 2020 2:33pm
136 Views
Post# 31729582

https://link.springer.com/article/10.1007/s12035-020-02070-6

https://link.springer.com/article/10.1007/s12035-020-02070-6
Specific Considerations for Neuroinvasion in COVID-19 With the probable SARS-CoV2 neuroinvasion, it is worth considering the specific treatment options in addition to the current COVID-19 management protocol. Apart from the antiviral strategy, there were animal studies on the possibility of modulating CNS excitatory pathways, i.e., the glutamate homeostasis [58,59,60]. A known N-methyl-D-aspartate (NDMA) receptor antagonist, memantine, improved the symptoms, reduced motor disabilities, and the viral replication in coronavirus-infected mice [58]. Other NMDA receptor blockers, including dizocilpine, agmatine sulfate, and ifenprodil, also reduced the neuronal death, the intraocular pressure (IOP), the reactive gliosis, and the neurodegeneration in the ZIKA-infected mice [59]. A glutamine antagonist, 6-diazo-5-oxo-l-norleucine, reduced CNS leukocyte migration, prevented inflammation, paralysis, and death in mice [60]. With the worsening prognosis of SARS-CoV2 neuroinvasion, these options are probably reserved for compassionate considerations.
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