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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

Comment by C10H12N2on Dec 19, 2021 3:10pm
87 Views
Post# 34245045

RE:Q&A: CEO's Statement(s) Regarding Chronic Cough Competition

RE:Q&A: CEO's Statement(s) Regarding Chronic Cough Competition Correction - 

In my opinion:


As of right now, Bellus Health appears to have the best clinical trial results to beat with a reported 34% reduction in Cough. However, Bellus Health’s drug is limited to severe cases of Chronic Cough. Bellus Health defines a severe cough as 25 coughs or more per hour.


The European Respiratory Journal (ERJ) states those with a respiratory disease will cough as frequent as 11 coughs per hour and women in particular will cough as frequent as 16 coughs per hour. Thus, the broader market for Chronic Cough remains wide open even if Bellus Health is successful at Phase lll of the clinical trial process.


As it relates to Merck’s drug the taste tolerability remains a huge issue. It’s an issue that remains in the hands of the FDA for a market approval delayed until next March 2022:


The FDA is delaying its decision on Merck’s gefapixant by at least a few months to “provide time for a full review of the submission,” the company revealed in an SEC filing. The agency, which originally set a PDUFA date for Dec. 21, now expects to make a decision by March 21

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