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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 NamesJebon Sep 17, 2020 2:22pm
136 Views
Post# 31577512

RE:150 enrolled ???

RE:150 enrolled ???
talisman47 wrote: Interesting that half way thru this article it says 150 patients have been enrolled ! Don't know if true or just a wrong statement by whoever wrote the article ???


https://www.clinicaltrialsarena.com/news/algernon-ifenprodil-covid-trial/


Probably supposed to read more along the lines of this : "With positive preliminary data from the Phase 2b study of a total of 150 patients, the clinical trial will move directly into Phase 3. The data from the Phase 2b study will determine the number of patients needed to reach statistical significance in the Phase 3 trial. Patients are randomized in a one-to-one manner and will either be treated using an existing standard of care, or standard of care plus Ifenprodil 60 mg (taken as one 20mg tablet three times a day) for one arm or standard of care plus Ifenprodil 120 mg (taken as two 20 mg tablets three times daily) for two weeks. Algernon said it would update on a projected completion date of the study, as well as when the read-out of the data can be expected when enrollment in the study reaches 50%."
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