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Revive Therapeutics Ltd C.RVV

Alternate Symbol(s):  RVVTF

Revive Therapeutics Ltd. is a Canada-based life sciences company. The Company is focused on the research and development of therapeutics and diagnostics for infectious diseases, medical countermeasures, and rare disorders. It is engaged in exploring the use of Bucillamine for the potential treatment of nerve agent exposure and long COVID. The Company, through its diagnostics division, is evaluating a point-of-care in vitro diagnostic device that aids in the detection of post COVID-19 conditions or Long COVID. It also advancing the development of Psilocybin-based therapeutics through various programs. The Company's subsidiaries include Revive Therapeutics Inc. (Ontario), Revive Diagnostics Inc., and Psilocin Pharma Corp. (Ontario).


CSE:RVV - Post by User

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Post by mrnormalon Oct 04, 2020 7:49pm
737 Views
Post# 31665001

IV NAC Therapy and why Bucillamine Will Work

IV NAC Therapy and why Bucillamine Will Work

https://www.sciencedirect.com/science/article/pii/S1521661620306513?fbclid=IwAR2R7cS_qxdtdV0A-FUcvMONoUj_y9l_fyAS9rgN4q0Rt8Q9DxEJfjDqDbQ

We describe a remarkable benefit of IV NAC in severe COVID-19 infection. As expected, IV NAC initially mitigated the hemolysis in a G6PD-deficient, COVID-19-infected patient treated with hydroxychloroquine for a single day. We also observed an obvious drop in inflammatory markers following initial NAC administration. This was followed by rebound rises of CRP and ferritin upon discontinuation of NAC. Re-started IV NAC for two additional intervals resulted in repeated drops in CRP and ferritin levels (Fig. 1B). NAC administration allowed the discontinuation of ECMO and eventual discharge of the patient to his home.

NAC mechanism of action may involve the blockade of viral infection and the ensuing cytokine storm that warrant follow-up confirmatory studies in the setting of controlled clinical trials.

https://www.biospace.com/article/releases/revive-therapeutics-announces-u-s-fda-approval-of-confirmatory-phase-3-clinical-trial-for-bucillamine-in-covid-19/

Scientific Rationale of Bucillamine for COVID-19

Preclinical and clinical studies have demonstrated that reactive oxygen species contribute to the destruction and programmed cell death of pulmonary epithelial cells.1 N-acetyl-cysteine (NAC) has been shown to significantly attenuate clinical symptoms in respiratory viral infections in animals and humans, primarily via donation of thiols to increase antioxidant activity of cellular glutathione2,3,4,5. Bucillamine (N-(mercapto-2-methylpropionyl)-l-cysteine) has a well-known safety profile and is prescribed in the treatment of rheumatoid arthritis in Japan and South Korea for over 30 years. Bucillamine, a cysteine derivative with two thiol groups, has been shown to be 16 times more potent as a thiol donor in vivo than NAC 6. The drug is non-toxic with high cellular permeability. The basis of the clinical study will analyze if Bucillamine has the potential, via increasing glutathione activity and other anti-inflammatory activity, to lessen the destructive consequences of SARS-CoV2 infection in the lungs and attenuate the clinical course of COVID-19.
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