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Arch Biopartners Inc V.ARCH

Alternate Symbol(s):  ACHFF

Arch Biopartners Inc. is a late-stage clinical trial company focused on preventing acute kidney injury. The Company is developing a platform of new drugs to prevent inflammation injury in the kidneys, lungs and liver via the dipeptidase-1 (DPEP1) pathway and are relevant for many common injuries and diseases where organ inflammation is an unmet problem. The Company’s lead drug candidate is LSALT Peptide. The Company is engaged in the clinical development of LSALT Peptide and other DPEP-1 targeting drug candidates for indications where inflammation of the lungs, liver and kidneys is an unmet problem. LSALT Peptide is in a second phase II trial, targeting the prevention and treatment of cardiac surgery-associated acute kidney injury (CS-AKI). The Company has additional technology platforms in its portfolio, which are AB569 and Borg. AB569 is an anti-infective candidate for treating or preventing antibiotic resistant bacterial infections, primarily as a topical treatment for wounds.


TSXV:ARCH - Post by User

Post by Riverfolkon Jan 05, 2021 9:09am
99 Views
Post# 32222528

COVID19 NEWS-University of Calgary Joins the Phase II Trial

COVID19 NEWS-University of Calgary Joins the Phase II TrialUniversity of Calgary Joins the Phase II Trial of LSALT Peptide for the Treatment of Complications in Hospitalized COVID-19 Patients

2021-01-05 07:50:00 AM ET (GlobeNewswire)


 Arch Biopartners Inc. ("Arch" or the "Company") (TSX Venture: ARCH and OTCQB: ACHFF), announced today that the University of Calgary Cumming School of Medicine has joined the Phase II trial of its lead drug LSALT peptide (Metablok), targeting the prevention of acute lung injury, acute kidney injury, and other complications caused by inflammation in hospitalized patients with moderate to severe cases of COVID-19.


"We are particularly excited in launching this study in Calgary given that this treatment has its roots in basic science work performed here at the University. This novel treatment adds to our local investigational therapeutic options for patients admitted to hospital with COVID-19 disease and has great potential to reduce complications from this and other severe diseases that frequently result in lung and kidney injury," said Alain Tremblay MDCM, Professor at the Cumming School of Medicine, Respirologist and site principal investigator for the LSALT Phase II trial.


The addition of the Canadian site increases the number of countries participating in the Phase II trial to three, joining sites in the United States and in Turkey. Arch is currently exploring opportunities to add additional clinical sites in all three countries where the number of hospitalized COVID-19 patients has grown significantly.


Hospitalizations of COVID-19 patients have been on the increase as infection rates have surged throughout the world. In the last two weeks of December, Canada has had over 90,000 new infections and over 14,000 of these have been in Alberta.


About the Phase II trial for LSALT Peptide


The Phase II trial is an international, multicenter, randomized, double-blind, placebo-controlled, proof of concept study of LSALT peptide (Metablok) as prevention of organ inflammation known to trigger acute respiratory distress syndrome (ARDS) and acute kidney injury (AKI) in patients infected with SARS-CoV-2 (COVID-19). ARDS is the leading cause of death in COVID-infected patients. AKI has been observed in approximately 35% of patients admitted to hospital with COVID-19 and is also a leading cause of mortality.


The composite primary endpoint of the Phase II trial reflects the severe effects often experienced by hospitalized COVID-19 patients and deemed appropriate for LSALT peptide's novel mechanism of action in blocking consequential inflammation in the lungs, kidneys, and other organs.


Additional information about the Phase II trial can be found at:


https://clinicaltrials.gov/ct2/show/NCT04402957


The Phase II results will be used to design the Phase III program, including greater patient numbers to more fully evaluate efficacy and safety in COVID-19 patients.


About COVID-19


COVID-19 is the disease caused by the novel coronavirus SARS-CoV-2 that emerged in China in late 2019. Severe complications from COVID-19 are in large part due to excessive host immune responses to the virus that result in progressive lung inflammation and acute respiratory distress syndrome that often requires mechanical ventilation and critical care. Patients with severe COVID-19 also experience multiple organ dysfunction including acute kidney injury, liver dysfunction, cardiac failure, and blood abnormalities. Currently, no effective antiviral drug or specific treatment exists for SARS-CoV-2 infection. Treatment of severe COVID-19 has been primarily supportive, relying heavily on respiratory, infectious diseases, and critical care medicine.


Survival rates and health care system capacity could both be improved with new treatments that prevent the severe manifestations of COVID-19, such as worsening lung inflammation (ARDS) and AKI experienced by patients infected with SARS-CoV-2.


Hirsch JS et al. Acute kidney injury in patients hospitalized with COVID-19. Kidney Int. 2020


doi: https://doi.org/10.1016/j.kint.2020.05.006.


J. S. Ayres, Sci. Adv 10.1126/sciadv.abc1518 (2020)


About Arch Biopartners


Arch Biopartners Inc. is a clinical stage company focused on the development of innovative technologies that have the potential to make a significant medical or commercial impact.  Arch is developing a pipeline of new drug candidates that inhibit inflammation in the lungs, liver and kidneys via the dipeptidase-1 (DPEP-1) pathway for multiple medical indications.


For more information on Arch Biopartners, its technologies and other public documents Arch has filed on SEDAR, please visit www.archbiopartners.com


The Company has 61,212,302 common shares outstanding.
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