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  3. Arch Biopartners Univ Of Calgary Join Hands For Lsalt Peptide Trial
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  • 19 Mar 2024
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Arch Biopartners & Univ of Calgary Join Hands for LSALT Peptide Trial

Arch Biopartners announces Univ of Calgary joins with phase II trial of LSALT peptide to treat cardiac surgery-associated acute kidney injury

Overview

Arch Biopartners Inc, a late-stage clinical trial company focused on preventing inflammation and acute organ injury, has announced that a research team from the University of Calgary’s Cumming School of Medicine has joined the phase II trial for LSALT peptide targeting the prevention and treatment of cardiac surgery-associated acute kidney injury (CS-AKI). LSALT peptide is the Company’s lead drug candidate for preventing and treating inflammation injury in the kidneys, lungs and liver.

Words from Principal Investigator

“We know that acute kidney injury impairs recovery and can negatively affect long-term outcomes following heart surgery. Our research team is excited to participate in a study working towards improving kidney health in our patients.” said Alex Gregory MD, Assistant Professor and Director of Research, Division of Cardiovascular Anesthesia at the Libin Cardiovascular Institute at the Cumming School of Medicine, and site principal investigator for the LSALT Phase II CS-AKI trial.

Dr. Gregory’s clinical team has submitted an application to the local Research Ethics Board for permission to participate in the trial.

Clinical Sites

  • The addition of the first Canadian clinical site increases the number of trial sites to four, with three hospitals in Turkey currently recruiting patients. 
  • There are three additional hospital sites in Turkey pending activation into the trial. 
  • The Arch Biopartners team is currently working with two other hospital sites in Canada to prepare for their participation in this phase II trial.

CS-AKI Phase II Trial

  • The CS-AKI phase II trial is an international multi-center, randomized, double-blind, placebo-controlled study of LSALT peptide. 
  • The recruitment target for the trial is 240 patients. The primary objective of the trial is to evaluate the percentage of subjects with AKI within seven days following on-pump (heart-lung machine) cardiac surgery, defined by the KDIGO (Kidney Disease: Improving Global Outcomes) criteria.

About CS-AKI

  • CS-AKI is often caused by ischemia-reperfusion injury (IRI) that reduces blood flow (ischemia) and thus oxygen in the kidney, causing kidney cell damage. 
  • Once blood flow is restored to normal (reperfusion), inflammation is triggered and injury to kidney cells is exacerbated. 
  • In the worst cases of AKI, kidneys fail, leading to kidney dialysis or kidney transplant. There is no treatment available in the market today that prevents acute kidney injury of the type commonly experienced by on-pump cardiac surgery patients.

Acute Kidney Injury

Acute kidney injury is a known common complication in patients after coronary artery bypass grafting (CABG) and other cardiac surgeries, including on-pump surgeries which increase the risk of acute kidney injury. The reported prevalence of CS-AKI is up to 30% and is independently associated with an increase in morbidity and mortality.

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