Northwire Canada EditionSunday, July 12, 2026
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Arch Biopartners announces Royal Columbian Hospital has dosed its first patient in its Phase II cardiac surgery-associated AKI trial

Arch Biopartners Doses First Patient in Phase II AKI Trial Amidst Dilution Concerns

Executive Summary
  • Royal Columbian Hospital (RCH) has dosed its first patient in Arch Biopartners' ongoing Phase II clinical trial for LSALT peptide.
  • The trial targets cardiac surgery-associated acute kidney injury (CS-AKI).
  • RCH is the fourth active dosing site in Canada, with recruitment continuing at Toronto General, St. Michael’s Hospital, and University of Calgary.
  • Company is in feasibility discussions for four prospective sites in the United States and one additional site in Ontario.
  • Recruitment target remains 240 patients across a multi-center, randomized, double-blind, placebo-controlled study.
  • CEO Richard Muruve confirms steady progress toward establishing LSALT peptide as a new drug to reduce AKI incidence and dialysis needs.
Material Impact
  • The news represents expected clinical progression following the April 30 announcement that RCH began patient recruitment.
  • Dosing of the first patient is a standard operational milestone rather than a data readout or efficacy confirmation, limiting immediate upside potential.
  • No new safety concerns (SUSARs) were reported in previous updates, maintaining the status quo on risk profile.
  • The announcement does not alter the capital structure or financing needs immediately but confirms burn rate continues as expected for Phase II execution.
  • Given the stock price ($0.44) is significantly below the recent private placement price ($0.60 in April 2026), positive news has limited ability to reverse sentiment without data readouts.
ARCH · Price
Company Overview
  • Company: Arch Biopartners Inc., focused on therapies for acute kidney injury (AKI) and chronic kidney disease (CKD).
  • Flagship Project: LSALT peptide in Phase II trial for cardiac surgery-associated AKI (CS-AKI).
  • Secondary Asset: Cilastatin in Phase II trial for toxin-induced AKI.
  • Pipeline Expansion: CKD platform targeting IL-32 cytokine, acquired via Lipdro Therapeutics acquisition in November 2025.
  • Scientific Basis: LSALT targets DPEP1-mediated inflammation; preclinical data published in Cell (2019) and Science Advances (2022).
Read the original news release →

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