Arch Biopartners Inc., (“Arch” or the “Company”) (TSX Venture: ARCH
and OTCQB: ACHFF), announced today that three additional clinical
sites in Turkey have 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.
The three new hospitals joining the Phase II
study are Istanbul University-Cerrahpaşa, Sütçü İmam University
Hospital in the city of Kahramanmaraş, and the Gazi University
Hospital in Ankara, the capital of Turkey. The trial now has a
total of seven clinical sites across Turkey and Canada.
About the Phase II trial for LSALT
Peptide targeting CS-AKI
Arch Biopartners is currently sponsoring a Phase
II trial for LSALT peptide targeting cardiac surgery-associated
acute kidney injury (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. At present,
there are no therapeutic treatments available to prevent or treat
CS-AKI or IRI.
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.
LSALT peptide has been shown by Arch scientists
and their collaborators to prevent ischemia-reperfusion injury to
the kidneys in pre-clinical models (Video Link to pre-clinical
proof of concept). Details of their findings were published in a
Science Advances publication, titled “Dipeptidase-1 governs renal
inflammation during ischemia reperfusion injury” by Lau et.
al. and can be found at the Science Advances website.
Details of the Phase II trial, entitled “Phase 2
Global, Multicenter, Randomized, Double-Blind, Placebo-Controlled
Study of LSALT peptide for the Prevention or Attenuation of Acute
Kidney Injury (AKI) in Patients Undergoing On-Pump Cardiac Surgery”
can be viewed at clinicaltrials.gov.
About LSALT Peptide
LSALT peptide is a novel peptide drug candidate
and DPEP-1 inhibitor. In August 2019, a scientific team led by Arch
scientists Dr. Donna Senger and Dr. Stephen Robbins published a
paper in the journal Cell describing a novel mechanism of action
for organ inflammation in pre-clinical studies. In the publication,
DPEP-1 was identified, for the first time, as a major leukocyte
(white blood cell) adhesion receptor on the lung, liver and
kidney endothelium. DPEP-1 was also identified as the target
of LSALT peptide, differing from typical anti-inflammatory drugs by
targeting this novel adhesion receptor rather than targeting
individual cytokines, of which there are many.
See the 2019 Cell publication, titled
“Dipeptidase-1 is an adhesion receptor for neutrophil recruitment
in lungs and liver” by Choudhry et. Al. available at the Cell
website.
Arch Biopartners’ clinical team published a peer
reviewed publication in the British Medical Journal Open (BMJ Open
– March 2024, Vol 14, Issue 3) detailing the clinical and biomarker
results of the international Phase II human trial for LSALT peptide
targeting acute lung and kidney inflammation in hospitalized
patients infected with SARS-CoV-2 virus. See the full publication
at the BMJ Open website.
About Arch Biopartners
Arch Biopartners Inc. is a late-stage clinical
trial company focused on preventing inflammation and acute organ
injury. The Company is developing new drug candidates that inhibit
inflammation in the lungs, kidneys, and liver via the dipeptidase-1
(DPEP-1) pathway and are relevant for common injuries and diseases
where organ inflammation is an unmet problem.
For more information on Arch Biopartners'
science and technologies, please visit:
www.archbiopartners.com/our-science
For investor information and other public
documents the company has filed on SEDAR+, please visit
www.archbiopartners.com/investor-hub
The Company has 62,755,633 common shares outstanding.
Forward-Looking Statements
This press release contains forward-looking
statements within the meaning of applicable Canadian securities
laws regarding expectations of our future performance, liquidity
and capital resources, as well as the ongoing clinical development
of our drug candidates targeting the dipeptidase-1 (DPEP-1)
pathway, including the outcome of our clinical trials relating to
LSALT peptide (Metablok), the successful commercialization and
marketing of our drug candidates, whether we will receive, and the
timing and costs of obtaining, regulatory approvals in Canada, the
United States, Europe and other countries, our ability to raise
capital to fund our business plans, the efficacy of our drug
candidates compared to the drug candidates developed by our
competitors, our ability to retain and attract key management
personnel, and the breadth of, and our ability to protect, our
intellectual property portfolio. These statements are based on
management’s current expectations and beliefs, including certain
factors and assumptions, as described in our most recent annual
audited financial statements and related management discussion and
analysis under the heading “Business Risks and Uncertainties”. As a
result of these risks and uncertainties, or other unknown risks and
uncertainties, our actual results may differ materially from those
contained in any forward-looking statements. The words “believe”,
“may”, “plan”, “will”, “estimate”, “continue”, “anticipate”,
“intend”, “expect” and similar expressions are intended to identify
forward-looking statements, although not all forward-looking
statements contain these identifying words. We undertake no
obligation to update forward-looking statements, except as required
by law. Additional information relating to Arch Biopartners Inc.,
including our most recent annual audited financial statements, is
available by accessing the Canadian Securities Administrators’
System for Electronic Document Analysis and Retrieval (“SEDAR”)
website at www.sedarplus.ca.
The science and medical contents of this release
have been approved by the Company’s Chief Science Officer
Neither TSX Venture Exchange nor its Regulation
Services Provider (as that term is defined in the policies of the
TSX Venture Exchange) accepts responsibility for the adequacy or
accuracy of this release
For more information, please contact:
Richard Muruve
Chief Executive Officer
Arch Biopartners, Inc.
647-428-7031
info@archbiopartners.com
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