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RNS Number : 8300W Cizzle Biotechnology Holdings PLC 18 July 2024
18 July 2024
Cizzle Biotechnology Holdings plc
("Cizzle", "Cizzle Biotechnology", or "the Company")
Manufacturing Agreement with BBI Solutions
Cizzle Biotechnology, the UK-based diagnostics company focused on developing a
cost effective biomarker test to help detect early-stage lung cancer, is
pleased to announce a strategic agreement with BBI Solutions ("BBI"), the
world's largest independent producer of immunodiagnostic reagents, to supply
its first order of commercial propriety monoclonal antibodies. This
collaboration is a significant milestone in Cizzle's mission to commercialise
its cost-effective biomarker test for early-stage lung cancer detection.
This initial order of CIZ1B commercial propriety monoclonal antibodies from
BBI is crucial for advancing the clinical evaluation process, marking a vital
step towards bringing the test to market. These antibodies will be
manufactured at BBI's ISO 13485-certified facilities and are expected to
support up to 5000 assays for detecting the CIZ1B biomarker, which is strongly
associated with early-stage lung cancer.
The antibodies produced will be used in a clinical evaluation of patients with
suspicious indeterminant (undiagnosed) lung nodules for lung cancer with a
major cancer centre in the USA. This evaluation is ahead of the planned
rollout of commercial tests by the Company's intended licensing partner in the
USA, Cizzle Bio Inc ("BIO"). Additionally, this partnership supports the
development of a point of care ("POC") assay and the Company's broader plans
to explore the utility of CIZ1B for detecting other cancers.
Key Highlights:
· Partnership with BBI Solutions: BBI will manufacture commercial
CIZ1B monoclonal antibodies.
· Certified Manufacturing: Production in ISO 13485-certified
facilities ensures adherence to stringent quality standards.
· Sufficient Initial Supply: The first batch will support up to
5000 blood tests for the CIZ1B biomarker.
· Supporting Clinical Evaluation: The antibodies will facilitate
clinical evaluations with a major US cancer centre, critical for confirming
the presence of lung cancer in patients with indeterminate lung nodules
identified by CT scans.
Commercialization and Regulatory Strategy
The antibodies being produced will support Cizzle's ongoing commercialisation
and regulatory strategy, including:
· US CLIA accreditation: As announced on 17 June 2024, BIO aims to
register its first US CLIA (Clinical Laboratory Improvement Amendments)
accredited lab with the FDA (US Food and Drug Administration) for the CIZ1B
LDT test in September 2024.
· CLIA certification and product launch: BIO plan to achieve CLIA
certification for the LDT in November 2024, with an anticipated product launch
and insurer reimbursement code achievement by April 2025.
· Point of Care ("POC") development: Plans include developing a POC
test for use in pharmacies, doctors' offices, and by healthcare providers.
· Expanded research: Continued R&D at the University of York to
explore the utility of CIZ1B in detecting other cancers.
It is essential that reagents, including the Company's monoclonal antibodies,
meet strict regulatory requirements. The ISO standards (International
Organization for Standardization) provide a platform to bring globally
accepted standards together and in the case of medical devices, which includes
in vitro diagnostics, ISO 13485 is the Quality Management System applicable to
the regulatory requirements for a business operating in the medical device
sector*. BBI will be producing the Company's antibodies within their ISO13485
certified facilities for custom manufacture of antibodies.
*PUB100422_preview.pdf (iso.org)
(https://www.iso.org/files/live/sites/isoorg/files/store/en/PUB100422_preview.pdf)
Further Information
With nearly 5000 lives lost daily to lung cancer, largely due to the lack of a
simple early detection test, Cizzle is dedicated to bringing its proprietary
CIZ1B test to market as quickly as possible. This partnership with BBI is a
pivotal step in providing reliable clinical results and developing a
user-friendly point-of-care test.
The supply of the new commercial monoclonal antibodies will be used to provide
clinical results on patients suspected to have early-stage lung cancer arising
from CT scanning in the US cancer centre, developing a simple finger prick
point of care test for the CIZ1B biomarker and continuing Cizzle's work to
determine the utility of the test for other cancers.
In addition, the Company's ongoing assay development and clinical evaluations
are supported by Cizzle's renewed research and development contract with the
University of York, announced on 17 June 2024. Subject to local ethical
approvals, the new phase of work will provide clinical results on patients
with suspected early-stage lung cancer arising from CT scanning at a leading
US cancer centre.
Allan Syms, Executive Chairman of Cizzle Biotechnology, said: "We are making
significant progress in bringing the company's CIZ1B test to market. CIZ1B is
highly associated with early-stage lung cancer and after extensive and
dedicated research at the University of York, we are now at a point where the
test will be made available to clinicians and patients to help in the drive to
detect cancer early and as a result save lives. A key step in making the test
commercial is to partner with a trusted global manufacturer with the skills,
experience and first-class quality-assured facilities to produce reliable,
robust and reproducible antibodies. Hence we are delighted to be partnering
with BBI solutions to make our first batch of antibodies for use in clinical
evaluations and trials, before rolling out the test across North America and
importantly investigating whether CIZ1B is relevant in detection other
cancers. I believe this is an inflection point in the Company's development
and now through working with BBI we have the capability to accelerate growth
by being able to produce our essential antibodies at scale."
Mario Gualano, CEO of BBI, added: "We are excited to partner with Cizzle
Biotechnology in their mission to bring an innovative lung cancer detection
test to market. Our expertise in producing high-quality immunodiagnostic
reagents will ensure that Cizzle's CIZ1B monoclonal antibodies meet the
highest standards. We are proud to contribute to a project that has the
potential to significantly improve early cancer detection and patient outcomes
globally."
Enquiries
Cizzle Biotechnology Holdings plc Via IFC Advisory
Allan Syms (Executive Chairman)
Allenby Capital Limited +44(0) 20 3328 5656
John Depasquale / George Payne (Corporate Finance)
Stefano Aquilino / Amrit Nahal (Sales and Corporate Broking)
Novum Securities Limited +44(0) 20 7399 9400
Colin Rowbury / Jon Bellis
IFC Advisory Limited +44(0) 20 3934 6630
Tim Metcalfe / Florence Chandler
About Cizzle Biotechnology
Cizzle is developing a blood test to help in the early detection of lung
cancer. The Company was spun out from the University of York, in 2006, around
the work of Professor Coverley and colleagues and was admitted to the Standard
segment of the main market of the London Stock Exchange in May 2021. Its test
is based on the ability to detect a stable plasma biomarker, a variant of CIZ1
known as CIZ1B. Normal CIZ1 is a naturally occurring cell nuclear protein
involved in DNA replication, and the targeted CIZ1B variant has been shown to
be highly correlated with early-stage lung cancer. For more information,
please see https://cizzlebiotechnology.com (https://cizzlebiotechnology.com/)
You can also follow the Company through its twitter account @CizzlePlc and on
LinkedIn.
About Cizzle Bio
Cizzle Bio Inc, a company registered in Texas USA, has been created by a group
of high-net-worth individuals with a passion to improve cancer patient
survival. Recognising that one of the main causes of poor survival rates for
certain cancers, and in particular lung cancer, is because diagnosis is often
when the disease is at an advanced state, there is an unmet need for a simple
blood test that can be used to detect cancer early.
BIO is led by Bill Behnke, who has been pioneering Cizzle Biotechnology's
marketing activities in the USA and is an accomplished entrepreneur and
performance-driven senior executive with an extensive background of success in
funding and building healthcare businesses through direct sales, marketing,
sales management, and business development. He is heavily engaged in
charitable work for cancer, and served a nine-year tenure on the national
board of the Leukemia and Lymphoma Society. He currently serves on the boards
of the ASCO Foundation's Conquer Cancer; the AYA Cancer Foundation; The
Wheeler Group; Children's Shelter of San Antonio; South Texas Blood and Tissue
Center; and the Leukemia and Lymphoma Society.
About BBI
BBI Solutions stands at the forefront of the global immunodiagnostic reagents
industry, leveraging over 5 decades of expertise in In Vitro Diagnostics
(IVD). The company specializes in high-quality raw materials and custom
development solutions, supporting lateral flow test development and
manufacturing. The company's ISO 13485 certification underscores its adherence
to the highest global standards, ensuring superior performance and compliance.
Annually, BBI's reagents play a pivotal role in 400 million lateral flow tests
and are a trusted component in 5 billion blood glucose test strips -showcasing
the company's significant contribution to global health and solidifying its
reputation as an industry leader.
With a focus on quality and customization, combined with a robust pipeline of
recombinant products, BBI Solutions continues to meet the evolving demands of
the market. Providing precise, cutting-edge solutions, guaranteeing its
partners' assays achieve market prominence and contribute to transformative
patient outcomes.
For more information visit BBI Solutions | Lateral Flow, Reagents and POCT
(https://www.bbisolutions.com/)
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