CatalystWireBeta

Update on Launch of CIZ1B Biomarker Assay

In brief · summary, not quotable

iGenomeDX appointed as first COLA and CLIA accredited laboratory to launch CIZ1B biomarker test commercially in USA.

  • Guaranteed payments from BIO licensing deal (through April 2027) US$2.4 million
  • Payments received to date from BIO US$400,000
  • Caribbean territory early payments (July 2025) US$250,000
  • Caribbean territory early payments (September 2025) US$250,000
Full announcement

Select text to share a quote on X · sign in to keep highlights & notes in your CIZ notes

Cizzle Biotechnology, the UK based diagnostics developer of early cancer tests, is pleased to announce that its licensing partner Cizzle Bio Inc ("BIO" or "Cizzle Bio") has appointed iGenomeDX, a specialist clinical diagnostics laboratory to launch the Company's first commercial CIZ1B biomarker test in the USA. iGenomeDX is a Commission on Office Laboratory Accreditation ("COLA") accredited and Clinical Laboratory Improvement Amendments ("CLIA") certified clinical laboratory and has been establishing operating and quality systems ahead of offering the test to clinicians for the first time.

Key Highlights

  • iGenoneDX appointed by BIO as first clinical diagnostics laboratory to offer commercial CIZ1B biomarker testing.
  • This follows successful collaboration and support between Cizzle, iGenomeDX and BIO to complete an operational and quality systems programme designed to meet the exacting standards required in iGenomeDX's COLA accredited, CLIA certified laboratory, designated to validate CIZ1b as a laboratory developed test for commercial use ahead of the launch of the CIZ1B biomarker test.

Background

On 21 October 2024 the Company announced an exclusive licensing and partnership agreement with BIO for its proprietary CIZ1B biomarker test to help detect early-stage lung cancer, throughout the USA and Canada. The Company has since received payments of US$400,000 due from initial exclusivity fees and advanced royalties as part of guaranteed payments totalling US$2.4 million over the period ending April 2027. The Company has now extended that agreement, as announced on 16 December 2024, to cover the 14 Sovereign States of the Caribbean and the Cayman Islands ("Caribbean") triggering early payments totalling US$250,000 in July 2025 and US$250,000 in September 2025.

The appointment of iGenomeDX by BIO, a specialist clinical diagnostics laboratory, is the next step in the Company's plan to achieve commercial sales later this year by providing an accredited facility to launch the CIZ1B biomarker test. The accreditation process involved an evaluation of a laboratory's operations, including its testing procedures, quality control, personnel qualifications, and compliance with regulatory requirements. Labs that achieve COLA accreditation demonstrate a commitment to maintaining high standards of accuracy, reliability, and patient safety in diagnostic testing to ensure they meet CLIA standards and can legally operate.

The successful completion of the operational and quality systems programme is necessary for launching a cost-effective and scalable version of the CIZ1B biomarker assay with rigorous quality control requirements to meet expected reproducibility and sensitivity. This will demonstrate the test is commercially scalable and can be rolled out as a global solution to help reduce premature cancer deaths and improve survival rates and quality of life for cancer patients.

Commenting, Allan Syms, Executive Chairman of Cizzle Biotechnology, said:

"I am delighted to announce the positive progress being made by our partners Cizzle Bio who have appointed the first of their COLA and CLIA accredited clinical diagnostics laboratories to bring our CIZ1B Biomarker test for early-stage lung cancer to market. In the short time since we began our exclusive licensing partnership with Cizzle Bio, they have initiated multiple ongoing partnerships with several National Cancer Institute (NCI) designated cancer centres throughout the United States, with the goal of enhancing early detection capabilities for lung cancer. They have strengthened their leadership team with industry and clinical expertise and in creating the launchpad for our CIZ1B biomarker test. In collaboration with Cizzle Bio we continue to work closely with iGenomeDX's exceptional leadership and technical team to ensure a seamless transition of technology into the clinic. We look forward to sharing updates on their first commercially available tests in the near future."

You can also follow the Company through its twitter account @CizzlePlc and on LinkedIn.

iGenomeDx is a COLA accredited and CLIA certified clinical diagnostics company based in San Antonio, Texas meeting U.S. federal standards that ensures quality and reliability in laboratory testing for human specimens. Their mission is to enhance physician decision-making, improve patient care, and reduce healthcare costs by providing reliable genetic testing services. iGenomeDx offers pharmacogenomic tests to help physicians personalize medication choices and dosages based on an individual's genetic makeup, as well as molecular diagnostics for infectious diseases such as respiratory, urinary tract, wound, and nail infections. They also provide therapeutic drug monitoring to assess medication adherence.

Cleaned text: letterheads, contacts and legal notices removed. View the original announcement ↗ · Company filings. Not investment advice.

Share this quote

Quote card
Post on X WhatsApp Download image

The link opens this announcement with the quote highlighted. Quotes are checked against the original text.

Add a note