Subject: IMA
Immunovia: CPT PLA Code for the IMMraytm PanCan-d test approved
LUND, Sweden, July 5, 2022 /PRNewswire/ -- Immunovia AB (NASDAQ Stockholm: IMMNOV) announced, that Immunovia, Inc., its American subsidiary, has recently received approval for a Current Procedural Terminology (CPT) Proprietary Laboratory Analyses (PLA) code from the American Medical Association (AMA) for the IMMraytm PanCan-d test. The code will be effective on October 1, 2022. Immunovia is currently in process with the Centers of Medicare & Medicaid Services (CMS) to establish payment for IMMraytm PanCan-d with this PLA code which will be included in the 2023 CMS Clinical Lab Fee Schedule.
"We are very pleased that the AMA has approved a unique CPT PLA code for our IMMraytm PanCan-d test. This is an important step in our ongoing efforts to secure reimbursement for our test," says Philipp Mathieu, CEO and President of Immunovia AB.
The CPT codes offer doctors and health care professionals a uniform language for coding medical services and procedures. It is the most widely accepted medical nomenclature used in the US to report physician and healthcare professional services including laboratory tests under public and private health insurance programs.
PLA Codes are an addition to the CPT code set approved by the AMA CPT Editorial Panel. They are alpha-numeric CPT codes with a corresponding descriptor for laboratories or manufacturers that want to identify their test more specifically.
For more information, please contact:
Philipp Mathieu
CEO and President
Email: [email protected]
Tobias Bülow
Senior Director Investor Relations and Corporate Communications
Email: [email protected]
Tel: +46 736 36 35 74
The information was submitted for publication on July 5, 2022, 9:30 am CET.
About Immunovia
Immunovia AB is a diagnostic company with the vision to revolutionize blood-based diagnostics and increase survival rates for patients with cancer.
Our first product, IMMraytm PanCan-d is the only blood test currently available specifically for the early detection of pancreatic cancer. The test has unmatched clinical performance. Commercialization of IMMraytm PanCan-d started in August 2021 in the USA and IMMraytm PanCan-d is offered as a laboratory developed test (LDT) exclusively through Immunovia, Inc. For more information see: www.immunoviainc.com.
Immunovia collaborates and engages with healthcare providers, leading experts and patient advocacy groups globally to make this test available to all high-risk pancreatic cancer groups.
The USA, the first market in which IMMraytm PanCan-d is commercially available, is the world's largest market for the detection of pancreatic cancer with an estimated value of more than USD 4 billion annually.
Immunovia's shares (IMMNOV) are listed on Nasdaq Stockholm. For more information, please visit www.immunovia.com.
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https://news.cision.com/immunovia-ab/r/cpt-pla-code-for-the-immray--pancan-d-test-approved,c3596648
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SOURCE Immunovia AB
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