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Classified in: Health, Science and technology, Business
Subject: FEA

Immunovia reiterates its road to reimbursement for the IMMraytm PanCan-d test


LUND, Sweden, April 22, 2021 /PRNewswire/ -- Immunovia is launching its IMMraytm PanCan-d test in the US as a Laboratory Developed Test (LDT) in Q2 2021. The company will explore a positive Medicare coverage determination for the IMMraytm PanCan-d test through the Local Coverage Determination (LCD) process.

The IMMraytm PanCan-d test will be performed at Immunovia Dx Laboratories in Marlborough, Massachusetts, and will be available to all patients in the US. In accordance with Medicare regulations, all Medicare billing will be conducted by Immunovia Dx Laboratories through the Medicare Administrative Contractor (MAC) that administers benefits in Massachusetts (National Government Services or NGS). Therefore, obtaining coverage from NGS would be sufficient for coverage of all Medicare-participating patients nationwide.

Patrik Dahlen, CEO Immunovia, stated "We believe that the IMMraytm PanCan-d test, intended as an aid in diagnosis in patients at high risk for developing pancreatic ductal adenocarcinoma (PDAC), meets the reasonable and necessary criteria for Medicare coverage."

Based on numerous interviews and working closely with experts on the subject, Immunovia concludes that if the IMMraytm PanCan-d test is used analogously to already-covered surveillance imaging modalities, and for the same high-risk population, then it is reasonable that both commercial payers and Medicare will view this use of the test as a "diagnostic" test rather than a "screening" test. Publications from the International Cancer of the Pancreas Screening (CAPS) Consortium, NCCN, ASCO and US Preventive Services Task Force (USPSTF) all recommend enrolling high-risk populations for pancreatic cancer into surveillance programs. More specifically, the high-risk population identified in the CAPS guidelines as eligible for pancreatic cancer surveillance overlaps almost completely with the population included in the groundbreaking PanFAM-1 clinical utility study of the IMMraytm PanCan-d test.

Diagnostics reimbursement expert Dr. David Parker, a Senior Vice President at Precision for Medicine, stated "Market research indicates that surveillance imaging of patients at high risk for pancreatic cancer is already routinely covered by payers, and is not considered as a screening application of the imaging modalities. Immunovia will be seeking coverage for the same surveillance use, in the same population. It seems highly unlikely that payers will view the IMMraytm PanCan-d test as a screening test, when they cover the clinical alternatives as diagnostic."

Immunovia will continue to execute focused US studies ? including PanFAM-1 ? to build the necessary evidence and dossiers, and to thereby establish clinical utility. The company's aim is to obtain coverage and reimbursement agreements with a majority of U.S. payers prior to year-end 2022.

For more information, please contact:

Patrik Dahlen, CEO Immunovia

Email: [email protected]

Tel: +46 73 376 76 64

About Immunovia

Immunovia AB is a diagnostic company that is developing and commercializing highly accurate blood tests for the early detection of cancer and autoimmune diseases based on Immunovia's proprietary test platform called IMMraytm. Tests are based on antibody biomarker microarray analysis using advanced machine-learning and bioinformatics to single-out a set of relevant biomarkers that indicate a certain disease. Thus, forming a unique "disease biomarker signature".

The company was founded in 2007, based on cancer studies and ground-breaking research in the Department of Immuntechnology at Lund University and CREATE Health Cancer Center, Sweden.

The first product, the IMMraytm PanCan-d test, is undergoing clinical evaluation in some of the world's largest clinical studies for pancreatic cancer, PanFAM-1, PanSYM-1 and PanDIA-1 and is currently in the final validation phase. The final validation study was completed in Q1 2021. Commercial testing will begin in Q2 after the accreditation of Immunovia Dx Laboratory in Marlborough, Massachusetts, USA.

The IMMraytm PanCan-d test will be the first blood-based test for early diagnosis of pancreatic cancer on the market, with a potential to significantly improve patient survival and outcome.

Immunovia Dx Laboratories located in Marlborough, Massachusetts, USA and Lund, Sweden will provide laboratory testing services in two accredited reference laboratories.

Immunovia's shares (IMMNOV) are listed on Nasdaq Stockholm. For more information, please visit www.immunovia.com.

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This information was brought to you by Cision http://news.cision.com

https://news.cision.com/immunovia-ab/r/immunovia-reiterates-its-road-to-reimbursement-for-the-immray--pancan-d-test,c3330934

The following files are available for download:

https://mb.cision.com/Main/13121/3330934/1405542.pdf

Press release (PDF)

 

SOURCE Immunovia AB


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