- Release Date: 29/02/16 09:40
- Summary: GENERAL: PEB: PE gains access to Veterans Administration in USA
- Price Sensitive: No
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PEB 29/02/2016 09:40 GENERAL NOT PRICE SENSITIVE REL: 0940 HRS Pacific Edge Limited GENERAL: PEB: PE gains access to Veterans Administration in USA 29 February 2016 PACIFIC EDGE SIGNS FEDERAL SUPPLY SCHEDULE AGREEMENT The USA subsidiary of global cancer diagnostics company, Pacific Edge Limited (NZX:PEB), has signed a Federal Supply Schedule (FSS) agreement with Veterans Administration, which will allow the company to market its innovative, non-invasive bladder cancer detection technology, Cxbladder, to the Veterans Administration (VA), the nation's largest integrated health care system. The FSS contract will provide access to Cxbladder for the 8.8 million veterans currently enrolled in the VA across 1700 sites. In addition, the contract also provides access to Cxbladder tests at the 150 US Department of Defense (DOD) facilities across the United States. Chief Executive of Pacific Edge, David Darling, said: "This is an exciting development for Pacific Edge in the United States and another significant commercial milestone for our company. The VA is one of our targeted three large customers for this market and could eventually become one of our largest customers in the USA. It is a separately funded federal program for veterans and their families and is recognised as a large and unique organisation. This contract adds to our commercial momentum in the United States and increases our penetration of this key market. "The FSS contract award is a lengthy and iterative process. Following this signing of the agreement, the VA will issue the contract award documentation and we will begin engaging with the key stakeholders within the many VA and DOD centers to ensure that Cxbladder is available to physicians and their patients." The USA sales force has recently increased to 18 dedicated sales executives operating in key geographic regions, who will now be able to work with the VA and DOD facilities and their healthcare providers to secure access to Cxbladder. Pacific Edge launched commercial operations in the United States, the world's largest healthcare market, in mid-2013. Laboratory through-put and revenue are tracking to the company's expectations following an active direct sales and marketing program to clinicians and healthcare organisations. Pacific Edge will continue to develop and commercialise its portfolio of cancer detection tests with a view to initially commercialising those technologies in New Zealand, followed by the USA and other markets. Further developments of the Cxbladder technology are underway, with a third test, Cxbladder Monitor, to be released in the United States this year, following its launch in New Zealand in December 2015. Cxbladder Predict is planned for launch in late 2016. ENDS For more information contact: David Darling Chief Executive Officer, Pacific Edge Ltd, P: +64 (3) 479 5800 OVERVIEW www.pacificedge.co.nz www.pacificedgedx.com Pacific Edge Limited (NZX: PEB) is a New Zealand publicly listed, cancer diagnostic company specialising in the discovery and commercialisation of diagnostic and prognostic tests for better detection and management of cancer. The company is developing and commercialising its range of Cxbladder bladder cancer tests globally through its wholly owned central laboratories in New Zealand and the USA. The company's products have been tested and validated in international multi-centre clinical studies. Pacific Edge has two proprietary, novel, accurate, molecular diagnostic products in-market providing actionable results, and better detection and management of urothelial cancer. Cxbladder Detect is available through the company's dedicated CLIA certified laboratories for customers in New Zealand, Australia and the USA. Cxbladder Triage is available in New Zealand and Australia. Cxbladder Monitor launched in New Zealand in December 2015 and is anticipated being available in the US in 2016. ABOUT Cxbladder Triage www.cxbladder.com Cxbladder Triage combines the power of the genomic biomarkers with additional phenotypic and clinical risk factors to accurately identify patients with haematuria who have a low probability of bladder cancer and may not require a more extensive urological evaluation. Cxbladder Triage is a tool for use by clinicians and physicians in primary evaluation of patients with hematuria and is intended to reduce the need for an expensive and invasive work-up in patients who have a low probability of having urothelial carcinoma. ABOUT Cxbladder Detect www.cxbladder.com Cxbladder Detect enables the non-invasive detection of bladder and other urinary tract cancers from a small volume of a patients' urine. Cxbladder Detect was launched in 2013 in the USA and is commercially available in New Zealand, Australia and the USA as a Laboratory Developed Test (LDT) from the company's CLIA certified laboratories. Cxbladder Detect provides physicians and clinicians with a quick, cost effective and accurate measure of the presence of the cancer as an effective adjunct to cystoscopy. ABOUT Cxbladder Monitor www.cxbladder.com Cxbladder Monitor, the third test in the Cxbladder portfolio for urologists, is a proprietary, non-invasive, molecular diagnostic test that combines genomic biomarkers measured from a small quantity of a patient's urine, with patient specific clinical factors to better monitor bladder cancer patients for recurrence. Bladder cancer has a recurrence rate of 50-80% and requires life-long surveillance. Cxbladder Monitor accurately identifies patients with a prior history of urothelial cancer (UC) whose Cxbladder Monitor score shows that they have a low probability of recurrent urothelial carcinoma. Cxbladder Monitor is designed to be used as the preferred adjunct test to cystoscopy in the management of patients for ongoing evaluation of recurrent bladder cancer. Refer to www.cxbladder.com for more information. End CA:00278479 For:PEB Type:GENERAL Time:2016-02-29 09:40:46
Ann: GENERAL: PEB: PE gains access to Veterans Administration in USA
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