- Release Date: 05/04/16 12:05
- Summary: DIRECTOR: PEB: Confirmation of Director Appointment
- Price Sensitive: No
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PEB 05/04/2016 12:05 DIRECTOR NOT PRICE SENSITIVE REL: 1205 HRS Pacific Edge Limited DIRECTOR: PEB: Confirmation of Director Appointment 5 April 2016 CONFIRMATION OF DIRECTOR APPOINTMENT Pacific Edge Limited (PEB:NZX) has today advised that David Levison's appointment as a Director has been confirmed, effective as at 2 April 2016. David is a US-based Director, with an indepth knowledge and experience in the US healthcare market. He is currently CEO and a Director of CardioDx, a specialist molecular diagnostic company similar to Pacific Edge. David is highly respected within the industry and has in market experience in building a successful medical diagnostics company in the US. His understanding of commercial molecular diagnostic products in the US healthcare market, will be of great value to Pacific Edge as it looks to expand in this region. David will hold office until Pacific Edge's next Annual Shareholders' Meeting at which time he will offer himself for election by shareholders. The Board has determined that David Levison is an Independent Director, for the purposes of NZX Listing Rule 3.3.2. 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:00280360 For:PEB Type:DIRECTOR Time:2016-04-05 12:05:30
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