SI
SI
discoversearch

We've detected that you're using an ad content blocking browser plug-in or feature. Ads provide a critical source of revenue to the continued operation of Silicon Investor.  We ask that you disable ad blocking while on Silicon Investor in the best interests of our community.  If you are not using an ad blocker but are still receiving this message, make sure your browser's tracking protection is set to the 'standard' level.
Biotech / Medical : Diagnocure CUR

 Public ReplyPrvt ReplyMark as Last ReadFilePrevious 10Next 10PreviousNext  
To: Cal Gary who wrote (113)2/20/2001 2:14:49 PM
From: Mr. L. Neufeldt   of 132
 
Here's news release number two:

RIVIERA BEACH, Fla., Feb 20, 2001 (BUSINESS WIRE) -- AmeriPath, Inc. (NASD:PATH), the largest physician and laboratory company focused on providing anatomic pathology and cancer diagnostics, genomics, and healthcare information services, today announced that it will begin offering ImmunoCyt(TM), the first FDA-cleared cytopathology diagnostic test for the early detection of recurrent bladder cancer (transitional cell carcinomas) at its Center for Advanced Diagnostics located in Orlando, Fla.
ImmunoCyt(TM) is a highly sensitive, non-invasive test that allows urologists to detect antigens from tumors. Currently more than 300,000 people in the U.S. are being monitored for recurrence of bladder cancer and 55,000 new cases are detected annually. Bladder cancer is the sixth most common form of cancer in the United States.
"As part of our expanding test menu, we are proud to offer ImmunoCyt(TM) as another diagnostic resource for our clinicians and patients. We believe that it will become a valuable addition to the traditional diagnostic algorithm in helping urologists manage recurrent bladder cancer," said Randy Judd, M.D., Director of Special Technologies at AmeriPath's Center for Advanced Diagnostics.

"DAKO Corporation is pleased that AmeriPath and its Center for Advanced Diagnostics have added ImmunoCyt(TM) to their test menu. As one of the first commercial facilities to offer the test in the United States, they are leading the way in integrating this new tool into the current arsenal available to clinicians," said Douglas Sweet, DAKO's Vice President of Sales and Marketing. ImmunoCyt(TM) is licensed by DAKO Corporation from DiagnoCure, Inc. of Quebec City, Canada (TSE:CUR).

AmeriPath's Center for Advanced Diagnostics is a comprehensive esoteric reference laboratory offering a full array of traditional and molecular diagnostics for hematopoietic and solid tissue malignancies, including polymerase chain reaction (PCR), in situ hybridization, cytogenetics, flow cytometry, specialized immunohistochemistry, and minimal residual disease detection.

"AmeriPath, through our Center for Advanced Diagnostics, is committed to remaining on the cutting edge of pathology, molecular diagnostics, and genomics by continuing to research, implement and offer the latest diagnostic and prognostics tests and technologies available," added Dennis M. Smith, Jr., M.D., Senior Vice President and Medical Director for AmeriPath.

AmeriPath, Inc. is the nation's largest company focused on providing anatomic pathology and cancer diagnostics, genomics, and related healthcare information services to physicians, hospitals, national clinical laboratories and managed care organizations. The Company's 425 physicians provide medical services through 42 outpatient pathology laboratories, 224 hospital inpatient laboratories, and 64 outpatient surgery centers in 21 states.

The statements contained in this press release may include "forward-looking statements" which are based on management's current beliefs and expectations. Past performance is not necessarily indicative of future results. In addition, forward-looking statements - which are identified by words such as "may", "should", "believe", "expect", "anticipate", "estimate" and similar expressions - as well as any financial and operating estimates, forecasts and/or projections, are subject to a number of risks and uncertainties, many of which involve factors or circumstances which are beyond the Company's ability to control. These factors, risks and uncertainties could cause actual results to differ materially from historical results or those expected, estimated or anticipated. These include factors, risks and uncertainties relating to demand for pathology and related services, pricing, federal and state regulation (and compliance), reimbursement rates, government and third party payments, dependence upon pathologists, key personnel and contracts, competitive factors and technology. The forward looking statements included in this press release are made as of the date hereof, and the Company undertakes no obligation to update or revise any such statements, whether as result of new developments, new information or otherwise. Further information regarding risks, uncertainties and other factors that could affect the Company's financial or operating results, or which could cause actual results to differ materially from those expected or anticipated, are included in the Company's Form 10-K for the year ended December 31, 1999 and subsequent filings with the SEC.

Editor's Note: This release is also available at www.ameripath.com

CONTACT: AmeriPath, Inc., Riviera Beach
Gregory A. Marsh, 561/845-6211
or
Investor Relations:
AmeriPath, Inc.
Michelle D. Getty, 561/712-6260
invrel@ameripath.com

URL: www.businesswire.com
Today's News On The Net - Business Wire's full file on the Internet
with Hyperlinks to your home page.
Copyright (C) 2001 Business Wire. All rights reserved.

KEYWORD: FLORIDA
INDUSTRY KEYWORD: MEDICAL
DEVICES
PRODUCT
Report TOU ViolationShare This Post
 Public ReplyPrvt ReplyMark as Last ReadFilePrevious 10Next 10PreviousNext