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Radient Pharmaceuticals Presented Two Abstracts at Gastrointestinal Cancers Symposium (ASCO) on Jan 21, 2012


1/23/2012 6:50:58 AM

TUSTIN, Calif. and SAN FRANCISCO, Jan. 23, 2012 /PRNewswire/ -- Radient Pharmaceuticals Corporation (OTCQX: RXPC) (OTCPK: RXPC), developer and marketer of the Onko-Sure® In-Vitro Diagnostic (IVD) cancer test, announced today that the two abstracts submitted and accepted for the 2012 Gastrointestinal Cancers Symposium (ASCO Conference), were presented. These abstracts are now available for viewing at ASCO.org and will be published in the 4th Supplement of Journal of Clinical Oncology in February 2012.

The conference was held on January 19-21, 2012 at the Moscone West Building in San Francisco, California. Dr. Afsaneh Motamed-Khorasani, the Director of Oncology at Radient Pharmaceuticals, presented the data in the two abstracts.

These abstracts were the results of a collaborative study in the United States that compared the combined use of Onko-Sure® with Carcinoembryonic Antigen (CEA), the routine blood biomarker for Colorectal Cancer (CRC), versus CEA alone. The clinical study included a total of 639 subjects. Radient Pharmaceuticals' proprietary Onko-Sure® cancer blood test combined with the CEA test were more effective for the detection of colorectal cancer compared to using the CEA test alone (an increase of 55% in the test sensitivity). Furthermore, the combined usage of Onko-Sure® and CEA in monitoring CRC recurrence showed a significant clinical advantage in terms of sensitivity (an increase of 35% in the test sensitivity compared to what CEA can provide).

The first abstract, entitled "A novel, cost-effective strategy for the screening of colorectal cancer with higher patience compliance" is available at the following link: http://www.asco.org/ASCOv2/Meetings/Abstracts?&vmview=abst_detail_view&confID=115&abstractID=88133. This study with 564 patients concluded that combining the Onko-Sure® cancer test and the CEA test for CRC screening shows a significant clinical advantage and this approach should improve the early stage diagnosis of CRC.

The second abstract is entitled "A new strategy for the early detection of colorectal cancer recurrence" and is available at: http://www.asco.org/ASCOv2/Meetings/Abstracts?&vmview=abst_detail_view&confID=115&abstractID=88123. This study with 75 patients concluded that the combined usage of the Onko-Sure® cancer test and CEA in monitoring of the CRC recurrence also shows a significant clinical advantage. Dr. Motamed-Khorasani concludes that "improvements observed in this study by this companion diagnostic approach combining CEA and DR-70 raises a strong potential for the utility of this combined test for screening of high risk patients for colorectal cancer specially in stages I and II where early diagnosis can make a big difference. The sensitivity of 58% is well acceptable for a simple, non-expensive blood test with high patient compliance as a screening test while CEA with 38% sensitivity cannot be used for screening. Furthermore, the sensitivity of this combined test for detection of CRC recurrences was at 75% in comparison to what CEA can offer (56%). The early detection of recurrence has important effects on patient treatment options and survival rate."

"A key element of our 2012 strategy is to share our findings with influential groups of specialists, such as the attendees in ASCO Conference. There were close to 3,000 attendees in this conference and we are pleased by the reception we received," said Douglas MacLellan, Chairman and CEO. "Our Onko-Sure® colorectal cancer test provides a simple, non-expensive test that is not only effective and cleared for the monitoring of CRC but in combination with other diagnostic markers (CEA) could be potentially used for screening of the high risk individuals for CRC. This will potentially reduce the number of hospitalizations and annual deaths due to CRC."

For additional information on Radient Pharmaceuticals Corporation and its products visit: www.radient-pharma.com or e-mail info@radient-pharma.com. For Investor Relations contact Paul Knopick at: pknopick@eandecommunications.com or 949-707-5365.

About Radient Pharmaceuticals:

Headquartered in Tustin, California, Radient Pharmaceuticals Corporation is dedicated to saving lives and money for patients and global healthcare systems through the deployment of its FDA-cleared In- Vitro Diagnostic Onko-Sure® cancer test kit for colorectal cancer treatment and recurrence monitoring. The Company's focus is on the discovery, development and commercialization of unique high-value diagnostic tests that will help physicians answer important clinical questions related to early disease state detection, treatment strategy, and the monitoring of disease progression or recurrence. To learn more about our Company, products, and potentially life-saving cancer test, visit www.radient-pharma.com.

Forward-Looking Statements:

Safe Harbor Statement under the Private Securities Litigation Reform Act of 1995: The statements contained in this document include certain predictions and projections that may be considered forward-looking statements under securities law. These statements involve a number of important risks and uncertainties that could cause actual results to differ materially including, but not limited to, the performance of joint venture partners, as well as other economic, competitive and technological factors involving the Company's operations, markets, services, products, and prices. With respect to Radient Pharmaceuticals Corporation, except for the historical information contained herein, the matters discussed in this document are forward-looking statements involving risks and uncertainties that could cause actual results to differ materially from those in such forward-looking statements.

Radient Contact:

Paul Knopick
E & E Communications
pknopick@eandecommunications.com
(Tel:) 949.707.5365

SOURCE Radient Pharmaceuticals Corporation



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