NEW YORK, October 29 /PRNewswire/ --

Xenomics, Inc., (Pink Sheets: XNOM; FWB:X37) announces that it has granted Asuragen, Inc. co-exclusive worldwide rights to incorporate NPM1 technology into Asuragen's molecular diagnostic products. Under the terms of this agreement, Asuragen will have the right to develop, manufacture and market products for the diagnosis, stratification and monitoring of patients with Acute Myeloid Leukemia (AML).

AML is a clinically heterogeneous disease with an estimated 13,500 new cases per year in the US and 200,000 worldwide. The disease subgrouping by karyotypic abnormalities indicates patient prognosis. However, in almost half of AML cases the karyotype appears normal and provides no guide for the physician. A recent discovery by Drs. Falini and Mecucci at the University of Perugia showed that many AML patients have mutations in the nucleophosmin (NPM1) gene, a favorable marker for clinical outcome. Xenomics holds exclusive rights to the discovery and has co-exclusively sub-licensed mutations of the NPM1 gene to Asuragen, for diagnostic test development. The results of such a test will help physicians select patients with a good prognosis of benefiting from intensive chemotherapy, while sparing others with a low probability of benefit from the toxic treatment.

The NPM1 mutation may also be used to monitor AML patients for residual disease during chemotherapy. Monitoring is typically performed every three months per patient. Patient monitoring may be a key factor in over 400 ongoing clinical AML trials listed by the National Cancer Institute.

"Xenomics is committed to expanding patient access to the NPM1 marker worldwide," said Dr. Samuil Umansky, Chief Scientific Officer of Xenomics, Inc. "With this disease, physicians need a rapid assessment of patient prognosis for effective use of chemotherapy. NPM1 provides an excellent test for monitoring the minimal residual disease and patient response to anti-tumor therapy."

"Adding NPM1 mutation testing to the treating physician's testing arsenal will enable physicians and patients to make more informed choices in the treatment of AML," said Rollie Carlson, President of Asuragen. "NPM1 testing complements Asuragen's current leukemia products (Signature(R) LTx RUO) and we continue in our dedication to bring leading edge leukemia diagnostic products such as NPM1 testing to the AML community."

About Xenomics, Inc.

Xenomics is a molecular diagnostics company that focuses on the development of DNA-based tests using Transrenal DNA (Tr-DNA). Xenomics' patented technology uses safe and simple urine collection and can be applied to a broad range of applications, including prenatal testing, tumor detection and monitoring, tissue transplantation, infectious disease detection, genetic testing for forensic identity determination, drug development, and research to counter bioterrorism. Scientists from Xenomics were the first to report that fragments of DNA from normal cell death cross the kidney barrier and can be detected in urine. The Company believes that its technology will open significant new markets in the molecular diagnostics field. Xenomics has three issued U.S. patents covering different applications of the technology for molecular diagnostics and genetic testing and a European patent for the Company's prenatal testing applications, and numerous pending patent applications. For more investor-specific information, including daily and historical Company stock quote data, recent news releases and an Investor Fact Sheet, please visit Xenomics is also listed on the Frankfurt Stock Exchange under the symbol XE7.

About Asuragen, Inc.

Asuragen is a fully integrated diagnostics company focused on molecular oncology and early detection of cancer, with emphasis on microRNA. Asuragen's current diagnostic product portfolio consists of Signature(R) Genetic Testing and Oncology Testing products, as well as industry leading controls and standards engineered using its patented Armored RNA(R) technology. Asuragen is dedicated to developing new technologies that will become cutting edge clinical products. In addition to being empowered with high level scientific expertise, Asuragen has a strong business infrastructure, GLP testing services and an established cGMP manufacturing facility that allow it to span the spectrum of discovery, testing, production and commercialization. For more information, please visit

Asuragen, Inc. 2150 Woodward St., Suite 100, Austin, T.X. 78744 PH: +1-512-681-5200 T: +1-877-777-1874 F: +1-512-681-5201

Forward-Looking Statements

Certain statements made in this press release are forward looking. Such statements are indicated by words such as "expect," "might," "should," "anticipate" and similar words indicating uncertainty in facts and figures. Although Xenomics believes that the expectations reflected in such forward-looking statements are reasonable, it can give no assurance that such expectations reflected in such forward-looking statements will prove to be correct. As discussed in Xenomics' Form 10-KSB as filed with the Securities and Exchange Commission on May 16, 2006 and its other periodic reports, actual results could differ materially from those projected in the forward-looking statements as a result of the following factors, among others: uncertainties associated with product development, the risk that Xenomics will not obtain approval to market its products, the risk that Xenomics' technology will not gain market acceptance, the risks associated with dependence upon key personnel, and the need for additional financing.

Xenomics Contact: David Robbins V.P., Product Development Xenomics, Inc. +1-908-489-9182 Asuragen Contact: Lori Brisbin Director of Marketing Asuragen, Inc. +1-512-681-5200 Web site:

David Robbins, V.P., Product Development, Xenomics, Inc., +1-908-489-9182,; or Lori Brisbin, Director of Marketing, Asuragen, Inc., +1-512-681-5200,