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Trovagene, Inc., Grants License for NPM1 Marker to Quest Diagnostics for Acute Myelogenous Leukemia

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Trovagene, Inc. (NASDAQ: TROV), a developer of transrenal molecular diagnostics, announced it has granted Quest Diagnostics, the world’s leading provider of diagnostic testing, information and services, a non-exclusive license to incorporate nucleophosmin protein (NPM1) into research and clinical testing services related to acute myelogenous leukemia (AML). Trovagene holds an exclusive worldwide license to US patent 8,222,370 and the corresponding group of U.S. and foreign patent applications around NPM. Terms of the agreement include upfront fees and royalty payments on an annual basis. Additional terms were not disclosed.

“Trovagene continues to expand patient access to the NPM1 marker worldwide,” said Charlie Rodi, Ph.D., chief technology officer for Trovagene. “Physicians need accurate tools to assess prognosis, select therapies and evaluate for bone marrow transplant. Use of this marker can help physicians more effectively treat patients with AML.”

AML is a clinically heterogeneous disease that affects patients worldwide. About 13,000 new cases a year occur in the U.S., and nearly 9,000 patients die from the disease annually. Chromosome analysis provides valuable prognostic information for physicians treating AML patients when abnormalities are present. However, in almost half of AML cases the chromosomes appear normal and provide no guidance for the physician. Many AML patients have mutations in the NPM1 gene. These patients have been shown to have more favorable outcomes. Testing for NPM1 mutations is recommended by the National Comprehensive Cancer Network, which sets clinical treatment standards for a wide variety of cancers.

Source: Trovagene