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EPCT > SEC Filings for EPCT > Form 8-K on 4-Sep-2012All Recent SEC Filings

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Form 8-K for EPICEPT CORP


4-Sep-2012

Termination of a Material Definitive Agreement


Item 1.02 Termination of a Material Definitive Agreement.

On August 28, 2012, EpiCept Corporation (the "Company") received notice of termination of the License and Collaboration Agreement, dated November 19, 2003, with Myriad Genetics, Inc. (which subsequently transferred its interest to Myrexis, Inc. ("Myrexis")), Maxim Pharmaceuticals, Inc. and Cytovia, Inc., which was subsequently assigned to the Company (the "License Agreement"). The termination became effective on August 28, 2012. Myrexis has elected to terminate its efforts to develop and commercialize any product, including its drug candidate Azixa, in any major market as such products and markets are defined in the License Agreement. As a result of the termination of the agreement, all rights and licenses granted under the agreement by the Company to Myrexis will terminate and revert to the Company. The Company has 30 days from the date of the notice of termination to notify Myrexis of its interest, or lack thereof, in negotiation for the Myriad Technology License as set forth in the License Agreement.

Under the License Agreement, the Company licensed the MX90745 series of caspase-inducer anti-cancer compounds, including Azixa, to Myrexis. Under the terms of the agreement, the Company granted to Myrexis a research license to develop and commercialize any drug candidates from the series of compounds with a non-exclusive, worldwide, royalty-free license, without the right to sublicense the technology. Myrexis was responsible for the worldwide development and commercialization of any drug candidates from the series of compounds. The Company also granted to Myrexis a worldwide royalty bearing development and commercialization license with the right to sublicense the technology. In February 2012, Myrexis suspended development activities of all its preclinical and clinical programs in oncology and autoimmune diseases, and in May 2012 stated that it is focused on the identification, evaluation and acquisition of appropriate commercial-stage assets.


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