MBI Med Biogene Inc

VANCOUVER, BRITISH COLUMBIA--(Marketwired - Mar 7, 2014) - Med BioGene Inc. (TSX-VENTURE:MBI) today announced the publication in the Journal of Thoracic Oncology of data demonstrating a second, independent validation of the 15-gene signature to be marketed as GeneFx® Lung entitled "Validation of a Histology-Independent Prognostic Gene Signature for Early-Stage, Non-Small-Cell Lung Cancer Including Stage IA Patients." The study validated in a prospective and blinded manner the prognostic accuracy of the GeneFx Lung signature in an independent cohort of 181 early-stage (I and II) non-small-cell lung cancer (NSCLC) tumor specimens in different histologic subtypes.

GeneFx Lung is a proprietary gene expression-based test to improve upon staging for identifying those patients with early-stage NSCLC who, following surgical removal of their tumor, are at higher and lower risks of mortality. In an initial study published in the Journal of Clinical Oncology of patient specimens from the National Cancer Institute of Canada Clinical Trials Group JBR.10 trial, patients classified by GeneFx Lung as high risk benefited from adjuvant chemotherapy, and those classified as low risk did not benefit and may have experienced a detrimental effect from adjuvant chemotherapy. GeneFx Lung was subsequently validated in predicting patient mortality in four independent studies involving data from tumor specimens totaling 676 untreated early-stage NSCLC patients.

On April 15, 2011, MBI and Precision Therapeutics Inc. entered into a commercialization, license and research reimbursement agreement which provides to Precision exclusive global rights to develop and commercialize GeneFx Lung.

"We believe that the blinded, prospective validation results published in the Journal of Thoracic Oncology, along with the prior validation results published in the Journal of Clinical Oncology, establish that the use of GeneFx Lung will result in better-informed and more personalized treatment decisions and improve the selection of patients who may benefit from adjuvant chemotherapy", stated Erinn B. Broshko, Executive Chairman of MBI.

The study published in the Journal of Thoracic Oncology was led by Drs. Ming-Sound Tsao, Frances A. Shepherd and Sandy D. Der at the Princess Margaret Cancer Centre, University Health Network in Toronto, and included Dr. Igor Jurisica, Jenna Sykes, Melania Pintilie, Dr. Chang-Qi Zhu, Dr. Dan Strumpf and Ni Liu.

The publication in the Journal of Thoracic Oncology can be assessed online (http://journals.lww.com/jto/Abstract/2014/01000/Validation_of_a_Histology_Independent_Prognostic.9.aspx).

The initial publication in the Journal of Clinical Oncology can also be assessed online (http://jco.ascopubs.org/content/early/2010/09/07/JCO.2009.26.4325.abstract) as can the independent editorial (http://jco.ascopubs.org/cgi/doi/10.1200/JCO.2010.31.0144) from Drs. Yang Xie and John D. Minna of the Hamon Center for Therapeutic Oncology Research and Simmons Cancer Center, University of Texas Southwestern Medical Center.

About Precision Therapeutics

Precision Therapeutics, a leading life science company based in Pittsburgh, Pennsylvania, is dedicated to improving the outcomes of cancer patients by providing personalized medicine solutions that aim to increase quality of life and cancer survival rates. Precision offers a portfolio of products developed to help guide physicians and patients with difficult clinical decisions throughout the continuum of cancer care.

Precision currently markets a number of tests through its CLIA-certified laboratory, including ChemoFx®, BioSpeciFx® and GeneFx® Colon.

For more information on Precision, please visit www.precisiontherapeutics.com.

About Med BioGene

MBI is a life science company based in Vancouver, British Columbia that is currently focused on managing the license and rights to GeneFx Lung. MBI's common shares are listed for trading on the TSX Venture Exchange.

For more information on MBI, please visit www.medbiogene.com.

The TSX Venture Exchange does not accept responsibility for the adequacy or accuracy of this release.

Certain statements in this press release contain forward-looking statements and information ("forward-looking statements") under applicable United States and Canadian securities legislation. Words such as "anticipates," "believes," "estimates," "expects," "intends," "may," "plans," "projects," "will," "would" and similar expressions are intended to identify forward-looking statements, although not all forward-looking statements contain these identifying words. Forward looking statements include, but are not limited to, that with respect to the timing, completion and/or results of clinical trials or studies, the timing for commercialization of any products, future profits, future product revenues, future shareholder value, future operations and plans, the completion and use of proceeds from transactions or financings and the prospects for negotiating partnerships or collaborations and their timing. These forward-looking statements are only a prediction based upon the party's current expectations, and actual events or results may differ materially. A party may not actually achieve the plans, intentions or expectations disclosed in its forward-looking statements. Forward-looking statements are subject to known and unknown risks and uncertainties and are based on uncertain assumptions that could cause a party's actual results and the timing of events to differ materially from those anticipated in such forward-looking information. You are cautioned not to place undue reliance on these forward-looking statements, which speak only as of the date of this press release. A party's forward-looking statements do not reflect the potential impact of any future partnerships, collaborations, acquisitions, mergers, dispositions, joint ventures or investments that that party may make. All forward-looking statements are qualified in their entirety by this cautionary statement and a party undertakes no obligation to revise or update any forward-looking statements as a result of new information, future events or otherwise after the date of this press release, other than as required by applicable law. Certain information included in this press release in respect of Precision and its scientific, clinical and/ or commercialization efforts have been provided to MBI by Precision. MBI may not have been able to confirm the accuracy of such information and you should not place undue reliance on any such information, including any information regarding Precision that would constitute forward-looking information. A redacted copy of the commercialization agreement, as amended, between Precision and MBI may be found at www.sedar.com. Each trademark, trade name or service mark of any entity appearing in this news release belongs to its holder.

Med BioGene Inc.Erinn B. BroshkoExecutive Chairman(800) 641-3593ebroshko@medbiogene.comwww.medbiogene.com

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