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MethylGene and Celgene Announce Precautionary Suspension of New Enrollments Into MGCD0103 Clinical Trials Print E-mail
23 Jul 2008

MethylGene to Host Conference Call Today at 5:00 p.m. Eastern Time

MONTREAL, QUEBEC, CANADA and SUMMIT, NJ, USA | July 23, 2008 | MethylGene Inc. (TSX:MYG) and Celgene Corporation today announced that, at the recommendation of a standing internal safety committee, the companies are temporarily suspending enrollment of new patients into clinical trials evaluating MGCD0103.

This voluntary precaution is being taken due to the observation of pericarditis or pericardial effusion in 19 patients out of approximately 400 patients treated to date. Approximately half of the reported cases have been deemed by investigators as unlikely to be drug related. It is not yet determined whether the potential signal is drug related due to confounding factors in these complex and late-stage cancer patients. Because the events tend to occur during the first cycle of treatment, patients currently enrolled in MGCD0103 clinical trials who have no signs or symptoms of the events are not affected by this temporary action and may continue in their respective studies.

The companies are working to fully communicate this precautionary measure to the appropriate investigators and regulatory agencies. Additionally, the companies are putting in place a series of steps moving forward to provide safe access to the clinical benefits of this promising therapy as soon as possible.

Conference Call Information

MethylGene will host a brief conference call to discuss events mentioned in this release. The call is scheduled for today, July 22nd, at 5:00 p.m. ET. MethylGene would like to invite all interested parties to participate by dialing 416-644-3419 or 1-800-595-8550 shortly before 5:00 p.m. ET. On the call from MethylGene will be:

Mr. Donald F. Corcoran, President and Chief Executive Officer

Dr. Jeffrey M. Besterman, Executive Vice President R&D and Chief Scientific Officer

Dr. Robert E. Martell, Vice President and Chief Medical Officer

A question and answer session will follow, at which time the operator will direct participants as to the correct procedure for submitting questions. A telephone replay of the conference call will also be available from July 22nd through July 28th, 2008. To access the replay, dial 416-640-1917 or 1-877-289-8525 and enter reservation number 21278982#.

About MGCD0103

MGCD0103 is an orally-administered, isoform-selective HDAC inhibitor. The compound is currently in multiple clinical trials: a Phase I trial in combination with Taxotere® for solid tumors; two Phase I/II trials, the first in combination with Vidaza® for hematological malignances and the second with Gemzar® for pancreatic cancer; several Phase II monotherapy trials in hematological malignancies and, more recently, a Phase II, three-arm combination trial with Vidaza in hematological malignancies. MGCD0103 has received orphan drug designation from the U.S. Food and Drug Administration (FDA) and has been designated an orphan medicinal product by the European Medicines Agency (EMEA) for the treatment of Hodgkin lymphoma and AML.

About MethylGene

MethylGene Inc. (TSX: MYG) is a publicly-traded, clinical stage, biopharmaceutical company focused on the discovery, development and commercialization of novel therapeutics for cancer. The Company's lead product, MGCD0103, is an oral, isoform-selective HDAC inhibitor presently in multiple clinical trials for solid tumors and hematological malignancies, including Phase II monotherapy and Phase I, Phase I/II and Phase II combination trials with Vidaza®, Gemzar® and Taxotere®. MGCD265 is an oral, multi-targeted kinase inhibitor targeting the c-Met, Tie-2, Ron and VEGF receptor tyrosine kinases and is in Phase I clinical trials for solid tumor cancers. In addition, MethylGene's preclinical programs include: MGCD290, an HDAC inhibitor used in combination with azoles for fungal infections, a kinase inhibitor program for ocular diseases, and a sirtuin inhibitor program for cancer. MethylGene's development and commercialization partners include Celgene Corporation, Taiho Pharmaceutical Co. Ltd., Otsuka Pharmaceutical Co. Ltd. and EnVivo Pharmaceuticals. Please visit our website at www.methylgene.com.

About Celgene

Celgene Corporation, based in Summit, New Jersey, is an integrated global biopharmaceutical company engaged primarily in the discovery, development and commercialization of novel therapies for the treatment of cancer and inflammatory diseases through gene and protein regulation. For more information, please visit the Company's website at www.celgene.com.

SOURCE: MethylGene Inc. and Celgene Corporation





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