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| | | ![]() EntreMed Granted Orphan Drug Designation for Panzem(R) (2ME2) In Glioblastoma ROCKVILLE, MD -- June 28, 2006 -- EntreMed, Inc.today announced that the U.S. Food and Drug Administration (FDA) has granted orphan drug designation for the Company's lead drug candidate, 2-methoxyestradiol (2ME2 or Panzem(R)), for the treatment of glioblastoma multiforme (GBM), an often fatal form of brain cancer. The FDA accepted EntreMed's application upon review of data from in vitro studies in glioma cell lines that demonstrate the antiproliferative activity of 2ME2. Additionally, results from in vivo studies in a preclinical model of glioblastoma demonstrate antitumor activity of 2ME2. In January 2006, EntreMed initiated a Phase 2 study in patients with glioblastoma multiforme at the Brain Tumor Center at Duke University Medical Center. Carolyn F. Sidor, M.D., EntreMed Vice President and Chief Medical Officer commented on the designation, "Glioblastoma is the most common malignant primary brain tumor representing approximately 12 to 15% of all brain tumors. Based on results from both preclinical experiments and mechanism-of-action studies, we believe that 2ME2 may be particularly well-suited for this patient population because these tumors are highly angiogenic and frequently harbor PTEN mutations, which result in high levels of HIF-1alpha protein. We have now received orphan drug designation for 2ME2 (Panzem(R)) in three cancer indications." Orphan drug is a designation by the Food and Drug Administration indicating a therapy developed to treat diseases that affect fewer than 200,000 persons in the United States. Sponsors of drugs granted orphan designation qualify for tax credit and marketing exclusivity incentives of the Orphan Drug Act. EntreMed received orphan drug designation previously for 2ME2 in the treatment of multiple myeloma (a type of blood cancer) and ovarian cancer. About Glioblastoma
SOURCE: EntreMed, Inc.
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