Pharmion Corporation announced that the Agency for the Evaluation of Medicinal Products (EMEA) has accepted for review the Company's Marketing Authorization Application (MAA) for Vidaza for the treatment of Myelodysplastic Syndromes (MDS).
The US and European submissions for Vidaza were based upon a National Cancer Institute (NCI) sponsored phase III study for the treatment of MDS, conducted by Cancer and Leukaemia Group B (CALGB), and two supportive Phase II CALGB studies, which were also sponsored by the NCI.
Vidaza is the first drug approved in the United States for the treatment of MDS. Vidaza received a full approval for all five subtypes of MDS from the US Food and Drug Administration on May 19, 2004. These subtypes include: refractory anaemia (RA) or refractory anaemia with ringed sideroblasts (RARS) (if accompanied by neutropenia or thrombocytopenia or requiring transfusions), refractory anaemia with excess blasts (RAEB), refractory anaemia with excess blasts in transformation (RAEB-T), and chronic myelomonocytic leukaemia (CMMoL).
Vidaza has been granted Orphan Product Designation by the EMEA, which, if the MAA is approved, entitles the drug to ten years of market exclusivity for MDS in the European Union.
"We are pleased that the EMEA has accepted our application for Vidaza for filing, and we look forward to working closely with the EMEA in the coming months as we seek European regulatory approval for this treatment for this very serious disease," Judith A. Hemberger, executive vice president and chief operating officer of Pharmion said adding, "Through our recent experience with the approval and launch of Vidaza in the United States, we srecognize the real medical need that exists and hope to be able to provide a new treatment option for European physicians and their patients with Myelodysplastic Syndromes."
Azacitidine causes the death of rapidly dividing cells, including cancer cells that are no longer responsive to normal growth control mechanisms. In addition to this direct cytotoxic effect on abnormal cells in the bone marrow, azacitidine is member of a class of drugs in development known as "hypomethylating" or "demethylating" agents.
Methylation of DNA is a major mechanism regulating gene expression. Researchers have found that an increase in methylation of DNA can result in blockage of the activity of genes that regulate cell division and differentiation, known as "suppressor genes." With suppressor gene expression blocked, cell division becomes unregulated, allowing or promoting cancer. In in-vitro studies, researchers have found that azacitidine can reverse the methylation of DNA, which may restore normal function to genes that are critical for differentiation and proliferation.