News & Events

ChemGenex Pharmaceuticals Limited (ASX:CXS) announced today that the European Medicines Agency ("EMEA") has determined that the Marketing Authorization Application ("MAA") for omacetaxine mepesuccinate for the treatment of chronic myeloid leukemia (CML) patients who have
failed treatment with imatinib and who have developed the Bcr-Abl T315I mutation is valid. Validation of the MAA indicates that ChemGenex's application, submitted on 29 October 2009, is complete and that the review process has begun. The filing is based on data from pivotal Study 202 where omacetaxine demonstrated clinical benefit for the treatment of T315I positive CML patients.

This additional regulatory milestone follows the acceptance earlier this month of a New Drug Application (NDA) by the U.S. Food and Drug Administration (FDA) for marketing approval for omacetaxine (filed under the trade name Omapro^TM) in the U.S.A.

"The submission and validation of this MAA shortly after our NDA submission and acceptance shows the commitment by ChemGenex to offer a treatment option to patients suffering from this life threatening condition" said Greg Collier, PhD, Chief Executive Officer and Managing Director. "This milestone marks another major accomplishment for ChemGenex this year, and we remain dedicated to expanding the use of omacetaxine within CML as well as with other leukemias."

Omacetaxine has received Orphan Drug designation from the EMEA and the FDA, and has received fast track status and Priority Review from the FDA. The MAA filing has been submitted in accordance with the centralized procedure and will be assessed by the EMEA. An opinion by the EMEA is expected in the fourth quarter of 2010. If approved, the marketing license will be valid simultaneously
in all EU Member States plus Iceland, Liechtenstein and Norway. Orphan Drug designation will give omacetaxine market exclusivity for a period of ten years.