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Tuesday, 18 November 2008 |
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IDM Pharma, Inc. has received a positive opinion from the Committee for Medicinal Products for Human Use (CHMP) of the European Medicines Agency (EMEA) and the recommendation to grant centralized marketing authorization for mifamurtide (L-MTP-PE), known as MEPACT(R) in Europe, for the treatment of patients with non-metastatic, resectable osteosarcoma. Final approval from the European Commission is expected in early 2009 once the recommendation has been adopted at the next CHMP meeting.
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