Genzyme files applications for approval of Mozobil in the US and Europe

Published: 19-Jun-2008
Regulatory

Genzyme Corporation has submitted marketing applications in both the US and the European Union for Mozobil (plerixafor), a product candidate intended to enhance mobilisation of hematopoietic stem cells for collection and subsequent autologous transplantation in patients with lymphoma and multiple myeloma.


Genzyme Corporation has submitted marketing applications in both the US and the European Union for Mozobil (plerixafor), a product candidate intended to enhance mobilisation of hematopoietic stem cells for collection and subsequent autologous transplantation in patients with lymphoma and multiple myeloma.

The company has requested priority review of its US application and, if granted, Mozobil could be approved by the end of this year. European approval is expected in 2009. Additional global applications in up to 60 countries are expected to follow.

Mozobil is designed to mobilise stem cells from the bone marrow into the bloodstream where they can be collected, making it more likely for a patient with certain types of cancers to receive a successful transplant.

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