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www.fdanews.com/articles/97303-bioenvision-provides-evoltra-regulatory-update

Bioenvision Provides Evoltra Regulatory Update

August 16, 2007

Bioenvision announced an update on the status of its Marketing Authorization Application to the European Medicines Evaluation Agency (EMEA) to include a new indication for Evoltra (clofarabine) for the treatment of acute myeloid leukemia (AML) in elderly patients who have one or more of the following: adverse cytogenetics, secondary AML, ≥ 70 years old or significant co-morbidities and are therefore not considered suitable for intensive chemotherapy.
Bioenvision