EC approval for Blincyto in pediatric patients

29 August 2018
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US biotech major Amgen (Nasdaq: AMGN) has received the green light from the European Commission (EC) to start marketing Blincyto (blinatumomab) to a new patient group.

The bispecific CD19-directed CD3 T cell engager immunotherapy has been approved as a monotherapy for pediatric patients aged one year or older with Philadelphia chromosome-negative CD19 positive B-cell precursor acute lymphoblastic leukemia (ALL), which is refractory or in relapse after receiving at least two prior therapies or in relapse after receiving prior allogeneic hematopoietic stem cell transplantation.

This label expansion follows on from Blincyto’s initial EC approval in the adult patient group in 2015 and is based only on results from a Phase I/II study.

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