Conditional European approval for Tecartus in mantle cell lymphoma

16 December 2020

Following a positive recommendation by the European Medicines Agency’s Committee for Medicinal Products for Human Use (CHMP) in October, the European Commission has now granted conditional marketing authorization for Tecartus (autologous, anti-CD19-transduced CD3+ cells; formerly KTE-X19).

The drug was developed by Kite, now a subsidiary of Gilead Sciences (Nasdaq: GILD) as a result of its $11.9 billion acquisition in 2017.

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