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Gilead/Kite’s Tecartus Moves Into Leukemia With Second US Indication

 
• By Joseph Haas

New indication for second-line-plus acute lymphoblastic leukemia means Tecartus will compete with Novartis’s Kymriah, although the Gilead/Kite product is approved for older patient base.

3d illustration of immune system T cells attacking cancer cells (CAR T-cell therapy) - Illustration
Kite obtains its second FDA approval for cell therapy Tecartus

With the second US Food and Drug Administration approval for its CAR-T therapy Tecartus and the company’s first approval in a leukemia setting, Kite Pharma, Inc. CEO Christi Shaw said the Gilead Sciences, Inc. cell therapy subsidiary is ready to look ahead to second priorities now that the initial priority of a full-fledged cell therapy portfolio is growing more substantial.

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Pipeline Watch is a weekly snapshot of selected late-stage clinical trial events and approvals announced by pharmaceutical and biotech companies at medical and industry conferences, in financial and company presentations, and in company releases and statements.

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