Pharma BD Deal Intelligence

Innovent Biologics, Inc. / Daiichi Sankyo Company, Limited

2026 · Licensing/Option · Complete

Daiichi Sankyo hands China commercialization of an approved FLT3 inhibitor to Innovent

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Innovent Biologics and Daiichi Sankyo entered an exclusive agreement for commercialization of VANFLYTA (quizartinib) in China. Innovent holds sole commercialization rights in China and leads market promotion, while Daiichi Sankyo remains responsible for development, manufacturing and supply. VANFLYTA is a FLT3 inhibitor approved in Japan, the United States and Europe for relapsed or refractory FLT3-ITD positive acute myeloid leukemia, and was approved in China in June 2026 in combination with standard cytarabine and anthracycline induction and cytarabine consolidation, and as maintenance monotherapy following consolidation chemotherapy, for newly diagnosed FLT3-ITD positive AML. VANFLYTA becomes the 20th product in Innovent's commercialized portfolio. Financial terms were not disclosed.

Key facts

Disease & market context

FLT3-ITD Positive Acute Myeloid Leukemia

Disease Overview

Acute myeloid leukemia with FLT3-ITD mutations carries a poor prognosis and high relapse risk. VANFLYTA (quizartinib) was approved in China in June 2026 in combination with standard cytarabine and anthracycline induction and cytarabine consolidation, and as maintenance monotherapy following consolidation, for newly diagnosed FLT3-ITD positive AML.

Deal timeline

Related deals — scored

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