
Innovent will push VANFLYTA deeper into China’s AML market as Daiichi Sankyo supplies the drug.
This is a meaningful China oncology commercialization move for both companies and a direct access story for a high-risk AML population.
AI reasoning
This is a meaningful China oncology commercialization move for both companies and a direct access story for a high-risk AML population.
Curated summary
Innovent Biologics and Daiichi Sankyo have entered an exclusive agreement for VANFLYTA commercialization in Mainland China. Daiichi Sankyo will handle development, manufacturing and supply, while Innovent gets sole commercialization rights and market promotion. VANFLYTA, or quizartinib, was approved in China in June 2026 for newly diagnosed FLT3-ITD-positive acute myeloid leukemia.
Supporting evidence
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Source news
Innovent and Daiichi Sankyo strike China deal for VANFLYTA commercialization
The partners have signed an exclusive agreement for quizartinib in Mainland China, where the drug was approved in June for FLT3-ITD-positive AML.



