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Phase 3
Development Phase
0
Upcoming Catalysts
0
Historical Events
1
Regulatory Approvals
No catalyst events have been recorded for this drug yet.
0 competitors in FLT3-mutated Acute Myeloid Leukemia
View Full LandscapeTarget Indication
FLT3-mutated Acute Myeloid Leukemia
Clinical Trial
NCT03591510Last updated: 2/10/2026
No patent data available. Pre-approval drugs may not have Orange Book listings.
Rydapt
Rydapt is indicated: in combination with standard daunorubicin and cytarabine induction and high dose cytarabine consolidation chemotherapy, and for patients in complete response followed by Rydapt single agent maintenance therapy, for adult patients with newly diagnosed acute myeloid leukaemia (AML) who are FLT3 mutation positive (see section 4.2); as monotherapy for the treatment of adult patients with aggressive systemic mastocytosis (ASM), systemic mastocytosis with associated haematological neoplasm (SM AHN), or mast cell leukaemia (MCL).