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Clinical Trial Summary

The purpose of this study is to gather and evaluate additional safety data on the combination of midostaurin and standard of care for adult patients with newly diagnosed Fms-like tyrosine kinase receptor (FLT3) mutated Acute Myeloid Leukemia (AML) who are eligible for standard induction and consolidation chemotherapy and are without satisfactory treatment alternatives prior to the commercial availability* and reimbursement of midostaurin during the regulatory approval process


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT03114228
Study type Expanded Access
Source Novartis
Contact
Status No longer available
Phase

See also
  Status Clinical Trial Phase
Withdrawn NCT02829840 - Dose-Escalation Study of Ponatinib, a FLT3 Inhibitor, With and Without Combination of 5-Azacytidine, in Patients With FLT3-Mutated Acute Myeloid Leukemia (AML) Phase 1/Phase 2
Recruiting NCT03591510 - A Global Study of Midostaurin in Combination With Chemotherapy to Evaluate Safety, Efficacy and Pharmacokinetics in Newly Diagnosed Pediatric Patients With FLT3 Mutated AML Phase 2
Recruiting NCT05520567 - A Study of Gilteritinib, Venetoclax and Azacitidine as a Combined Treatment for People Newly Diagnosed With Acute Myeloid Leukemia Phase 1/Phase 2
Active, not recruiting NCT02310321 - A Study of ASP2215 in Combination With Induction and Consolidation Chemotherapy in Patients With Newly Diagnosed Acute Myeloid Leukemia. Phase 1/Phase 2