Study of Crenolanib vs Midostaurin Following Induction Chemotherapy and Consolidation Therapy in Newly Diagnosed FLT3 Mutated AML
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- STATUS
- Recruiting
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- End date
- Nov 25, 2024
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- participants needed
- 510
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- sponsor
- Arog Pharmaceuticals, Inc.
Summary
A phase III randomized multi-center study designed to compare the efficacy of crenolanib with that of midostaurin when administered following induction chemotherapy, consolidation chemotherapy and bone marrow transplantation in newly diagnosed AML subjects with FLT3 mutation. About 510 subjects will be randomized in a 1:1 ratio to receive either crenolanib in addition to standard first line treatment of AML (chemotherapy and if eligible, transplantation) (arm A) or midostaurin and standard treatment (arm B). Potentially eligible subjects will be registered and tested for the presence of FLT3 mutation. Once the FLT3 mutation status is confirmed and additional eligibility is established, subject will be randomized and enter into the treatment phase.
Details
| Condition | Newly Diagnosed FLT3 Mutated AML |
|---|---|
| Treatment | cytarabine, crenolanib, Midostaurin, Duanorubicin |
| Clinical Study Identifier | NCT03258931 |
| Sponsor | Arog Pharmaceuticals, Inc. |
| Last Modified on | 13 February 2022 |
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