Update On Komet 001 Identifying The Optimal Dose Of Ziftomenib For Patients With R R Aml

Komet 001 Demonstrates Efficacy Of Ziftomenib For Patients With R R For Questions: Media Contact: Michelle McCourt (650) 467-6800 Advocacy Contact: Lily Rose Atherton (202) 713-0083 Investor Contacts: Loren Kalm (650) 225-3217 Bruno Eschli (+4161 68-75284) – Results from KOMET-001 registration-directed trial of ziftomenib in R/R NPM1-m AML patients selected for oral presentation on Monday, June 2nd – – Encore presentation planned at EHA 2025

Komet 001 Demonstrates Efficacy Of Ziftomenib For Patients With R R Based on data from the KOMET-001 trial, the US Food and Drug Administration (FDA) granted breakthrough designation for the therapy last year for relapsed/refractory (r/r) NPM1-mutant (NPM1-m) AML The full data analyses from the KOMET-001 trial of ziftomenib in R/R NPM1 -m AML patients have been selected for oral presentation on Monday, June 2nd at the 2025 American Society of Clinical Kura Oncology and Kyowa Kirin have announced that an abstract detailing the results of the KOMET-001 trial of ziftomenib for patients with relapsed/refractory NPM1-mutant acute myeloid leukemia Key Takeaways Ziftomenib targets relapsed/refractory AML with NPM1 mutations, a condition with high relapse rates and poor survival outcomes The drug has received breakthrough therapy, fast track,

Komet 001 Demonstrates Efficacy Of Ziftomenib For Patients With R R Kura Oncology and Kyowa Kirin have announced that an abstract detailing the results of the KOMET-001 trial of ziftomenib for patients with relapsed/refractory NPM1-mutant acute myeloid leukemia Key Takeaways Ziftomenib targets relapsed/refractory AML with NPM1 mutations, a condition with high relapse rates and poor survival outcomes The drug has received breakthrough therapy, fast track, KOMET-001 trial met its primary endpoint for ziftomenib in R/R NPM1-mutant AML, with statistically significant CR and CRh rates Kura plans to submit an NDA for ziftomenib in Q2 2025 and initiate Kura Oncology, Inc May 22, 2025, 5:30 PM ET – Results from KOMET-001 registration-directed trial of ziftomenib in R/R NPM1 -m AML patients selected for oral presentation on Monday, June 2nd –
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