The purpose of this study is to assess if adding revumenib to standard chemotherapy improves outcomes in participants with AML with certain genetic mutations compared to chemotherapy alone. The study will also assess the safety of adding revumenib to chemotherapy.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Enrollment
468
Clinical Trial Site
Batumi, Adjara, Georgia
RECRUITINGClinical Trial Site
Tbilisi, Georgia
RECRUITINGClinical Trial Site
Tbilisi, Georgia
RECRUITINGEvent Free Survival
Time frame: Up to 2 years
Measurable Residual Disease Complete Remission Rate
Time frame: Up to 2 years
Overall Survival
Time frame: Up to 5 years
Rate of Complete Remission
Time frame: Up to 2 years
Overall Response Rate
Time frame: Up to 2 years
Duration of Complete Remission
Time frame: Up to 2 years
Duration of Composite Complete Remission
Time frame: Up to 2 years
Duration of Response
Time frame: Up to 2 years
Number of Participants with a Treatment-emergent Adverse Event
Time frame: Up to 2 years
Change from Baseline in Patient-reported Fatigue Questionnaire Scores
Time frame: Up to 2 years
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.
Clinical Trial Site
Seoul, South Korea
RECRUITINGClinical Trial Site
Seoul, South Korea
RECRUITING