A Study of HYML-122 and Cytarabine in Patients With FLT3 Positive Relapsed or Refractory Acute Myeloid Leukemia (AML)

PHASE2RecruitingINTERVENTIONAL
Enrollment

18

Participants

Timeline

Start Date

March 29, 2022

Primary Completion Date

December 30, 2025

Study Completion Date

June 30, 2026

Conditions
Relapsed or Refractory Acute Myeloid Leukemia (AML)
Interventions
DRUG

HYML-122; cytarabine

HYML-122 is administered orally consecutive with 400mg bid or 600mg bid or dose adjusted by DMC judgement in each 28-day treatment cycle. cytarabine is administered by intravenous infusion with 100mg/m2 or dose adjusted by DMC judgement once daily on the first to 7th day of each treatment cycle. Upon completion of each 28-day treatment cycle, patients may continue to receive HYML-122 and cytarabine if they are benefit from the treatment and the toxicity is tolerable.

Trial Locations (1)

215006

RECRUITING

the First Affiliated Hospital of Soochow University, Suzhou

All Listed Sponsors
lead

Tarapeutics Science Inc.

INDUSTRY