A Study of the Efficacy and Safety of Flumatinib in Patients With Newly Diagnosed Chronic Myeloid Leukemia in Chronic Phase.
- Conditions
- CML, Chronic Phase
- Interventions
- Registration Number
- NCT05353205
- Lead Sponsor
- Jiangsu Hansoh Pharmaceutical Co., Ltd.
- Brief Summary
It's a double-blind , randomized ,multi-center study. The purpose of this study is to explore the efficacy and safety of flumatinib 400mg once daily (QD) versus 600mg QD as the first line therapy in patients with chronic myleiod leukemia(CML) in chronic phase(CP).
- Detailed Description
This is a dose-optimization study of flumatinib in adult patient with newly diagnosed CML-CP. The objective of this study is to compare the efficacy and safety of flumatinib 400mg QD with that of 600mg QD. Eligible patients are randomized in a 1:1 ratio to receive either fluamtinib 400mg QD or flumatinib 600mg QD. Randomization is stratified based on Sokal risk score (\<0.8,0.8\~1.2,\>1.2). Patients will discontinue study therapy due to treatment failure, disease progression or intolerance to study medication or due to investigator's or participant's decision. The primary efficacy endpoint is the rate of early molecular response , as measured by RQ-PCR at 3 months. Hematologic response, molecular response and cytogenetic response will be assessed at baseline and a certain frequency after treatment, until study completion.
Recruitment & Eligibility
- Status
- RECRUITING
- Sex
- All
- Target Recruitment
- 200
- Signed informed consent form.
- Men or women aged more than or equal to (≥) 18 years, and less than (<) 75 years.
- ECOG performance status of 0-2.
- Patients with philadelphia chromosome positive chronic myeloid leukemia in chronic phase (Ph+ CML-CP) within 6 months of diagnosis.
- Adequate organ function.
- Men or women should be using adequate contraceptive measures throughout the study; Females should not be breastfeeding at the time of screening, during the study and until 6 months after completion of the study.
- Females must have evidence of non-childbearing potential.
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Known atypical CML or presence of additional chromosomal abnormalities.
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Known presence of the T315I mutation.
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Treatment with tyrosine kinase inhibitor(s) prior to randomization.
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Any treatment with anti-CML activity for longer than 2 weeks(exception of hydroxyurea or anagrelide) or hematopoietic stem cell transplantation prior to randomization .
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Prior treatment with splenectomy.
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Impaired cardiac function including any one of the following:
- Resting corrected QT interval (QTc) > 470 ms obtained from electrocardiogram (ECG), using the screening clinic's ECG machine and Fridericia's formula for QT interval correction (QTcF).
- Any clinically important abnormalities in rhythm, conduction, or morphology of the resting ECG.
- Any factors that increase the risk of QTc prolongation or risk of arrhythmic events,
- Left ventricular ejection fraction (LVEF) ≤ 50%.
- During screening period, ECG examination showed average heart rate <50 beats per minute.
- Myocardial infarction occurred within 12 months of randomization;
- Congestive heart failure occurred within 6 months of randomization;
- Uncontrollable angina.
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Stroke or transient ischemic attack within 6 months of randomization.
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Any severe or uncontrolled systemic diseases (i.e. uncontrolled hypertension or diabetes).
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Clinically severe gastrointestinal dysfunction that may affect drug intake, transport or absorption.
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The presence of active infectious diseases has been known prior to randomization
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History of significant congenital or acquired bleeding disorders unrelated to CML
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Inadequate other organ function.
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History of other malignancies.
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History of hypersensitivity to any active or inactive ingredient of flumatinib.
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Patients who are currently receiving treatment with any medications that have the potential to prolong the QT interval and the treatment cannot be either discontinued.
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Major surgery within 4 weeks of randomization.
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Any unresolved toxicities from prior therapy greater than Common Terminology Criteria for Adverse Events (CTCAE) Grade 1 within 4 weeks of randomization.
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Any disease or condition that, in the opinion of the investigator, would compromise the safety of the patient or interfere with study assessments.
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Judgment by the investigator that the patient should not participate in the study if the patient is unlikely to comply with study procedures, restrictions, and requirements.
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Flumatinib (400mg) Flumatinib mesylate tablets (400mg) Flumatinib 400mg QD Flumatinib (600mg) Flumatinib mesylate tablets (600mg) Flumatinib 600mg QD
- Primary Outcome Measures
Name Time Method Early molecular response(EMR) rate at 3 months 3 months Molecular response is assessed using BCR-ABL transcript levels and measured by realtime quantitative polymerase chain reaction(RQ-PCR). Early molecular response is defined as a ratio BCR-ABL/ABL ≤10% on the international scale (IS).
- Secondary Outcome Measures
Name Time Method MR4.0 rate at month 3,6,9 and 12 3, 6, 9 and 12 months MR4.0 is defined as BCR-ABL/ABL ≤0.01% on the international scale.
Complete hematologic response(CHR) rate at month 1,2,3,4,5,6,9 and 12 1,2,3,4,5,6,9 and 12 months Hematologic response will be assessed by complete blood count (CBC) and physical examination at each visit. CHR is defined as all of the following present:
1. white blood cell(WBC) count \<10×109/L
2. Platelet count \<450 ×109/L
3. Peripheral blood basophils \<5%
4. No blasts and no promyelocytes in peripheral blood
5. \< 5% myelocytes plus metamyelocytes in peripheral blood
6. No evidence of extramedullary disease, including no splenomegaly or hepatomegalyTime to first MMR up to 36 months Evaluate the time from the date of randomization to the date of first documented MMR during treatment.
Event-free survival (EFS) up to 36 months EFS is defined as the time from the date of randomization to the earliest occurrence of the following events: death due to any cause ; loss of CHR ,loss of PCyR ;loss of CCyR ; discontinuation of study treatment due to AE or treatment failure ; progression to AP/BC
Duration of CCyR up to 36 months Duration of CCyR is defined as the time from the date of first documented CCyR to the earliest date of loss of CCyR.
Major molecular response(MMR) rate at month 3,6,9 and 12 3, 6, 9 and 12 months Major molecular response is defined as a ratio BCR-ABL/ABL ≤0.1% on the international scale as measured by RQ-PCR.
Time to first CCyR up to 36 months Evaluate the time from the date of randomization to the date of first documented CCyR during treatment.
Progression-free survival (PFS) up to 36 months PFS is defined as the time from the date of randomization to the earliest occurrence of progression to AP/BC or death from any cause.
MR4.5 rate at month 3,6,9 and 12 3, 6, 9 and 12 months MR4.5 is defined as BCR-ABL/ABL ≤0.0032% on the international scale.
Complete cytogenetic response（CCyR）rate at month 3,6,9 and 12 3, 6, 9 and 12 months Cytogenetic response (CyR) is based on the prevalence of Ph+ cells in metaphase from bone marrow (BM) sample . CCyR is defined as 0% Ph+ metaphases in the bone marrow.
Duration of MMR up to 36 months Duration of MMR is defined as the time from the date of first documented MMR to the earliest date of loss of MMR.
Overall survival (OS) Frame:12 and 36 months OS is defined as the time from the date of randomization to the date of death from any cause.
Pharmacokinetics (PK) of HS-10096：Tmax Up to approximately 36 months Serum concentrations of HS-10096 will be collected and analyzed to evaluate the PK of HS-10096.Tmax is the time to reach maximum (peak) plasma drug concentration after dose administration (hr).
The incidence and severity of adverse events ((AE) up to 36 months Assessed by number and severity of adverse events as recorded on the case report form NCI CTCAE v5.0.
Trial Locations
- Locations (1)
Institute of Hematology and Oncology, Harbin The First Hospital
🇨🇳Harbin, Hei Longjiang, China