Ignite Creation Date:
2025-12-24 @ 10:58 PM
Ignite Modification Date:
2026-01-02 @ 1:38 PM
Study NCT ID:
NCT06387069
Status:
RECRUITING
Last Update Posted:
2025-08-14
First Post:
2024-04-16
Is NOT Gene Therapy:
True
Has Adverse Events:
False
Brief Title:
A Study to Evaluate HMPL-306 in Patients With IDH1or IDH2-mutated Acute Myeloid Leukemia
Sponsor:
Hutchmed
Organization:
Study Overview
Official Title:
A Multicenter, Randomized, Open-Label, Phase III Clinical Study to Evaluate the Efficacy and Safety of HMPL-306 vs. Salvage Chemotherapy Regimens in Patients With IDH1- and IDH2-mutated Relapsed/Refractory Acute Myeloid Leukemia (R/R AML)
Status:
RECRUITING
Status Verified Date:
2025-08
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
This study is a multicenter, randomized, open-label, phase III clinical study (RAPHAEL) to evaluate the efficacy, safety, and PK of HMPL-306 versus salvage chemotherapy in patients with R/R AML harboring IDH1 and IDH2 mutations.
Detailed Description:
Study Overview This is a multicenter, randomized, open-label, phase III clinical study to evaluate the efficacy, safety, and PK of HMPL-306 versus salvage chemotherapy in patients with IDH1- and IDH2-mutated R/R AML (RAPHAEL).
The study is open-label, and all patients will be screened centrally to determine their IDH mutation status, and based on the screening results, the patients will be assigned to the corresponding IDH1 and IDH2 cohorts of this registration study. Patients with both IDH1 and IDH2 mutations be assigned to the IDH2 cohort. The study consists of divided into two cohorts. Patients with R/R AML harboring IDH1-R132 mutation will be included in Cohort 1, and patients with R/R AML harboring IDH2-R140, R172 mutations will be included in Cohort 2. The two cohorts will be designed independently, analyzed separately, and subjected to statistical hypothesis testing separately. Patients in both cohorts will be randomly assigned according to the central randomization system (IWRS) in a 1:1 ratio into the experimental group and the control group. Patients in the experimental group will receive HMPL-306 monotherapy at the following dose: 250 mg once daily (QD) (first cycle, C1) + 150 mg QD \[starting from the second cycle (C2)\]; patients in the control group will receive salvage chemotherapy (1 of 4), including 4 different treatment regimens: Two intensive regimens (EA± Mitox regimen and FLAG ± Ida regimen) and two non-intensive regimens (azacitidine and LoDAC). Prior to randomization, the investigator will pre-select a salvage chemotherapy regimen based on the patient's condition, and randomization will be stratified according to patients' response to prior first-line therapy (relapse within 6 months after allogeneic HSCT, relapse after 6 months after allogeneic HSCT, primary refractory without HSCT, relapse within 6 months after achieving CR/CRh without HSCT, or relapse after 6 months after achieving CR/CRh without HSCT) and the intensity of the pre-selected chemotherapy regimen (intensive chemotherapy or weak chemotherapy).
After the patients sign the pre-screening informed consent form (ICF), pre-screening (genetic testing) will be performed to determine IDH mutation status for subsequent enrollment cohort, and if a patient wants to know about RAS or FLT3 mutation status, local testing can be used to clarify the latest RAS or FLT3 hotspot mutation. Patients who meet the inclusion criteria of this study will be randomized to the experimental group or the control group to receive treatment in 28-day cycles until one of the following conditions occurs: Treatment failure \[refer to the Guidelines for Clinical Development of New Drugs for Acute Myeloid Leukemia issued by the Center for Drug Evaluation (CDE)\]. The definition of "treatment failure" is recommended as: Treatment failure occurs when CR or CRh/CRi is not achieved after 2 cycles of treatment per protocol using the regimens for the intensive chemotherapy group. When using the regimens for the weak chemotherapy group and the experimental group, treatment failure occurs if CR or CRh/CRi is not achieved after 4 cycles of treatment, i.e., disease progression/relapse, death, unacceptable toxicity, receiving new anti-tumor therapy, judgment by the investigator that the patient no longer obtains clinical benefit from treatment, withdrawal from the study by the patient or his/her legally acceptable representative, loss to follow-up, or end of the study occurs, whichever occurs first (The treatment duration of EA±Mitox regimen and FLAG±Ida regimen in the chemotherapy group will be adjusted according to the actual medication, and a maximum of two treatment cycles will be used).
Crossover is not allowed for patients with progressive disease in the control group and the experimental group, and patients in the control group will not be allowed to crossover to other salvage regimens.
The information on treatment groups is as follows (same for both cohorts):
The experimental group: Patients treated with HMPL-306 monotherapy:
\- The dose of HMPL-306 is 250 mg QD (C1) + 150 mg QD (starting from C2), continuous, PO, in 28-day treatment cycles.
The control group: Patients treated with one of the following regimens, and the regimen will be determined by the investigator on a case-by-case basis:
* EA±Mitox regimen: Etoposide Injection 100 mg/m2, Cytarabine Injection 100-150 mg/m2, and Mitoxantrone Injection 8 mg/m2, QD, intravenous (IV) administration for 5 consecutive days (Days 1-5). (In the case that Mitoxantrone Injection is not accessible, a regimen containing mitoxantrone liposome can be used, specifically: Mitoxantrone liposome + cytarabine + etoposide regimen: Mitoxantrone liposome 24-32 mg/m2, Day 1; Cytarabine 100-200 mg/m2, Day 1 to Day 7; and Etoposide 100 mg/m2, Days 1-5). The regimen can be used with or without mitoxantrone, which can be determined by the investigator based on the actual condition of the patient.
* FLAG±Ida regimen: G-CSF Injection 300 mcg/m2, QD subcutaneous administration for 5 consecutive days (Days 1-5); Fludarabine Injection 30 mg/m2, QD IV for 5 consecutive days (Days 2-6); Cytarabine Injection 1000-2000 mg/m2, QD IV for 5 consecutive days (Days 2-6); and Idarubicin Injection 10 mg/m2, QD IV for 3 consecutive days (Days 2-4). This regimen can be used with or without Ida, which can be determined by the investigator based on the actual condition of the patient. After the end of chemotherapy administration, the investigator will determine whether it is necessary to continue the administration of G-CSF, and if necessary, retreatment with G-CSF is allowed until absolute neutrophil count (ANC) \> 0.5x109/L.
* LoDAC: Cytarabine Injection 20 mg every 12 hours, subcutaneous or IV for 10 consecutive days (Days 1-10).
* Azacitidine: Azacitidine Injection 75 mg/m2, QD, subcutaneous or IV for 7 consecutive days (Days 1-7).
Study Period:
The study includes pre-screening period, screening period, treatment period and follow-up period \[including end of treatment (EOT) follow-up, safety observation follow-up, EFS follow-up, and OS follow-up\].
The pre-screening period is defined as the period from signing the pre-screening ICF to obtaining the IDH1 and IDH2 mutation testing reports. For patients without previous IDH1 or IDH2 testing reported, specimens should be sent to the central laboratory for IDH1 and IDH2 mutation testing and other companion gene testing after signing the pre-screening ICF and prior to screening. Patients with a previously reported positive IDH1 and/or IDH2 mutation test may proceed directly to screening without pre-screening if approved by the investigator. The results confirmed by the central laboratory are required for enrollment.
The screening period is defined as the period from signing the main screening ICF to Cycle 1 Day 1 pre-dose.
Treatment period is defined as the period from the first dose to EOT. EOT Follow-up: Patients with EOT need to return to the site for EOT follow-up within 1-7 days after discontinuing treatment, or before starting other anti-tumor therapy, whichever occurs first.
Safety Observation Follow-up: Patients with EOT need to return to the site for Safety Observation Follow-up within 30 (±7) days after the last dose of study drug treatment or before starting other anti-tumor therapy, whichever occurs first.
EFS Follow-up: Patients with EOT (except for EOT due to disease progression/relapse) will be advised to remain in the study for EFS follow-up, and patients without medication after randomization will also be advised for EFS follow-up, from the day of entering EFS follow-up, and then every 8 weeks until disease progression/relapse, death, withdrawal by the patient or his/her legally acceptable representative, patient lost to follow-up, or end of study, whichever occurs first. Subsequent new transplant conditioning regimens or new anti-tumor treatment regimens will be documented during EFS follow-up.
OS Follow-up: Patients who have been randomized and have completed EFS follow-up (and who have EOT due to disease progression/relapse) will receive OS follow-up every 8 weeks from the date they enter OS follow-up until death, withdrawal by the patient and his/her legally acceptable representative, loss to follow-up, or end of study, whichever occurs first. If a patient withdraws from treatment and not from the entire study, EFS and OS data collection will be continued.
End of Study Inconsistent time of end of study is allowed between the two cohorts. The end of study for each cohort is defined as the time when the target number of OS events for the final analysis is reached in the cohort. The actual duration of study for each cohort will depend on the actual enrollment rate, dropout rate, and the length of median OS in each group.
Efficacy Assessment(s) Efficacy evaluation will be based on modified 2022 European Leukemia Net (ELN) criteria. Efficacy assessment will be performed once for each of the first 6 cycles of study drug treatment (i.e., C2D1, C3D1, C4D1, C5D1, C6D1, C7D1) and every 2 cycles after 6 cycles of treatment (i.e., C9D1, C11D1, C13D1, ......); Efficacy assessments will also be performed at the Safety Observation Follow-up and each EFS Follow-up.
Safety Assessment(s) All adverse events (AEs) will be graded according to the National Cancer Institute Common Terminology Criteria for Adverse Events (NCI CTCAE) version 5.0. AEs will be coded using Medical Dictionary for Regulatory Activities (MedDRA). The number and incidence of treatment-emergent adverse events (TEAEs) will be summarized by system organ class and preferred term.
All the serious adverse events (SAEs) related with the study procedure will be collected from the date of the signing of informed consent form for pre-screening to the date of the signing of master informed consent form; all the SAEs will be collected from the date of the signing of master informed consent form to the date when the first dose is given; all AEs/SAEs will be collected from the date when the first dose is given to 30 days after the last dose is given, or the date when a new anti-tumor therapy is started, whichever occurs first (If HSCT is performed, safety data on and after HSCT treatment will no longer be collected; If a patient experiences disease recurrence after HSCT and is re-enrolled to receive HMPL-306 treatment, the adverse events after HSCT need to be collected); SAEs confirmed by the investigator to have a reasonable possibility of correlation with the study drug will be collected 30 days after the last dose or after the start of a new antitumor therapy, whichever occurs first.
The study is open-label, and all patients will be screened centrally to determine their IDH mutation status, and based on the screening results, the patients will be assigned to the corresponding IDH1 and IDH2 cohorts of this registration study. Patients with both IDH1 and IDH2 mutations be assigned to the IDH2 cohort. The study consists of divided into two cohorts. Patients with R/R AML harboring IDH1-R132 mutation will be included in Cohort 1, and patients with R/R AML harboring IDH2-R140, R172 mutations will be included in Cohort 2. The two cohorts will be designed independently, analyzed separately, and subjected to statistical hypothesis testing separately. Patients in both cohorts will be randomly assigned according to the central randomization system (IWRS) in a 1:1 ratio into the experimental group and the control group. Patients in the experimental group will receive HMPL-306 monotherapy at the following dose: 250 mg once daily (QD) (first cycle, C1) + 150 mg QD \[starting from the second cycle (C2)\]; patients in the control group will receive salvage chemotherapy (1 of 4), including 4 different treatment regimens: Two intensive regimens (EA± Mitox regimen and FLAG ± Ida regimen) and two non-intensive regimens (azacitidine and LoDAC). Prior to randomization, the investigator will pre-select a salvage chemotherapy regimen based on the patient's condition, and randomization will be stratified according to patients' response to prior first-line therapy (relapse within 6 months after allogeneic HSCT, relapse after 6 months after allogeneic HSCT, primary refractory without HSCT, relapse within 6 months after achieving CR/CRh without HSCT, or relapse after 6 months after achieving CR/CRh without HSCT) and the intensity of the pre-selected chemotherapy regimen (intensive chemotherapy or weak chemotherapy).
After the patients sign the pre-screening informed consent form (ICF), pre-screening (genetic testing) will be performed to determine IDH mutation status for subsequent enrollment cohort, and if a patient wants to know about RAS or FLT3 mutation status, local testing can be used to clarify the latest RAS or FLT3 hotspot mutation. Patients who meet the inclusion criteria of this study will be randomized to the experimental group or the control group to receive treatment in 28-day cycles until one of the following conditions occurs: Treatment failure \[refer to the Guidelines for Clinical Development of New Drugs for Acute Myeloid Leukemia issued by the Center for Drug Evaluation (CDE)\]. The definition of "treatment failure" is recommended as: Treatment failure occurs when CR or CRh/CRi is not achieved after 2 cycles of treatment per protocol using the regimens for the intensive chemotherapy group. When using the regimens for the weak chemotherapy group and the experimental group, treatment failure occurs if CR or CRh/CRi is not achieved after 4 cycles of treatment, i.e., disease progression/relapse, death, unacceptable toxicity, receiving new anti-tumor therapy, judgment by the investigator that the patient no longer obtains clinical benefit from treatment, withdrawal from the study by the patient or his/her legally acceptable representative, loss to follow-up, or end of the study occurs, whichever occurs first (The treatment duration of EA±Mitox regimen and FLAG±Ida regimen in the chemotherapy group will be adjusted according to the actual medication, and a maximum of two treatment cycles will be used).
Crossover is not allowed for patients with progressive disease in the control group and the experimental group, and patients in the control group will not be allowed to crossover to other salvage regimens.
The information on treatment groups is as follows (same for both cohorts):
The experimental group: Patients treated with HMPL-306 monotherapy:
\- The dose of HMPL-306 is 250 mg QD (C1) + 150 mg QD (starting from C2), continuous, PO, in 28-day treatment cycles.
The control group: Patients treated with one of the following regimens, and the regimen will be determined by the investigator on a case-by-case basis:
* EA±Mitox regimen: Etoposide Injection 100 mg/m2, Cytarabine Injection 100-150 mg/m2, and Mitoxantrone Injection 8 mg/m2, QD, intravenous (IV) administration for 5 consecutive days (Days 1-5). (In the case that Mitoxantrone Injection is not accessible, a regimen containing mitoxantrone liposome can be used, specifically: Mitoxantrone liposome + cytarabine + etoposide regimen: Mitoxantrone liposome 24-32 mg/m2, Day 1; Cytarabine 100-200 mg/m2, Day 1 to Day 7; and Etoposide 100 mg/m2, Days 1-5). The regimen can be used with or without mitoxantrone, which can be determined by the investigator based on the actual condition of the patient.
* FLAG±Ida regimen: G-CSF Injection 300 mcg/m2, QD subcutaneous administration for 5 consecutive days (Days 1-5); Fludarabine Injection 30 mg/m2, QD IV for 5 consecutive days (Days 2-6); Cytarabine Injection 1000-2000 mg/m2, QD IV for 5 consecutive days (Days 2-6); and Idarubicin Injection 10 mg/m2, QD IV for 3 consecutive days (Days 2-4). This regimen can be used with or without Ida, which can be determined by the investigator based on the actual condition of the patient. After the end of chemotherapy administration, the investigator will determine whether it is necessary to continue the administration of G-CSF, and if necessary, retreatment with G-CSF is allowed until absolute neutrophil count (ANC) \> 0.5x109/L.
* LoDAC: Cytarabine Injection 20 mg every 12 hours, subcutaneous or IV for 10 consecutive days (Days 1-10).
* Azacitidine: Azacitidine Injection 75 mg/m2, QD, subcutaneous or IV for 7 consecutive days (Days 1-7).
Study Period:
The study includes pre-screening period, screening period, treatment period and follow-up period \[including end of treatment (EOT) follow-up, safety observation follow-up, EFS follow-up, and OS follow-up\].
The pre-screening period is defined as the period from signing the pre-screening ICF to obtaining the IDH1 and IDH2 mutation testing reports. For patients without previous IDH1 or IDH2 testing reported, specimens should be sent to the central laboratory for IDH1 and IDH2 mutation testing and other companion gene testing after signing the pre-screening ICF and prior to screening. Patients with a previously reported positive IDH1 and/or IDH2 mutation test may proceed directly to screening without pre-screening if approved by the investigator. The results confirmed by the central laboratory are required for enrollment.
The screening period is defined as the period from signing the main screening ICF to Cycle 1 Day 1 pre-dose.
Treatment period is defined as the period from the first dose to EOT. EOT Follow-up: Patients with EOT need to return to the site for EOT follow-up within 1-7 days after discontinuing treatment, or before starting other anti-tumor therapy, whichever occurs first.
Safety Observation Follow-up: Patients with EOT need to return to the site for Safety Observation Follow-up within 30 (±7) days after the last dose of study drug treatment or before starting other anti-tumor therapy, whichever occurs first.
EFS Follow-up: Patients with EOT (except for EOT due to disease progression/relapse) will be advised to remain in the study for EFS follow-up, and patients without medication after randomization will also be advised for EFS follow-up, from the day of entering EFS follow-up, and then every 8 weeks until disease progression/relapse, death, withdrawal by the patient or his/her legally acceptable representative, patient lost to follow-up, or end of study, whichever occurs first. Subsequent new transplant conditioning regimens or new anti-tumor treatment regimens will be documented during EFS follow-up.
OS Follow-up: Patients who have been randomized and have completed EFS follow-up (and who have EOT due to disease progression/relapse) will receive OS follow-up every 8 weeks from the date they enter OS follow-up until death, withdrawal by the patient and his/her legally acceptable representative, loss to follow-up, or end of study, whichever occurs first. If a patient withdraws from treatment and not from the entire study, EFS and OS data collection will be continued.
End of Study Inconsistent time of end of study is allowed between the two cohorts. The end of study for each cohort is defined as the time when the target number of OS events for the final analysis is reached in the cohort. The actual duration of study for each cohort will depend on the actual enrollment rate, dropout rate, and the length of median OS in each group.
Efficacy Assessment(s) Efficacy evaluation will be based on modified 2022 European Leukemia Net (ELN) criteria. Efficacy assessment will be performed once for each of the first 6 cycles of study drug treatment (i.e., C2D1, C3D1, C4D1, C5D1, C6D1, C7D1) and every 2 cycles after 6 cycles of treatment (i.e., C9D1, C11D1, C13D1, ......); Efficacy assessments will also be performed at the Safety Observation Follow-up and each EFS Follow-up.
Safety Assessment(s) All adverse events (AEs) will be graded according to the National Cancer Institute Common Terminology Criteria for Adverse Events (NCI CTCAE) version 5.0. AEs will be coded using Medical Dictionary for Regulatory Activities (MedDRA). The number and incidence of treatment-emergent adverse events (TEAEs) will be summarized by system organ class and preferred term.
All the serious adverse events (SAEs) related with the study procedure will be collected from the date of the signing of informed consent form for pre-screening to the date of the signing of master informed consent form; all the SAEs will be collected from the date of the signing of master informed consent form to the date when the first dose is given; all AEs/SAEs will be collected from the date when the first dose is given to 30 days after the last dose is given, or the date when a new anti-tumor therapy is started, whichever occurs first (If HSCT is performed, safety data on and after HSCT treatment will no longer be collected; If a patient experiences disease recurrence after HSCT and is re-enrolled to receive HMPL-306 treatment, the adverse events after HSCT need to be collected); SAEs confirmed by the investigator to have a reasonable possibility of correlation with the study drug will be collected 30 days after the last dose or after the start of a new antitumor therapy, whichever occurs first.
Study Oversight
Has Oversight DMC:
True
Is a FDA Regulated Drug?:
False
Is a FDA Regulated Device?:
False
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
False
Is an FDA AA801 Violation?: