Study of HQP1351 in Subjects With Refractory CML and Ph+ ALL
A multi-center, open-label, randomized, phase Ib study to evaluate the pharmacokinetics (PK) of HQP1351 and to determine the recommended phase 2 dose (RP2D) of HQP1351 in subjects with CML chronic phase (CP), accelerated phase (AP) or blast phase (BP) or with Ph+ ALL, who have experienced resistance or intolerance to at least three tyrosine kinase inhibitors (TKIs).
- Leukemia, Myeloid, Chronic
- Myeloid Leukemia
- Chronic Myeloid Leukemia
- Philadelphia Positive Acute Lymphoblastic Leukemia
- Eligible Ages
- Over 18 Years
- Eligible Genders
- Accepts Healthy Volunteers
- Patients must have CML in any phase (CP, AP, or BP of any phenotype) or Ph+ ALL, with or without T315I mutation - Be previously treated with and developed resistance or intolerance to at least three TKIs including ponatinib, imatinib, dasatinib, nilotinib, and bosutinib). For patients with a T315I mutation, resistance or intolerance to ponatinib alone is acceptable. 1. The definition of resistance to first-line TKI treatment refers to European Leukemia Net (ELN) recommendations. The definitions are the same for patients in CP, AP, BP and Ph+ ALL, and apply also to second-line treatment, when first-line treatment was changed for intolerance. The patients must meet at least one criterion. 1. Three months after the initiation of therapy: non-complete hematologic response (CHR) and/or Ph+ >95% 2. Six months after the initiation of therapy: BCR-ABL1>10% and/or Ph+ >35% 3. Twelve months after the initiation of therapy: BCR-ABL1>1% and/or Ph+ >0% 4. Then, and at any time after the initiation of therapy: Loss of CHR, or loss of complete cytogenetic response (CCyR), or confirmed loss of major molecular response (MMR) (In 2 consecutive tests, of which one with a BCR-ABL1 transcripts level≥1%), mutations, clonal chromosome abnormalities in Ph+ cells (CCA/Ph+) 2. The definition of resistance to second-line TKI treatment a) For CML CP patients: the patients must meet at least one criterion as follows: i.) Three months after the initiation of therapy: No CHR or Ph+ >95% or new mutations ii.) Six months after the initiation of therapy: BCR-ABL1>10% and/or Ph+ >65% and/or new mutations iii.) Twelve months after the initiation of therapy: BCR-ABL1>10% and/or Ph+ >35% and/or new mutations iv.) Then, and at any time after the initiation of therapy: Loss of CHR or loss of CCyR, new mutations, confirmed loss of MMR (In 2 consecutive tests, of which one with a BCR-ABL1 transcripts level≥1%), clonal chromosome abnormalities in Ph+ cells (CCA/Ph+) b) For CML AP patients: the patients must meet at least one criterion as follows: i.) Three months after the initiation of therapy: failure to achieve a major hematologic response (MaHR) ii.) At any time after the initiation of therapy, the loss of a MaHR, confirmed in at least 2 consecutive analyses separated by at least 4 weeks iii.) At any time after the initiation of therapy, the development of new BCR-ABL kinase domain mutations in the absence of a MaHR c) For CML BP and Ph+ ALL patients: the patients must meet at least one criterion as follows: i) One month after the initiation of therapy: failure to achieve a MaHR ii) At any time after the initiation of therapy, the loss of a MaHR, confirmed in at least 2 consecutive analyses separated by at least 1week iii) At any time after the initiation of therapy, the development of new BCR-ABL kinase domain mutations in the absence of a MaHR 3. Intolerance to TKIs is defined as: 1. Non-hematological AEs: patients with grade 3 or 4 toxicity during TKIs treatment, or with persistent grade 2 toxicity, unresponsive to optimal management, including dose adjustments in the absence of a CCyR for CP patients or MaHR for AP/BP or Ph+ ALL patients 2. Hematological AEs: patients with grade 3 or 4 toxicity during TKIs treatment, that is recurrent after unresponsive after optimal management, including dose adjustments in the absence of a CCyR for CP patients or MaHR for AP/BP or Ph+ ALL patients - Patients providing written informed consent before initiation of any study-related activities - Eastern Cooperative Oncology Group (ECOG) performance status ≤2 - Minimum life expectancy of 3 months or more - Patients with adequate organ function as defined below: 1. Creatinine < 2 × upper limit of normal (ULN); or, creatinine > 2 × ULN, with 24h glomerular filtration rate (GFR) ≥ 30 mL/min (Cockcroft-Gault) 2. Serum albumin ≥ 3.0 g/dL 3. Total bilirubin < 1.5 × ULN 4. Aspartate aminotransferase (AST [Serum glutamic oxaloacetic transaminase (SGOT)]) and alanine aminotransferase (ALT [serum glutamate-pyruvate transaminase (SGPT)]) < 3 × ULN for institution (<5×ULN if liver involvement with leukemia) 5. Serum amylase and lipase ≤ 1.5 × ULN 6. Prothrombin time (PT) ≤ 1.5 × ULN - Heart function: Left ventricular ejection fraction (LVEF) > 50% - Normal QT interval corrected Fridericia (QTcF) interval on screening electrocardiogram (ECG) evaluation: male ≤450ms, female ≤470ms - For females of childbearing potential, a negative pregnancy test must be established before enrollment. And the eligible female and male patients with childbearing potential must agree to use an effective form of contraception with their sexual partners throughout participation in this study - Ability to comply with study procedures, in the Investigator's opinion
- Received TKI therapy within 5 half-lives or 7 days prior to first dose of HQP1351, whichever is shorter, or any adverse events (AEs) (except alopecia and pigmentation) not recovered to CTCAE v5.0 grade 0-1 due to any other treatments - Received other therapies as follows: 1. For CP and AP patients, received hydroxyurea or anagrelide within 24 hours prior to the first dose of HQP1351; or, interferon, immunotherapy or cytarabine within 14 days prior to the first dose of HQP1351; or, any other radiotherapy, cytotoxic chemotherapy or investigational therapy within 28 days prior to receiving the first dose of HQP1351 2. For BP patients, received chemotherapy within 7 days prior to the first dose of HQP1351 3. For Ph+ ALL patients, received corticosteroids within 24 hours before the first dose of HQP1351, or received chemotherapy within 7 days prior to the first dose of HQP1351 4. Patients who are currently receiving treatment with a medication that has the potential to interact with HQP1351 5. Patients who had been treated with HQP1351 6. Patients requiring immunosuppressive therapy other than short time of steroid - Impairment of gastrointestinal (GI) function or GI disease that may significantly alter absorption of study drugs - Patients with cardiovascular diseases, including uncontrolled high blood pressure (HBP) (that is blood pressure >140/90mmHg.); or, receiving drugs that can cause prolonged QT interval. The patients with well controlled HBP can be considered to be included. (the "well controlled HBP" is defined as: HBP can be ≤ 140/90mmHg with antihypertensive treatment). Those requiring 3 or more antihypertensive medications should be discussed with the medical monitor. - Have clinically significant, uncontrolled, or active cardiovascular disease, specifically including, but not restricted to: 1. Any history of myocardial infarction (MI) within 6 months or unstable angina within 3 months 2. Any history of cerebrovascular accident within 1 year, or transient ischemic attack (TIA) within 3 months 3. Any history of peripheral vascular infarction, including visceral infarction within 6 months 4. Congestive heart failure (CHF) (New York Heart Association [NYHA] class III or IV) within 6 months prior to enrollment, or left ventricular ejection fraction (LVEF) less than lower limit of normal, per local institutional standards, within 6 months prior to enrollment 5. History of clinically significant (as determined by the treating physician) atrial arrhythmia or any history of ventricular arrhythmia 6. Venous thromboembolism, including deep venous thrombosis or pulmonary embolism, within 3 months prior to enrollment. Patients who have experienced a venous thromboembolic event should only be eligible if the condition is well controlled with optimal intervention (as determined by the treating physician). Continued prophylactic anticoagulation is acceptable. 7. Patients with revascularization procedures including cardiac bypass within the 6 months and stenting within the past 3 months should be excluded. - Have history of autologous or allogeneic stem cell transplant, or with active graft-versus-host disease (GVHD), or active immune suppression in recent 6 months prior to informed consent date or active immune suppression in recent 6 months prior to informed consent date - CML CP patients with CCyR - Patients who have a significant bleeding disorder unrelated to CML or Ph+ ALL - Patients who had a major surgery within 4 weeks prior to study entry or have not recovered from side effects of such surgery which the Investigator considers not appropriate for enrollment - Cytologically confirmed central nervous system (CNS) involvement (if asymptomatic, spinal fluid examination is not necessary prior to first treatment) - Patients with another primary malignancy within 1 years of study entry. Patients with nonmelanoma skin cancer or carcinoma in situ of any type are not excluded if they have undergone complete resection and are considered disease-free at the time of study entry. - Have ongoing or active infection, including known history of immunodeficiency virus (HIV) or HIV antibody positive, hepatitis B virus (HBV) or HBsAg positive, hepatitis C virus (HCV). Patients who have positive HCV antibody must have an undetectable HCV viral load. - Patients who have poorly controlled diabetes, defined as HbA1C values of > 7.5%. Patients with pre-existing, well-controlled diabetes are not excluded. - Known allergy to any components in the study drug - Pregnant or lactating - Patients who have any conditions or illness that, according to the opinions of the investigator or the medical monitor, would comprise patient safety or interfere with the evaluation of safety and efficacy to the study drug
- Phase 1
- Study Type
- Intervention Model
- Parallel Assignment
- Intervention Model Description
- A total of 30 patients will be randomized at 1:1:1 ratio into one of the three dose cohorts: 30 mg every other day (QOD), 40 mg QOD and 50 mg QOD, with 10 patients per dose cohort.
- Primary Purpose
- None (Open Label)
- Ascentage Pharma Group Inc.
Study ContactKathryn Shantz
A total of 30 patients will be randomized at 1:1:1 ratio into one of the three dose cohorts: 30 mg every other day (QOD), 40 mg QOD, and 50 mg QOD, with 10 patients per dose cohort. The first cycle of 28 days is considered as the dose-limiting toxicity (DLT) observation period. If the incidence of DLTs exceeds 20% (2 patients) in 50 mg dose cohort during the first cycle of therapy, this dose cohort will be stopped. The randomization will be stratified to 4 groups: T315I mutated CML-CP and CML-AP, T315I un-mutated CML-CP, T315I unmutated CML-AP, and CML-BP and Ph+ ALL to ensure that the subgroups are represented across all dose cohorts. Blood samples will be collected from each subject at specified time points to evaluate the PK of HQP1351. RP2D of HQP1351 will be determined based on the comprehensive analyses of the PK, safety, and efficacy data of the US patients treated with HQP1351, when compared with that in the Chinese patients. Eligible patients will have disease resistance to or intolerance to at least three TKIs, for patients with T315I mutation, resistance or intolerance to ponatinib alone is acceptable. Patients will be administered HQP1351 orally every other day (QOD) during a period of 28 days (1 cycle).