Clinical Trials List
Protocol NumberM26-092
NCT Number(ClinicalTrials.gov Identfier)NCT07581002
Active
2026-06-01 - 2032-11-30
Phase II/III
Not yet recruiting5
A Randomized Phase 2/3 Study Evaluating the Safety and Efficacy of Pivekimab Sunirine (PVEK) in Combination with Venetoclax and Azacitidine in Adult Subjects with Newly Diagnosed Acute Myeloid Leukemia (AML) Ineligible to Receive Intensive Chemotherapy
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Trial Applicant
AbbVie
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Sponsor
ABBVIE BIOPHARMACEUTICALS GMBH TAIWAN BRANCH (SWITZERLAND)
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Trial scale
Multi-Regional Multi-Center
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Update
2026/09/15
Investigators and Locations
Co-Principal Investigator
- Wen-Chien Chou 無
- MING YAO 無
- Shang-Ju Wu 無
- Huai-Hsuan Huang 無
- Chien-Chin Lin 無
- Chieh-Lung Cheng 無
- CHENG-HONG TSAI 無
- - - 無
- 田豐銘 無
- 林明恩 無
- YAO CHI-YUAN 無
- 李思慧 無
- 楊鎰聰 無
- 李婉瑄 無
The Actual Total Number of Participants Enrolled
0 Not yet recruiting
Co-Principal Investigator
- Tzu-Ting Chen 無
- Che-Hung Lin 無
- Ming-Yu Lien 無
- Chi-Ching Chen 無
- Ching-Chan Lin 無
- 鄭富銘 無
- 陳珈妤 無
- 王幸婷 無
The Actual Total Number of Participants Enrolled
0 Not yet recruiting
Co-Principal Investigator
The Actual Total Number of Participants Enrolled
0 Not yet recruiting
Co-Principal Investigator
- CHENG-HSIEN LIN 無
- 滕傑林 無
- PO-WEI LIAO 無
- PO-HSIEN LI 無
- 鄧齡喬 無
The Actual Total Number of Participants Enrolled
0 Not yet recruiting
Principal Investigator
Hsiao-Wen Kao
Co-Principal Investigator
The Actual Total Number of Participants Enrolled
0 Not yet recruiting
Condition/Disease
Acute Myeloid Leukemia
Objectives
Cancer is a condition where cells in a specific part of the body grow and reproduce uncontrollably. Acute myeloid leukemia (AML) is a cancer of the blood and bone marrow (the spongy tissue inside the bones) that affects white blood cells that helps to fight infections and also prevents normal blood cell production. This study will assess the adverse events and changes in the disease activity when Pivekimab Sunirine (PVEK) is given in combination with Venetoclax (VEN) and Azacitidene (AZA) in adult participants with AML ineligible to receive intensive chemotherapy.
Pivekimab sunirine is a drug being evaluated in the treatment of AML.This is a Phase 2/Phase 3, study of PVEK. Phase 2 is open-label and randomized. Phase 3 is double-blind, randomized. Phase 2 and Phase 3 studies test potential new treatments in patients with a condition or disease. Open-label means that both patients and study doctors know which study treatment is given to patients in Phase 2 of the study. Double-blind means that neither the patients nor the study doctors know who is given which study treatment in Phase 3 of the study. Approximately 660 adult participants will be enrolled in 180 sites worldwide.
In Phase 2 of the study, patients will be randomized to receive PVEK + VEN + AZA or standard of care treatment with VEN + AZA. In Phase 3, patients will be randomized to receive PVEK + VEN + AZA or a matching-placebo for PVEK plus VEN + AZA. PVEK is given as an infusion into the vein, AZA is given as an injection under your skin (subcutaneous) or as an infusion into the vein (intravenous) (depending on country where patient enrolls), and VEN is a tablet given by mouth. The total study duration is approximately 71 months.
There may be higher treatment burden for participants in this trial compared to their standard of care. Participants will attend regular visits during the study at a hospital or clinic. The effect of the treatment will be checked by medical assessments, blood tests, and checking for side effects.
Test Drug
Azacitidine
Pivekimab sunirine (IMGN632)
Venetoclax
Venetoclax
Venetoclax
Pivekimab sunirine (IMGN632)
Venetoclax
Venetoclax
Venetoclax
Active Ingredient
Azacitidine
Pivekimab sunirine (IMGN632)
Venetoclax
Venetoclax
Venetoclax
Pivekimab sunirine (IMGN632)
Venetoclax
Venetoclax
Venetoclax
Dosage Form
N/A
Dosage
N/A
Endpoints
Phase 2: Complete remission (CR) CR per modified 2022 European LeukemiaNet (ELN) response criteria in AML Up to Approximately 71 Months
Phase 3: Complete remission (CR) CR per modified 2022 European LeukemiaNet (ELN) response criteria in AML Up to Approximately 71 Months
Phase 3: Overall Survival (OS) The time (in number of days) from randomization to death due to any cause. Up to Approximately 71 Months
Number of Participants with Adverse Events (AEs) An AE is defined as any untoward medical occurrence in a patient or clinical investigation in which a participant is administered a pharmaceutical product which does not necessarily have a causal relationship with this treatment. Up to approximately 71 months
Phase 3: Complete remission (CR) CR per modified 2022 European LeukemiaNet (ELN) response criteria in AML Up to Approximately 71 Months
Phase 3: Overall Survival (OS) The time (in number of days) from randomization to death due to any cause. Up to Approximately 71 Months
Number of Participants with Adverse Events (AEs) An AE is defined as any untoward medical occurrence in a patient or clinical investigation in which a participant is administered a pharmaceutical product which does not necessarily have a causal relationship with this treatment. Up to approximately 71 months
Inclution Criteria
Participants must have newly diagnosed, untreated confirmed acute myeloid leukemia (AML) diagnosis as per the 5th edition of World Health Organization (WHO) criteria with a projected life expectancy of at least 12 weeks.
CD123-positive
Ineligible for intensive induction therapy (chemotherapy) defined by:
≥ 75 years of age OR
≥ 18 to 74 years of age with at least one of the following co-morbidities:
Eastern Cooperative Oncology Group (ECOG) performance status of 2 or 3
Cardiac history of congestive heart failure requiring treatment or ejection fraction ≤ 50% or chronic stable angina
Diffusion capacity of the lung for carbon monoxide (DLCO) ≤ 65% or forced expiratory volume in 1 second (FEV1) ≤ 65%
Creatinine clearance ≥ 30 mL/min to < 45 mL/min
Moderate hepatic impairment with total bilirubin > 1.5 to ≤ 3.0 × upper limit of normal (ULN)
Any other comorbidity that the physician judges to be incompatible with intensive chemotherapy must be reviewed and approved by the medical monitor before study enrollment.
ECOG performance status 0 to 2 for subjects ≥ 75 years of age or 0 to 3 for subjects ≥ 18 to 74 years of age.
White blood cell (WBC) count < 25 × 10^9/L (hydroxyurea is permitted prior to beginning study treatment to reduce the WBC count to < 25 × 10^9/L).
Subjects must have adequate organ function:
Adequate renal function as demonstrated by a creatinine clearance ≥ 30 mL/min; calculated by the Cockcroft Gault formula or measured by 24-hour urine collection.
Adequate liver function as demonstrated by:
Aspartate aminotransferase (AST) ≤ 3.0 × ULN*,
Alanine aminotransferase (ALT) ≤ 3.0 × ULN*,
---*Unless considered due to leukemic organ involvement
Subjects < 75 years of age may have total bilirubin ≤ 3 x ULN
Subjects ≥ 75 years of age total bilirubin ≤ 1.5 × ULN unless elevated level is considered to be due to Gilbert's syndrome or hemolysis, total bilirubin must be < 3 x ULN and direct bilirubin < 1 x ULN
Activated partial thromboplastin time (aPTT) and prothrombin time (PT) not to exceed 1.5 × ULN International Normalized Ratio (INR) <1.5
CD123-positive
Ineligible for intensive induction therapy (chemotherapy) defined by:
≥ 75 years of age OR
≥ 18 to 74 years of age with at least one of the following co-morbidities:
Eastern Cooperative Oncology Group (ECOG) performance status of 2 or 3
Cardiac history of congestive heart failure requiring treatment or ejection fraction ≤ 50% or chronic stable angina
Diffusion capacity of the lung for carbon monoxide (DLCO) ≤ 65% or forced expiratory volume in 1 second (FEV1) ≤ 65%
Creatinine clearance ≥ 30 mL/min to < 45 mL/min
Moderate hepatic impairment with total bilirubin > 1.5 to ≤ 3.0 × upper limit of normal (ULN)
Any other comorbidity that the physician judges to be incompatible with intensive chemotherapy must be reviewed and approved by the medical monitor before study enrollment.
ECOG performance status 0 to 2 for subjects ≥ 75 years of age or 0 to 3 for subjects ≥ 18 to 74 years of age.
White blood cell (WBC) count < 25 × 10^9/L (hydroxyurea is permitted prior to beginning study treatment to reduce the WBC count to < 25 × 10^9/L).
Subjects must have adequate organ function:
Adequate renal function as demonstrated by a creatinine clearance ≥ 30 mL/min; calculated by the Cockcroft Gault formula or measured by 24-hour urine collection.
Adequate liver function as demonstrated by:
Aspartate aminotransferase (AST) ≤ 3.0 × ULN*,
Alanine aminotransferase (ALT) ≤ 3.0 × ULN*,
---*Unless considered due to leukemic organ involvement
Subjects < 75 years of age may have total bilirubin ≤ 3 x ULN
Subjects ≥ 75 years of age total bilirubin ≤ 1.5 × ULN unless elevated level is considered to be due to Gilbert's syndrome or hemolysis, total bilirubin must be < 3 x ULN and direct bilirubin < 1 x ULN
Activated partial thromboplastin time (aPTT) and prothrombin time (PT) not to exceed 1.5 × ULN International Normalized Ratio (INR) <1.5
Exclusion Criteria
Acute promyelocytic leukemia (APL), blast phase of CML or AML with t(9;22) or BCR:ABL1 fusion, transformation from myeloproliferative neoplasm (MPN), Chronic Myelomonocytic Leukemia (CMML), myelodysplastic/myeloproliferative neoplasm unspecified, or myeloid sarcoma.
Known active central nervous system (CNS) involvement with AML. Participants may have non-CNS extramedullary disease (excludes participants with myeloid sarcoma as the only disease manifestation at screening).
Participants with history of any malignancies within 2 years prior to screening with exception of: adequately treated in situ carcinoma of the cervix uteri or carcinoma in situ of the breast, in situ - carcinomas of bladder and esophagus; basal cell carcinoma of the skin or localized squamous cell carcinoma of the skin, and previous malignancy confined and surgically resected (or treated with other modalities) with curative intent and have no evidence of relapse within 2 years.
Participants must not have received a hypomethylating agent, any BCL-2 inhibitors including venetoclax, and/or chemotherapeutic agent for Myelodysplastic syndromes (MDS) or AML, CAR-T cell therapy, be currently participating in another clinical study, received any investigational treatment within 30 days prior to the first use of study combination product.
Female participant must not be pregnant or breastfeeding and is not considering becoming pregnant or donating eggs during the study and for approximately 7 months after the last dose of any study drug. Female participant of childbearing potential must agree to use at least 1 protocol specified method of birth control and male participant, if sexually active with female partner(s) of childbearing potential, must agree to practice the protocol-specified contraception.
Known active central nervous system (CNS) involvement with AML. Participants may have non-CNS extramedullary disease (excludes participants with myeloid sarcoma as the only disease manifestation at screening).
Participants with history of any malignancies within 2 years prior to screening with exception of: adequately treated in situ carcinoma of the cervix uteri or carcinoma in situ of the breast, in situ - carcinomas of bladder and esophagus; basal cell carcinoma of the skin or localized squamous cell carcinoma of the skin, and previous malignancy confined and surgically resected (or treated with other modalities) with curative intent and have no evidence of relapse within 2 years.
Participants must not have received a hypomethylating agent, any BCL-2 inhibitors including venetoclax, and/or chemotherapeutic agent for Myelodysplastic syndromes (MDS) or AML, CAR-T cell therapy, be currently participating in another clinical study, received any investigational treatment within 30 days prior to the first use of study combination product.
Female participant must not be pregnant or breastfeeding and is not considering becoming pregnant or donating eggs during the study and for approximately 7 months after the last dose of any study drug. Female participant of childbearing potential must agree to use at least 1 protocol specified method of birth control and male participant, if sexually active with female partner(s) of childbearing potential, must agree to practice the protocol-specified contraception.
The Estimated Number of Participants
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Taiwan
35 participants
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Global
660 participants
