Protocol Number: HJKC3-0003. Treatment Free Remission After Asciminib Based Therapy in Chronic Phase Chronic Myeloid Leukemia (CP-CML) Patients Who Relapsed After a Prior Attempt at TKI Discontinuation

NCT ID: NCT04838041

Last Updated: 2025-07-30

Basic Information

• Recruitment Status: RECRUITING
• Clinical Phase: PHASE2
• Total Enrollment: 51 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2021-11-11
• Study Completion Date: 2029-07-31

Brief Summary

This is a single arm phase II study that will enroll a minimum of 47 subjects with a maximum of 51. All patients will have a confirmed diagnosis of chronic phase chronic myeloid Leukemia and must have previously attempted to discontinue Tyrosine Kinase inhibitors (TKI). All patients must have restarted the same TKI they were on prior to discontinuation at the time of relapse in order to be eligible for this trial.

Detailed Description

All eligible patients will begin asciminib plus/minus TKI on cycle 1 day 1 of the consolidation phase. They will continue therapy for a total of 12 cycles (minimum of 12 months). Each cycle will be ~28 days. At the end of 12 cycles, asciminib plus/minus TKI will be discontinued in patients who continue to satisfy the requirements for TFR attempt. The primary endpoint of this study is the 12-month 'second' TFR rate after completion of 12 cycles of asciminib based therapy. Patients will remain in the TFR phase of the study for up to three years and will have central PCR testing during the first two years. PCR testing will continue locally thereafter. Therefore, the total duration of the subject participation trial will be approximately five years (one year on consolidation phase + three years in the TFR phase + one year of long-term follow-up post TFR or early discontinuation.

Conditions

Chronic Phase Chronic Myelogenous Leukemia

Study Design

• Allocation Method: NON_RANDOMIZED
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Asciminib 40 mg PO daily plus imatinib (maximum dose of 400 mg PO once daily)

All eligible patients will begin asciminib plus/minus TKI on cycle 1 day 1 of the consolidation phase. They will continue therapy for a total of 12 cycles (minimum of 12 months). Each cycle will be \~28 days. At the end of 12 cycles, asciminib plus/minus TKI will be discontinued in patients who continue to satisfy the requirements for TFR attempt.

Group Type: EXPERIMENTAL

Asciminib 40 MG

Intervention Type: DRUG

40 mg by mouth (PO) when used with imatinib.

Imatinib

Intervention Type: DRUG

Maximum dose of 400 mg PO once daily.

Asciminib 40 mg twice daily plus nilotinib (maximum dose of 300 mg twice daily)

All eligible patients will begin asciminib plus/minus TKI on cycle 1 day 1 of the consolidation phase. They will continue therapy for a total of 12 cycles (minimum of 12 months). Each cycle will be \~28 days. At the end of 12 cycles, asciminib plus/minus TKI will be discontinued in patients who continue to satisfy the requirements for TFR attempt.

Group Type: EXPERIMENTAL

Asciminib 40 MG Twice Daily

Intervention Type: DRUG

40 mg twice daily when used with nilotinib.

Nilotinib

Intervention Type: DRUG

Maximum dose of 300 mg twice daily.

Asciminib 80 mg daily plus dasatinib (maximum dose of 100 mg PO once daily)

All eligible patients will begin asciminib plus/minus TKI on cycle 1 day 1 of the consolidation phase. They will continue therapy for a total of 12 cycles (minimum of 12 months). Each cycle will be \~28 days. At the end of 12 cycles, asciminib plus/minus TKI will be discontinued in patients who continue to satisfy the requirements for TFR attempt.

Group Type: EXPERIMENTAL

Asciminib 80 MG daily

Intervention Type: DRUG

80 mg daily when used with dasatinib or taken alone.

Dasatinib

Intervention Type: DRUG

Maximum dose of 100 mg PO once daily.

Asciminib 80 mg PO daily taken alone

All eligible patients will begin asciminib plus/minus TKI on cycle 1 day 1 of the consolidation phase. They will continue therapy for a total of 12 cycles (minimum of 12 months). Each cycle will be \~28 days. At the end of 12 cycles, asciminib plus/minus TKI will be discontinued in patients who continue to satisfy the requirements for TFR attempt.

Group Type: EXPERIMENTAL

Asciminib 80 MG daily

Intervention Type: DRUG

80 mg daily when used with dasatinib or taken alone.

Interventions

Asciminib 40 MG

40 mg by mouth (PO) when used with imatinib.

Intervention Type: DRUG

Asciminib 40 MG Twice Daily

40 mg twice daily when used with nilotinib.

Intervention Type: DRUG

Asciminib 80 MG daily

80 mg daily when used with dasatinib or taken alone.

Intervention Type: DRUG

Imatinib

Maximum dose of 400 mg PO once daily.

Intervention Type: DRUG

Nilotinib

Maximum dose of 300 mg twice daily.

Intervention Type: DRUG

Dasatinib

Maximum dose of 100 mg PO once daily.

Intervention Type: DRUG

Other Intervention Names

ABL001; ABL001; ABL001; Gleevec; TASIGNA; Sprycel

Eligibility Criteria

Inclusion Criteria

1. Age ≥18 years old.

2. Willing and able to give informed consent.

3. Diagnosed with chronic myelogenous leukemia (CML) in chronic phase without BCR::ABL1 ^T315I and have either the b3a2 (e14a2) or b2a2 (e13a2) variants that give rise to the p210 BCR::ABL1 protein. Subtype classification whether b3a2 (e14a2) or b2a2 (e13a2) is not required for study eligibility.

4. Must have a documented history of attempting only one prior TKI discontinuation under the guidance of a treating physician. TKI includes dasatinib, imatinib or nilotinib.

5. Must have met all the following criteria prior to first attempt to discontinue their TKI:

• Stable molecular response (MR4; < 0.01% IS) for > 2 years (with allowance for a two-week variance), as documented on at least four tests, performed at least three months apart (e.g., If a patient has had >4 PCR tests performed during the two years leading up to their initial TKI discontinuation, any value between 0.01 and 0.05% IS is considered a stable result, however, at least four tests must be < 0.01% IS. If any results are >0.05% IS, tests must have been repeated within one month and be less than 0.01% IS and stable.
• Treatment with one of the following FDA approved TKIs; imatinib, dasatinib, nilotinib at any dose for a minimum of approximately three years (allowance of a four-week variance) prior to discontinuing TKIs.
• Has been on any number of TKIs, but has not been resistant to any TKI (changes made for intolerance are allowed).

6. Must have relapsed (defined as loss of major molecular response (MMR), RQ-PCR for BCR::ABL1 >0.1% IS after first attempted TKI discontinuation.

7. After first failed TFR attempt, must have a minimum duration of one year of retreatment with TKI, and must plan to remain on that TKI or switch to asciminib for a minimum of 12 months during the consolidation treatment phase.

8. Current TKI must be the same as the TKI being taken prior to the initial TFR attempt (e.g., if patient is on imatinib prior to first TFR attempt, they should be on imatinib at time of enrollment on this study).

9. Eastern Cooperative Oncology Group (ECOG) performance status 0-3.

10. Must have a RQ-PCR for BCR::ABL1 < 0.0032% IS (MR4.5) reported by the trial designated central lab at the time of study enrollment.

11. Lipase ≤ 1.5 x upper limit of normal (ULN). For lipase > ULN - ≤ 1.5 x ULN, value should be considered not clinically significant and not associated with risk factors for acute pancreatitis.

12. eGFR ≥ 30 mL/min as calculated using the 2021 chronic kidney disease epidemiology (CKD-EPI) creatinine equation (https://www.kidney.org/professionals/kdoqi/gfr_calculator)

13. Female patients must meet one of the following:

• Postmenopausal for at least one year before the screening visit,
• Surgically sterile
• If they are of childbearing potential, agree to practice two effective methods of contraception from the time of signing of the informed consent form through 90 days after the last dose of study drug,
• Must also adhere to the guidelines of any treatment-specific pregnancy prevention program, if applicable
• Agree to practice true abstinence when this is in line with the preferred and usual lifestyle of the subject. (Periodic abstinence [e.g., calendar, ovulation, symptothermal, postovulation methods] and withdrawal are not acceptable contraception methods.)

14. Male patients, even if surgically sterilized (i.e., status post vasectomy), must agree to one of the following:

• Practice effective barrier contraception during the entire study treatment period and through 90 days after the last study drug dose.
• Must also adhere to the guidelines of any treatment-specific pregnancy prevention program, if applicable.
• Agree to practice true abstinence when this is in line with the preferred and usual lifestyle of the subject. (Periodic abstinence [e.g., calendar, ovulation, symptothermal, postovulation methods] and withdrawal are not acceptable methods of contraception.)

Exclusion Criteria

1. History of accelerated or blast phase CML.

2. A second malignancy requiring active treatment.

3. History of recent (within 12 months) acute pancreatitis or chronic pancreatitis.

4. Subjects who have previously received treatment with asciminib.

5. Subjects with platelet (PLT) count < 100 × 109/L or an absolute neutrophil count (ANC) of < 1 × 109/L or hemoglobin < 8 g/dL.

6. Aspartate aminotransferase (AST) and alanine transaminase (ALT) ≥3 times the institutional upper limit of normal.

7. Total bilirubin ≥ 1.5 times the institutional upper limit of normal (unless direct bilirubin is within normal limits).

8. Pregnant or lactating.

9. Unable to comply with lab appointment schedule and patient-reported outcome (PRO) assessments.

10. Another investigational drug within four weeks of enrollment.

11. Any serious medical or psychiatric illness that could, in the investigator's opinion, interfere with the completion of treatment according to this protocol.

12. Patient has undergone a prior allogeneic stem cell transplant.

13. Screening 12-lead electrocardiogram (ECG) showing a baseline corrected QT interval >480msec (patients with a pacemaker will still be eligible with QTc>500msec).

14. Known active hepatitis B infection.

Eligibility for TFR Phase:

1. Stable molecular response (MR4.5; < 0.0032% IS) documented on at least three tests (may include TFR phase screening PCR) by the trial designated lab, performed approximately three months apart while on consolidation phase.

2. TFR phase screening PCR RQ-PCR for BCR::ABL1 < 0.0032% IS (MR4.5) by the trial designated lab.

3. ECOG 0-3.

4. Completion of 12 cycles on the consolidation therapy phase.

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

H. Jean Khoury Cure CML Consortium

OTHER

Sponsor Role: collaborator

Medical College of Wisconsin

OTHER

Sponsor Role: lead

Responsible Party

Ehab L Atallah

Professor

Responsibility Role: PRINCIPAL_INVESTIGATOR

Principal Investigators

Ehab Atallah, MD

Role: PRINCIPAL_INVESTIGATOR

Medical College of Wisconsin

Michael J. Mauro, MD

Role: STUDY_CHAIR

Memorial Sloan Kettering Cancer Center

Locations

The Barbara Ann Karmanos Cancer Institute

Detroit, Michigan, United States

Site Status: RECRUITING

Memorial Sloan Kettering Cancer Center

New York, New York, United States

Site Status: RECRUITING

Huntsman Cancer Institute

Salt Lake City, Utah, United States

Site Status: RECRUITING

Froedtert Hospital & the Medical College of Wisconsin

Milwaukee, Wisconsin, United States

Site Status: RECRUITING

Countries

United States

Central Contacts

Medical College of Wisconsin Cancer Center Clinical Trials Office

Role: CONTACT

cccto@mcw.edu

414-805-8900

Ehab Atallah, MD

Role: CONTACT

eatallah@mcw.edu

414-805-4600

Facility Contacts

Sharon Prokop

Role: primary

prokops@karmanos.org

313-576-9363

Michael Mauro, MD

Role: primary

maurom@mskcc.org

Srinivas Tantravahi, MBBS

Role: primary

Srinivas.Tantravahi@hci.utah.edu

Ehab Atallah, MD

Role: primary

eatallah@mcw.edu

414-805-4600

Other Identifiers

PRO00040685

Identifier Type: -

Identifier Source: org_study_id