Venetoclax After TKI to Target Persisting Stem Cells in CML

NCT ID: NCT05701215

Last Updated: 2025-03-10

Basic Information

• Recruitment Status: ACTIVE_NOT_RECRUITING
• Clinical Phase: PHASE2
• Total Enrollment: 10 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2023-08-31
• Study Completion Date: 2026-01-31

Brief Summary

There is currently no available treatment, capable to increase the rate of sustained deep molecular remissions after TKI discontinuation in CML. Venetoclax could be such a drug. The study will provide unprecedented biological insights on the effects of venetoclax in controlling minimal residual stem cell disease induced by long-term prior TKI therapy. If the study would be positive, the findings could become practice changing for patients in deep molecular remission under TKI and willing to tolerate a temporary additional treatment.

Conditions

Chronic Myeloid Leukemia

Study Design

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

Study Groups

Venetoclax

Venetoclax will be taken orally once daily (400 mg) for 12 months after stop of TKI

Group Type: EXPERIMENTAL

Venetoclax

Intervention Type: DRUG

Venetoclax will be taken orally once daily (400 mg) for 12 months

Interventions

Venetoclax

Venetoclax will be taken orally once daily (400 mg) for 12 months

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

1. Patients with diagnosis of chronic phase CML with cytogenetic confirmation of the Philadelphia (Ph) chromosome

2. Ph negative cases or patients with variant translocations who are BCR::ABL1 positive in multiplex PCR are also eligible

3. Typical b2a2 and/or b3a2 BCR::ABL1 transcripts

4. Subject must be ≥ 18 years of age

5. Stored DNA from initial diagnosis (prior TKI treatment) for BCR::ABL1 breakpoint analysis

6. BCR::ABL1 transcript level according to the international scale (IS) of MR4 or better which has been confirmed three times within the past 13 months and was assessed by an IS-certified reference laboratory, such as of the University Jena or another MR4-certified laboratory in Germany

7. At least 3 years of TKI therapy

8. Patients who failed to discontinue TKI in a prior discontinuation attempt are still eligible if they fulfill criteria 6 after retreatment with TKI

9. WHO performance status 0-2

10. Adequate end organ function as defined by:

• Total bilirubin (TBL) < 3 x Upper Limit of Normal (ULN); patients with Gilbert's syndrome may only be included if TBL ≤ 3.0 x ULN or direct bilirubin ≤ 1.5 x ULN,
• Creatinine Clearance (CrCl) ≥ 30 millilitres per minute (mL/min) as calculated using Cockcroft-Gault formula, Serum lipase ≤ 1.5 x ULN. For serum lipase > ULN 1.5 x ULN, value must be considered not clinically significant and not associated with risk factors for acute pancreatitis.

11. Patients must have the following laboratory values within normal limits or corrected to within normal limits with supplements:

• Potassium (potassium increase of up to 6.0 mmol/L is acceptable if associated with CrCl ≥ 90 mL/min),
• Total calcium (corrected for serum albumin); (calcium increase of up to 12.5 mg/dl or 3.1 mmol/L is acceptable if associated with CrCl ≥ 90 mL/min),
• Magnesium (magnesium increase of up to 3.0 mg/dL or 1.23 mmol/L if associated with CrCl ≥ 90 mL/min),
• For patients with mild to moderate renal impairment (CrCl ≥ 30 mL/min and <90 mL/min) - potassium, total calcium (corrected for serum albumin) and magnesium should be within normal limits or corrected to within normal limits with supplements.

12. Women of childbearing age must use a highly effective method of contraception while using venetoclax. Women using hormonal contraceptives should also use a barrier method.

13. Negative pregnancy test in women of childbearing potential

14. Subject must voluntarily sign and date an informed consent

Exclusion Criteria

1. Concomitant use of strong CYP3A-Inhibtors (e.g., itraconazole, ketoconazole, posaconazole, voriconazole, clarithromycin, ritonavir) is contraindicated

2. Concomitant use of moderate CYP3A-Inhibitors (e.g., ciprofloxacin, diltiazem, erythromycin, fluconazole, verapamil) should be avoided.

3. Grapefruit products, Seville oranges, and starfruit (carambola) should be avoided during treatment with venetoclax as they contain inhibitors of CYP3A

4. Concomitant use of venetoclax with P-gp and BCRP inhibitors

5. Concomitant use of venetoclax with strong CYP3A inducers (e.g., carbamazepine, phenytoin, rifampin) or moderate CYP3A inducers (e.g., bosentan, efavirenz, etravirine, modafinil, nafcillin) should be avoided

6. Concomitant use of preparations containing St. John´s wort

7. Patients with severe renal impairment (Crea-Clearance < 30 ml/min) or on dialysis

8. Patients with severe hepatic impairment

9. Patients who are pregnant or breast feeding, or females of reproductive potential not employing an effective method of birth control. Female patients must agree to employ an effective barrier method of birth control throughout the study and for and for at least 30 days after ending venetoclax treatment

10. Known impaired cardiac function

11. Impaired gastrointestinal function or disease that may alter the absorption of study drug

12. Patients who have undergone major surgery ≤ 2 weeks prior to starting study drug or who have not recovered from side effects of such therapy

13. Active or uncontrolled infections at the time of enrolment

14. Known HIV sero-positivity or known active hepatitis B or C infection (HIV testing is not required)

15. Participation in another clinical study with other investigational drugs within 14 days prior to enrolment

16. Any medical, mental, psychological or psychiatric condition that in the opinion of the investigator would not permit the patient to complete the study or understand the patient information

17. Subject has acute leukemia

18. Subject has known active CNS involvement.

19. Hypersensitivity to venetoclax or any component of the formulation

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

Sponsors

Ludwig-Maximilians - University of Munich

OTHER

Sponsor Role: collaborator

AbbVie

INDUSTRY

Sponsor Role: collaborator

Thomas Ernst, PD Dr. med.

OTHER

Sponsor Role: lead

Responsible Party

Thomas Ernst, PD Dr. med.

Principal Investigator

Responsibility Role: SPONSOR_INVESTIGATOR

Principal Investigators

Thomas Ernst, Prof. Dr.

Role: PRINCIPAL_INVESTIGATOR

University Hospital Jena

Locations

Uniklinik der RWTH Aachen

Aachen, , Germany

Universitätsklinikum Jena

Jena, , Germany

Countries

Germany

Other Identifiers

2022-003069-39

Identifier Type: EUDRACT_NUMBER

Identifier Source: secondary_id

VARIANT

Identifier Type: -

Identifier Source: org_study_id