Benefit of Venetoclax Addition (Benefit VA) in Chronic Lymphocytic Leukemia/Small Lymphocytic Lymphoma (CLL/SLL)

Status: Recruiting
Location: See all (4) locations...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Phase 2
SUMMARY

People who have chronic lymphocytic leukemia (CLL) or small lymphocytic lymphoma (SLL) are often treated with ibrutinib, acalabrutinib, or zanubrutinib. These are pills that are taken by mouth. This type of pill is called Bruton Tyrosine Kinase Inhibitor or BTKi. Another treatment for CLL/SLL is a different pill called venetoclax. The purpose of this study is to compare continuing the current treatment with BTKi alone, as long as it is working, to another arm of treatment which adds venetoclax to the current treatment (BTKi), for one year. After one year, both pills in this arm of treatment would be stopped and the participants will be closely monitored.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 80
Healthy Volunteers: f
View:

• CLL or SLL diagnosis

• Patients must have been diagnosed with CLL (\> 5000 B-cells per uL of peripheral blood at any point during the course of their disease) or small lymphocytic lymphoma (SLL) with \<5000 B-cells per µL of blood but with disease-associated lymphadenopathy by 2018 IWCLL criteria.

• Prior treatment

• Patients must be currently receiving CLL/SLL directed therapy with a BTKi (i.e., ibrutinib, acalabrutinib, zanubrutinib) for at least six months.

• The dose of BTKi must be stable for at least the past three months.

• Age 18 years

• ECOG performance status 0-2

• Detectable or measurable CLL/SLL in blood or imaging during the screening period.

⁃ Detectable CLL/SLL in the blood is defined either by elevation in absolute lymphocyte count or by diagnostic flow cytometry from blood demonstrating presence of CLL cells.

• Low TLS risk, defined as having all lymph nodes less than 5 cm in diameter (radiographically) and absolute lymphocyte count less than 25 x 109/L in blood, within 30 days of enrollment.

• Required initial laboratory values

• Absolute Neutrophil Count (ANC) 1,000/mm3 except if due to bone marrow involvement

• Platelet Count (untransfused) 30,000/mm3 except if due to bone marrow involvement

• Calc. Creatinine Clearance 40 mL/min (by Cockcroft-Gault)

• Bilirubin 1.5 x upper limit of normal (ULN) except if due to liver involvement, hemolysis, or Gilbert's disease

• AST / ALT 2.5 x upper limit of normal (ULN) except if due to liver involvement

• Other

• Patients must be able to swallow oral medications and not have the following conditions: disease significantly affecting gastrointestinal absorption, resection of the stomach or small bowel, partial or complete bowel obstruction.

• Patients must be able to receive either a xanthine oxidase inhibitor or rasburicase

Locations
United States
California
San Francisco VA Medical Center, San Francisco, CA
RECRUITING
San Francisco
Missouri
Kansas City VA Medical Center, Kansas City, MO
RECRUITING
Kansas City
North Carolina
Durham VA Medical Center, Durham, NC
RECRUITING
Durham
Washington
VA Puget Sound Health Care System Seattle Division, Seattle, WA
RECRUITING
Seattle
Contact Information
Primary
Suman Kambhampati, MD MBBS
suman.kambhampati@va.gov
(816) 922-2755
Backup
Murali K Nittala, MBBS MS MD
murali.nittala@va.gov
(816) 861-4700
Time Frame
Start Date: 2025-10-01
Estimated Completion Date: 2030-12-31
Participants
Target number of participants: 100
Treatments
Active_comparator: Arm A : Continue BTKi single agent
Continue BTKi single agent (monotherapy) Standard Intervention
Experimental: Arm B : BTKi + Venetoclax for 12 cycles, then discontinue
BTKi + Venetoclax for 12 cycles, then discontinue Experimental Intervention
Sponsors
Leads: VA Office of Research and Development

This content was sourced from clinicaltrials.gov

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