RecruitingPhase 2NCT07014917

Intermittent Versus Continuous Venetoclax With Acalabrutinib for CLL/SLL

Randomized Phase II Study of Intermittent Versus Continuous Venetoclax Therapy With Acalabrutinib in Previously Untreated Chronic Lymphocytic Leukemia/Small Lymphocytic Lymphoma (CLL/SLL) and Variants of This


Sponsor

Zulfa Omer

Enrollment

62 participants

Start Date

Dec 5, 2025

Study Type

INTERVENTIONAL

Conditions

Summary

This is a randomized Phase II study of intermittent versus continuous venetoclax therapy with Acalabrutinib in previously untreated Chronic Lymphocytic Leukemia/Small Lymphocytic Lymphoma (CLL/SLL)


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This study is comparing two treatment approaches for previously untreated chronic lymphocytic leukemia (CLL) or small lymphocytic lymphoma (SLL): one where venetoclax is given continuously alongside acalabrutinib, versus one where venetoclax is given in on/off cycles to potentially reduce side effects while maintaining effectiveness. **You may be eligible if...** - You are 18 or older with a confirmed new diagnosis of CLL or SLL that requires treatment - You have never been treated for CLL or SLL before - Your general health is good enough to participate (ECOG score 0, 1, or 2) - Your kidney, liver, and blood counts meet minimum thresholds **You may NOT be eligible if...** - You have previously received any treatment for CLL or SLL - You are pregnant or breastfeeding - You have certain heart rhythm problems or significant organ dysfunction - You are on certain medications that interact with the study drugs Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

Interested in this trial?

Get notified about updates and connect with the research team.

Interventions

DRUGVenetoclax

intermittent venetoclax (7days administration per cycle) + acalabrutinib

DRUGAcalabrutinib

intermittent venetoclax (7days administration per cycle) + acalabrutinib

DRUGVenetoclax

continuous venetoclax (28 days administrations per cycle) + acalabrutinib

DRUGAcalabrutinib

continuous venetoclax (28 days administrations per cycle) + acalabrutinib


Locations(1)

University of Cincinnati

Cincinnati, Ohio, United States

View Full Details on ClinicalTrials.gov

For the most up-to-date information, visit the official listing.

Visit

NCT07014917


Related Trials