RecruitingPhase 2NCT06967610

Phase II Study of Combined Pirtobrutinib, Venetoclax and Obinutuzumab (PVO) Time-limited Treatment for Patients With Recurrent Chronic Lymphocytic Leukemia/Small Lymphocytic Lymphoma (CLL/SLL).


Sponsor

M.D. Anderson Cancer Center

Enrollment

40 participants

Start Date

Jul 15, 2025

Study Type

INTERVENTIONAL

Conditions

Summary

To learn if the drug combination pirtobrutinib, venetoclax, and obinutuzumab can help to control relapsed CLL/SLL.


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This study is testing a three-drug combination — pirtobrutinib, venetoclax, and obinutuzumab — for people with chronic lymphocytic leukemia (CLL) or small lymphocytic lymphoma (SLL) whose cancer has come back or stopped responding to previous treatments. **You may be eligible if...** - You are 18 or older with a confirmed diagnosis of CLL or SLL - You have already received treatment for CLL/SLL and need further therapy - You can swallow oral medications - Your kidneys, liver, and bone marrow are functioning adequately - You are in reasonably good physical health (able to care for yourself) **You may NOT be eligible if...** - Your cancer progressed while you were taking venetoclax - You have a history of Richter's syndrome (a transformation of CLL into a more aggressive lymphoma) - You have not had sufficient time (washout period) since your last cancer treatment - You are pregnant or planning to become pregnant without using effective contraception 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.

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Interventions

DRUGPirtobrutinib

Given PO 200mg daily

DRUGVenetoclax

Given PO daily

DRUGObinutuzumab

Given IV 100mg day 1, 900 mg day 2, 100mg days 8, 15


Locations(1)

MD Anderson Cancer Center

Houston, Texas, United States

View Full Details on ClinicalTrials.gov

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NCT06967610


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