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Study to Assess Change in Disease Activity and Adverse Events of Oral Venetoclax With Intravenous (IV) Obinutuzumab in Adult Participants With Recurring Chronic Lymphocytic Leukemia (CLL)

Recruiting · Phase 2 · NCT04895436

Conditions: Chronic Lymphocytic Leukemia (CLL)

At a glance

Research payments reported, 2025
$214,177
U.S. investigators named
9
Sites paid
9
Planned or actual enrollment
75

About the trial

Sponsor
AbbVie (with F. Hoffmann-La Roche Ltd, German CLL Study Group (GCLLSG), Dana-Farber Cancer Institute)
Tested
Venetoclax (drug), Obinutuzumab (drug)
Dates
Started 2022-03-28; completion 2029-01
Results posted
Not yet

Chronic lymphocytic leukemia (CLL) is the most common leukemia (cancer of blood cells). The purpose of this study is to assess retreatment with venetoclax-obinutuzumab (VenG) in participants previously treated with fixed duration first-line (IL) therapy of venetoclax in combination with an anti-CD20 antibody +/- X (where X is any additional drug). Adverse events and change in disease activity will be assessed. Venetoclax is an approved drug for the treatment of CLL. Study doctors put the participants in 1 of 2 groups, called cohorts, based on when symptoms of CLL came back after previous treatment in first-line. Approximately 75 adult participants with CLL who have been treated with venet…

From ClinicalTrials.gov, last updated 2026-02-09. Full record, eligibility and contacts (opens in a new tab)

Industry funding

AbbVie Inc. reported $214,177 in research payments for this study in 2025 (29 payments).

Products named: Venclexta

Research payments usually go to hospitals, universities and research sites to run a study, not to the investigators personally. A payment is not evidence of wrongdoing.

U.S. investigators named on this study

Clinicians the company named as principal investigators in its Open Payments reports.

Sites paid to run it

Sources: CMS Open Payments research payments (program year 2025) and ClinicalTrials.gov, U.S. National Library of Medicine.