Recruiting PHASE3 Chronic Lymphocytic Leukemia

Compares treatment options for Chronic Lymphocytic Leukemia

Official title A Study to Investigate Sonrotoclax (BGB-11417) Plus Zanubrutinib (BGB-3111) Compared With Venetoclax Plus Acalabrutinib in Adults With Previously Untreated Chronic Lymphocytic Leukemia

ClinicalTrials.gov ID: NCT07277231

What this study is testing

What is Sonrotoclax?

Sonrotoclax is an investigational medicine, given as a pill taken by mouth, being studied as a potential treatment for chronic lymphocytic leukemia.

Also referred to as BGB-11417.

Plain-language explanation of the investigational treatment - it is being studied and is not an approved or proven therapy. The study team can confirm the details.

What it's testing
The purpose of this study is to investigate the efficacy and safety of fixed-duration sonrotoclax (also known as BGB-11417) plus zanubrutinib (also known as BGB-3111) (SZ) compared with fixed-duration of venetoclax plus acalabrutinib (AV) in participants with previously untreated chronic lymphocytic leukemia (CLL).
  • Phase 3: a large, late-stage study

A plain-language read of the study's public ClinicalTrials.gov listing. The study team confirms the details.

Who can take part

Ages 18 and older

You may be able to join if

  • Treatment-naïve (TN) adults with confirmed diagnosis of CLL which requires treatment
  • Eastern Cooperative Oncology Group (ECOG) score 0, 1, or 2
  • Measurable disease by Computer Tomography/Magnetic Resonance Imaging
  • Adequate bone marrow and organ function

You likely can't join if

  • Previous systemic treatment for CLL
  • Known prolymphocytic leukemia or history of, or currently suspected, Richter's transformation
  • Known central nervous system involvement
  • History of confirmed progressive multifocal leukoencephalopathy (PML)
  • Uncontrolled hypertension or clinically significant cardiovascular disease Note: Other protocol defined Inclusion/Exclusion criteria may apply.

The study team makes the final eligibility decision.

Where it's taking place

  • Palo Alto, California, United States
  • Seattle, Washington, United States
  • Blacktown, New South Wales, Australia
  • Concord, New South Wales, Australia
  • St Leonards, New South Wales, Australia
  • Woolloongabba, Queensland, Australia
  • Clayton, Victoria, Australia
  • Heidelberg, Victoria, Australia
  • Malvern, Victoria, Australia
  • Melbourne, Victoria, Australia
  • Brasília, Brazil
  • Porto Alegre, Brazil
  • São Paulo, Brazil
  • Victoria, British Columbia, Canada
  • Hamilton, Ontario, Canada
  • Montreal, Quebec, Canada
  • Sherbrooke, Quebec, Canada
  • Québec, Canada
  • Beijing, Beijing Municipality, China
  • Chongqing, Chongqing Municipality, China

+ 64 more site(s).

Questions & answers

Do participants get paid in this trial?

This listing doesn't specify compensation. Many trials still reimburse travel or offer a stipend, so it's worth asking the study team when you connect.

Is it free to join, and do I need insurance?

Searching and applying through BridgeMD is free. In clinical trials the study-related treatment and visits are generally provided at no cost to you. You usually don't need insurance to take part - confirm specifics with the study team.

How long does this study last?

The listing doesn't state an exact length. The study team walks you through the schedule and number of visits before you decide to enroll.

Who can join this trial?

This study is enrolling all sexes, 18 years and older. The study team makes the final eligibility decision.

Where is this trial taking place?

Study sites include Palo Alto, California, United States; Seattle, Washington, United States; Blacktown, New South Wales, Australia; Concord, New South Wales, Australia; St Leonards, New South Wales, Australia; Woolloongabba, Queensland, Australia and 78 more location(s). Enter your location above to see the nearest site and check your eligibility.

Explore other conditions

BridgeMD is an information and trial-matching tool - not medical advice, and not the study sponsor. Details come from ClinicalTrials.gov; the study team decides eligibility.