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

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NCT07277231 · readout ≤ 1,654 d

Sponsored by BeOne Medicines (industry) · ONC — their whole pipeline →.

Phase
Phase 3
Status
Recruiting
Study type
Interventional
Design
Randomized · None · Treatment
Enrollment
500estimated
Sites
105
Countries
Australia, Brazil, Canada +14

Every value on this page is a field the sponsor filed with ClinicalTrials.gov, reproduced. Dates are their own estimates, revised as a study runs, unless the registry marks them actual. sources →

Source: ClinicalTrials.gov, retrieved 2026-08-19

Dates

each axis at the precision it was filed, with the registry's own basis
DateFiledBasisWhat it is
Start2026-01-22actualWhen the study began enrolling
Primary completionFeb 2031estimatedThe date the last participant is measured for the primary outcome — the readout window
Study completionNov 2031estimatedThe whole study's end, after follow-up
First posted2025-12-11actualWhen this record first appeared on the registry
Results postedWhen the sponsor posted results to the registry
Record updated2026-08-19actualThe sponsor's own last edit to this record — every projection above is as current as this date

What it studies

Condition

  • Chronic Lymphocytic Leukemia

Interventions

  • Drug: Sonrotoclax — also filed as BGB-11417
  • Drug: Zanubrutinib — also filed as BGB-3111, Brukinsa
  • Drug: Acalabrutinib — also filed as Calquence
  • Drug: Venetoclax — also filed as Venclexta, Venclyxto

Primary outcomes

what the primary-completion date above is the date OF
Progression-Free Survival (PFS) as Determined by Independent Review Committee (IRC)
measured Up to approximately 70 months
Rate of Undetectable Minimal Residual Disease at < 10^-4 sensitivity (uMRD4)
measured Up to approximately 16 months

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