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A Phase 3, Randomized Study to Compare Nemtabrutinib Versus Comparator (Investigator’s Choice of Ibrutinib or Acalabrutinib) in Participants With Untreated Chronic Lymphocytic Leukemia/Small Lymphocytic Lymphoma (BELLWAVE-011)

Status
Withdrawn
Phases
Phase 3
Study type
Interventional
Source
EU CTIS
Registry ID
CTIS2022-501697-19-00
Acronym
MK-1026-011
Enrollment
50
Registered
2024-01-22
Start date
Unknown
Completion date
Unknown
Last updated
2024-01-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Small Lymphocytic Lymphoma (SLL) / Untreated Chronic Lymphocytic Leukemia (CLL)

Brief summary

Objective Response Rate (ORR) per Chronic Lymphocytic Leukemia (iwCLL) Criteria 2018 as assessed by Blinded Independent Central Review (BICR), Progression-Free Survival (PFS) per iwCLL Criteria 2018 as assessed by BICR

Detailed description

Overall Survival (OS), Duration of Response (DOR) per iwCLL Criteria 2018 as assessed by BICR, Number of Participants Who Experience One or More Adverse Events (AEs), Number of Participants Who Discontinue Study Treatment Due to an AE

Interventions

DRUGNemtabrutinib
DRUGACALABRUTINIB
DRUGIBRUTINIB

Sponsors

Merck Sharp & Dohme LLC
Lead SponsorINDUSTRY

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Design outcomes

Primary

MeasureTime frame
Objective Response Rate (ORR) per Chronic Lymphocytic Leukemia (iwCLL) Criteria 2018 as assessed by Blinded Independent Central Review (BICR), Progression-Free Survival (PFS) per iwCLL Criteria 2018 as assessed by BICR

Secondary

MeasureTime frame
Overall Survival (OS), Duration of Response (DOR) per iwCLL Criteria 2018 as assessed by BICR, Number of Participants Who Experience One or More Adverse Events (AEs), Number of Participants Who Discontinue Study Treatment Due to an AE

Countries

Spain

Outcome results

None listed

Source: EU CTIS · Data processed: Feb 4, 2026