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NCT06970743RECRUITINGanonymous

A Phase 3, Open-Label, Randomized Study of BGB-16673 Compared to Investigator's Choice in Patients With Relapsed/Refractory Chronic Lymphocytic Leukemia or Small Lymphocytic Lymphoma Previously Exposed to Covalent BTK Inhibitors

Sponsor

Source record

BeOne Medicines

Phase

Source record

PHASE3

Modality

AI-normalized

small molecule

Target

AI-normalized

BGB-16673, Bendamustine, Rituximab, Methylprednisolone

Indication / condition

AI-normalized

Chronic Lymphocytic Leukemia

Intervention

Source record

BGB-16673, Bendamustine, Rituximab, Methylprednisolone

Source & freshness

Source record

NCT ID

NCT06970743

Original source

ClinicalTrials.gov

Source last updated

May 11, 2026

Ingested at

Jun 05, 2026

Internal sync

Jun 05, 2026

Model version

trialsignal-ai-v1

Normalized confidence

96%

Validation status

validated

Open original registry record
View original source fields

NCT ID

NCT06970743

Title

A Phase 3, Open-Label, Randomized Study of BGB-16673 Compared to Investigator's Choice in Patients With Relapsed/Refractory Chronic Lymphocytic Leukemia or Small Lymphocytic Lymphoma Previously Exposed to Covalent BTK Inhibitors

Sponsor

BeOne Medicines

Status

RECRUITING

Phase

PHASE3

Condition raw

Chronic Lymphocytic Leukemia, Small Lymphocytic Lymphoma

Condition normalized

Chronic Lymphocytic Leukemia, Small Lymphocytic Lymphoma

Modality raw

small molecule

Modality normalized

small molecule

Target raw

BGB-16673, Bendamustine, Rituximab, Methylprednisolone

Target normalized

BGB-16673, Bendamustine, Rituximab, Methylprednisolone

Interventions

BGB-16673, Bendamustine, Rituximab, Methylprednisolone

Public preview

Source record

The purpose of this study is to investigate the efficacy and safety of BGB-16673 compared with investigator's choice (bendamustine plus rituximab or high-dose methylprednisolone plus rituximab) in participants with relapsed/refractory (R/R) chronic lymphocytic leukemia (CLL) or small lymphocytic lymphoma (SLL) previously exposed to covalent Bruton tyrosine kinase inhibitor(s) (cBTKi).

AI-generated analysis supports research triage only. Verify source records, publications, sponsor disclosures and IP databases before making diligence decisions. Model: trialsignal-ai-v1.

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TrialSignal

Clinical trial intelligence report

A Phase 3, Open-Label, Randomized Study of BGB-16673 Compared to Investigator's Choice in Patients With Relapsed/Refractory Chronic Lymphocytic Leukemia or Small Lymphocytic Lymphoma Previously Exposed to Covalent BTK Inhibitors

Source-linked diligence brief with registry provenance, taxonomy normalization and premium analytical context.

Generated

Jun 13, 2026

NCT ID

NCT06970743

Status

RECRUITING

Phase

PHASE3

Sponsor

BeOne Medicines

Executive brief

Investment-Ready Snapshot

The purpose of this study is to investigate the efficacy and safety of BGB-16673 compared with investigator's choice (bendamustine plus rituximab or high-dose methylprednisolone plus rituximab) in participants with relapsed/refractory (R/R) chronic lymphocytic leukemia (CLL) or small lymphocytic lymphoma (SLL) previously exposed to covalent Bruton tyrosine kinase inhibitor(s) (cBTKi).

Source & freshness

Provenance

SourceClinicalTrials.gov
Source updatedMay 11, 2026
Internal syncJun 05, 2026
Model versiontrialsignal-ai-v1

https://clinicaltrials.gov/study/NCT06970743

Indication

Chronic Lymphocytic Leukemia

Modality

small molecule

Target

BGB-16673, Bendamustine, Rituximab, Methylprednisolone

Intervention

BGB-16673, Bendamustine, Rituximab, Methylprednisolone

Source record

Protocol Description

Detailed source ingestion pending.

Source record

Outcome Measures

Detailed source ingestion pending.

Source record

Eligibility

Detailed source ingestion pending.

AI analysis

Known Results And Readout Context

Detailed source ingestion pending.

IP intelligence

Patent And IP Landscape

Detailed source ingestion pending.

Source record

Contacts

Detailed source ingestion pending.