A Study to Evaluate the Safety and Efficacy of BGB-16673 Compared to Pirtobrutinib in Adults With Relapsed/Refractory Chronic Lymphocytic Leukemia or Small Lymphocytic Lymphoma
Part of paid clinical trials in Phoenix, Arizona.
- Sponsor
- BeOne Medicines
- Study ID
- NCT06973187
- Phase
- PHASE3
- Status
- Recruiting
Conditions
- Chronic Lymphocytic Leukemia
- Small Lymphocytic Lymphoma
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- BGB-16673 — DRUGBGB-16673 will be administered orally
- Pirtobrutinib — DRUGPirtobrutinib will be administered orally
Study Details
The purpose of this study is to evaluate the efficacy and safety of BGB-16673 alone compared with pirtobrutinib in patients with relapsed or refractory (R/R) chronic lymphocytic leukemia (CLL) or small lymphocytic lymphoma (SLL) who had been previously treated with a covalent Bruton tyrosine kinase inhibitor (cBTKi).
Key Dates
- Start date
- Sep 4, 2025
- Status verified
- Jun 2026
- Primary completion
- Apr 17, 2028
- Completion
- Apr 17, 2028
Study Design
- Enrollment
- 500 participants (estimated)
- Allocation
- RANDOMIZED
- Intervention model
- PARALLEL
- Primary purpose
- TREATMENT
Arms
- Experimental: Arm A: BGB-16673Participants will receive BGB-16673 orally.
- Active Comparator: Arm B: PirtobrutinibParticipants will receive pirtobrutinib orally.
Primary Outcome Measure
Progression-Free Survival (PFS) per Independent Review Committee (IRC) [ Time Frame: Up to approximately 3 years ]
Central Contacts
- Study Director1-877-828-5568
Locations (36)
Find similar trials in Phoenix, AZ
By condition
By specialty
By research site
Mayo Clinic Phoenix· Phoenix, AZKaiser Permanente Southern California· Irvine, CAUniversity of California San Diego (Ucsd) Moores Cancer Center· La Jolla, CACancer and Blood Specialty Clinic· Los Alamitos, CAUCLA Department of Medicine Hematologyoncology· Los Angeles, CAStanford Cancer Institute· Palo Alto, CA
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