Zanubrutinib Plus R-CHOP for Patients With Newly Diagnosed Untreated Non-GCB DLBCL
- Sponsor
- The First Affiliated Hospital of Soochow University
- Study ID
- NCT04835870
- Phase
- PHASE2
- Status
- Unknown
Conditions
- Non-GCB/ABC Diffuse Large B-Cell Lymphoma
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- Zanubrutinib — DRUGZanubrutinib-160mg bid PO d0-d20(1-21d)
- Rituximab — DRUGRituximab-375 mg/m2 i.v d0 (/21d)
- Cyclophosphamide — DRUGCyclophosphamide-750 mg/m2 i.v d1 (/21d)
- Doxorubicin — DRUGDoxorubicin-50 mg/m2 i.v d1 (/21d)
- Vincristine — DRUGVincristine-1.4 mg/m2 i.v d1 (/21d)(2 mg max)
- Prednisone — DRUGPrednisone-100 mg p.o d1-d5 (/21d)
Study Details
Aim of this study will evaluate the efficacy and safety of zanubrutinib in combination with R-CHOP for newly diagnosed untreated Non-GCB DLBCL Patients
Key Dates
- Start date
- Apr 1, 2021
- Status verified
- Mar 2022
- Primary completion
- Oct 1, 2025
- Completion
- Oct 1, 2025
Study Design
- Enrollment
- 78 participants (estimated)
- Allocation
- NA
- Intervention model
- SINGLE_GROUP
- Primary purpose
- TREATMENT
Arms
- Experimental: R-CHOP + ZanubrutinibZanubrutinib plus Rituximab, Cyclosphosphamide, Doxorubicin, Vincristine and Prednisone (R-CHOP)
Primary Outcome Measure
Progression-free Survival(PFS) [ Time Frame: up to 18 months ]
Central Contacts
- Caixia Li, M.D+86 512 67781856
- Jia Chen, M.D+86 512 67781856