Prospective Clinical Study of ZPR Regimen in Relapsed/Refractory Diffuse Large B-cell Lymphoma
- Sponsor
- Peng Liu
- Study ID
- NCT05940051
- Phase
- PHASE2
- Status
- Unknown
Conditions
- Diffuse Large B Cell Lymphoma
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - 80 Years
- Healthy Volunteers
- Not accepted
Interventions
- Zanubrutinib, Polatuzumab vedotin and Rituximab — DRUGZanubrutinib(Z)160 mg bid po Day 1-21; Polatuzumab vedotin(P)1.8 mg/kg ivgtt D1; Rituximab(R)375 mg/m2 ivgtt D1
Study Details
This is a prospective, single-arm, single-center clinical study. This clinical study aims to explore the efficacy and safety of the ZPR(Zanubrutinib, Polatuzumab vedotin and Rituximab)regimen in the treatment of patients with relapsed and refractory diffuse large B-cell lymphoma.
Key Dates
- Start date
- Jul 20, 2023
- Status verified
- Jul 2023
- Primary completion
- Jul 1, 2025
- Completion
- Dec 30, 2025
Study Design
- Enrollment
- 35 participants (estimated)
- Allocation
- NA
- Intervention model
- SINGLE_GROUP
- Primary purpose
- TREATMENT
Arms
- Experimental: R/R Diffuse Large B-cell Lymphoma
Primary Outcome Measure
ORR at the end of the 6th treatment cycle [ Time Frame: about six months from the start of ZPR ]
Central Contacts
- Peng Liu, Ph.D+862164041990
- Yian Zhang, Ph.D+862164041990
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