Pola-ZR2P in Previously Untreated DLBCL
- Sponsor
- Navy General Hospital, Beijing
- Study ID
- NCT06664411
- Phase
- PHASE2
- Status
- Recruiting
Conditions
Eligibility Criteria
- Sex
- ALL
- Age
- 14 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- Polatuzumab Vedotin, Zanubrutinib, Rituximab, Lenalidomide and Prednisone as Induction Therapy — DRUGPatients were treated by Polatuzumab Vedotin(1.8mg/kg iv qd d1), Zanubrutinib(160mg po bid d1-21), Rituximab(375mg/m2 iv qd d1), Lenalidomide(25mg po qd d1-14) and Prednisone(60mg/m2 po qd d1-5) as induction therapy
Study Details
The goal of this phase 2 trial is to test the safety and efficacy of Pola-ZR2P as induction therapy in patients with DLBCL.
Key Dates
- Start date
- Sep 24, 2024
- Status verified
- Aug 2025
- Primary completion
- Dec 31, 2029
- Completion
- Dec 31, 2030
Study Design
- Enrollment
- 80 participants (estimated)
- Allocation
- NA
- Intervention model
- SINGLE_GROUP
- Primary purpose
- TREATMENT
Arms
- Experimental: Pola-ZR2PPatients were treated by Pola-ZR2P as Induction Therapy
Primary Outcome Measure
Progression Free Survival (PFS) [ Time Frame: 2 years ]
Central Contacts
- Liren Qian, PhD+861066947194
- Liren Qian, PhD
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