Navy General Hospital
Beijing, Beijing Municipality, 100048, China
Location status: Recruiting
NCT Number: NCT06664411
The goal of this phase 2 trial is to test the safety and efficacy of Pola-ZR2P as induction therapy in patients with DLBCL.
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Request Info14 year and older
All sexes
Interventional
Phase 2
Beijing, Beijing Municipality, 100048, China
Location status: Recruiting
The investigators will evaluate safety and efficacy of Pola-ZR2P as induction therapy in Previously Untreated Diffuse Large B-Cell Lymphoma. ORR(Overall response rate, progression-free survival (PFS), overall survival (OS), adverse events (AEs) will be assessed.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Patients 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
Other names: Pola-ZR2P
Time frame: 2 years
Progression was defined according to the Lugano Response Criteria
Time frame: through study completion, an average of 2 years
OS was defined as time from diagnosis to death from any cause or the last follow-up
Time frame: 1 year
ORR was defined as the proportion of patients who achieved CR or PR
Contact information is provided by the study sponsor or research team.
Navy General Hospital, Beijing
Other
Polatuzumab Vedotin, Zanubrutinib, Rituximab, Lenalidomide and Prednisone in Previously Untreated Diffuse Large B-Cell Lymphoma
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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