Zanubrutinib
Drug160 mg bid, po, day 1-21, a maximum of 2 years.
NCT Number: NCT06669143
This single-arm, prospective clinical study will evaluate the efficacy and safety of Zanubrutinib-based maintenance therapy for post-remission in newly diagnosed DLBCL who are intolerant to first-line intensive chemotherapy.
Trial opening soon.
Get Notified70 year and older
All sexes
Interventional
Phase 2
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
160 mg bid, po, day 1-21, a maximum of 2 years.
25 mg qd, po, day 1-10, a maximum of 2 years.
Time frame: 2 years after enrollment
Time frame: From enrollment to study completion, a maximum of 4.5 years
Overall survival was defined as the time from the date of enrollment to the date of death from any cause.
Time frame: up to 2 year, at the end of maintenance
ORR at treatment completion or discontinuation defined as the proportion of participants with partial response (PR) or CR at the end of treatment according to the 2014 Lugano Response Criteria; as determined by the investigator and IRC(separately)
Time frame: up to 2 year, at the end of maintenance
CR rate at the end of treatment by FDG-PET defined as the proportion of participants with CR at the end of treatment according to the 2014 Lugano Response Criteria; as determined by the investigator and IRC (separately)
Contact information is provided by the study sponsor or research team.
Ruijin Hospital
Other
The Efficacy and Safety of Zanubutinib-based for Post-remission Maintenance in Patients With Diffuse Large B-cell Lymphoma Who Are Intolerant to Intense First-line Chemotherapy
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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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