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NCT Number: NCT06669143

Zanubrutinib-based Maintenance Therapy of Newly Diagnosed DLBCL With Initial Remission

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.

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Key information

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Patients were informed about this study and voluntarily signed written informed consent
  • Patients were intolerant first-line intensive chemotherapy, including R-CHOP or R-DA-EPOCH: a) age≧70 years, or unfit or frail according to CGA; b) ECOG 0-2; c) measurable lesions
  • DLBCL with initial CR/PR according to 2016 WHO Classification of Tumor of Haematopoietic and Lymphoid Tissues
  • Life expectancy > 3 months
  • Normal blood count as defined as: absolute neutrophil count ≥1.0 × 10 9 /L independent of growth factor support, platelet count ≥ 100,000/mm 3 or ≥ 50,000/mm 3 if bone marrow (BM) involvement independent of transfusion support in either situation Normal organ functions defined as: creatinine ≤1.5 times the upper limit of normal (ULN) or estimated Glomerular Filtration Rate (Cockroft-Gault) ≥50 ml/min/1.73m 2 , aspartate aminotransferase (AST) or alanine aminotransferase (ALT) ≤2.5× the ULN; total bilirubin ≤ 1.5 × the ULN unless bilirubin rise is due to Gilbert's syndrome or of non-hepatic origin: patients with documented Gilbert disease may be enrolled if total bilirubin is ≤ 3.0 × the ULN;
  • Women of childbearing potential and men who are sexually active must be practicing a highly effective method of birth control during and after the study consistent with local regulations regarding the use of birth control methods for subjects participating in clinical trials. - Women of childbearing potential must have a negative serum (beta-human chorionic gonadotropin [Beta-hCG]) or urine pregnancy test at Screening. Women who are pregnant or breastfeeding are ineligible for this study.

Exclusion criteria

  • Contraindication to any drug in the study
  • Seropositive for or active viral infection with HBV or HCV
  • Human immunodeficiency virus (HIV) infection
  • Any grade 3 or 4 heart disease as defined by the New York Heart Association (NYHA) functional class;
  • QTc (corrected by Fridericia formula): >480ms;
  • Prior malignancies other than lymphoma in the last 5 years with exception of currently treated basal or squamous cell carcinoma or melanoma of the skin or in situ carcinoma of the cervix
  • If female, the patient is pregnant or breast-feeding
  • Any uncontrolled active systemic infection

Treatment and study plan

Zanubrutinib

Drug

160 mg bid, po, day 1-21, a maximum of 2 years.

Lenalidomide

Drug

25 mg qd, po, day 1-10, a maximum of 2 years.

Primary outcomes

  1. 2-year recurrence-free survival

    Time frame: 2 years after enrollment

Secondary outcomes

  1. Overall survival

    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.

  2. Overall response rate

    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)

  3. Complete response rate

    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)

Study contacts

Contact information is provided by the study sponsor or research team.

Weili Zhao, M.D. and Ph.D

CONTACT

[email protected]

021-64370045

Sponsors and collaborators

Lead sponsor

Ruijin Hospital

Other

Registry information

Official study title

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

Important dates

Study start
2024
Primary completion
2026
Study completion
2027
First posted
Nov 1, 2024
Registry last updated
Nov 1, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

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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