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Taking people in ChinaPhase 2

Zanubrutinib and lenalidomide as maintenance treatment for diffuse large B-cell lymphoma

Tests two drugs as maintenance treatment in people with diffuse large B-cell lymphoma.

Plain-language title generated from the registry record
Registry title: Zanubrutinib and Lenalidomide as Maintenance Therapy in DLBCL

Key facts

Where
Beijing, ChinaSee the site
Phase
Phase 2

Where in China

  • Navy General HospitalBeijing, ChinaTaking people

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?
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Trial details

Who runs it
Navy General Hospital, Beijing
Trial code
NCT06503263
Record updated
19 September 2024
Original description
The goal of this phase 2 trial is to test the safety and efficacy of zanubrutinib and lenalidomide as maintenance therapy in patients with DLBCL.Read full original descriptionShow less

Zanubrutinib and Lenalidomide as Maintenance Therapy in Patients With Diffuse Large B-cell Lymphoma

The goal of this phase 2 trial is to test the safety and efficacy of zanubrutinib and lenalidomide as maintenance therapy in patients with DLBCL.

Inclusion: Pathologically confirmed Diffuse Large B Cell Lymphoma according World Health Organization (WHO) classification; Patient is ≥ 18 years of age at the time of signing the informed consent form (ICF); Patient must understand and voluntarily sign an ICF prior to any study-specific assessments/procedures being conducted; Patient is willing and able to adhere to the study visit schedule and other protocol requirements; Patient has recieved complete remission and has completed planed courses of chemotherapy; Meet the following lab criteria: Absolute Neutrophil Count (ANC) ≥ 1,5 x 10\^9/L (≥ 1 x 10\^9/L if bone marrow (BM) involvement by lymphoma);Platelet ≥ 75 x 10\^9/L (≥ 50 x 10\^9/L if BM involvement by lymphoma); Hemoglobin ≥ 8 g/dL. Anticipated life expectancy at least 3 months.

Exclusion: Active or uncontrolled infections requiring systemic treatment within 14 days before enrollment; Any instability of systemic disease, including but not limited to severe cardiac, liver, kidney, or metabolic disease need therapy; Pregnant or lactating women.

ClinicalTrials.gov NCT06503263