Trials / Not Yet Recruiting
Not Yet RecruitingNCT07299331
Zanubrutinib, Rituximab, and Lenalidomide in the First-Line Treatment of Marginal Zone Lymphoma
A Multicenter, Single-Arm, Prospective Clinical Study of Zanubrutinib, Rituximab, and Lenalidomide in the First-Line Treatment of Marginal Zone Lymphoma
- Status
- Not Yet Recruiting
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 50 (estimated)
- Sponsor
- Zhengzhou University · Academic / Other
- Sex
- All
- Age
- 18 Years – 75 Years
- Healthy volunteers
- Not accepted
Summary
The goal of this clinical trial is to learn if Zanubrutinib, Rituximab, and Lenalidomide works to treat marginal zone lymphoma as the first-line therapy. It will also learn about the safety of the treatment. The main questions it aims to answer are Does the combined therapy prolong patient survival? What medical problems do participants have when using this therapeutic approach? Researchers will observe the treatment to see if it works well than conventional therapies. Participants will Administer drugs as required by the protocol Visit the clinic regularly for checkups and tests Keep a diary of their symptoms, examination and laboratory test indicators
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Zanubrutinib, Rituximab, and Lenalidomide as first-line treatment for Marginal Zone Lymphoma | This study enrolls patients with marginal zone lymphoma who require the primary treatment. Participants receive a combined therapy consisting of zanubrutinib, rituximab, and lenalidomide. |
| DRUG | Zanubrutinib, Rituximab, and Lenalidomide as the primary treatment for Marginal Zone Lymphoma | This study enrolls patients with marginal zone lymphoma who require the primary treatment. Participants receive a combined therapy consisting of zanubrutinib, rituximab, and lenalidomide. |
Timeline
- Start date
- 2026-01-01
- Primary completion
- 2031-04-30
- Completion
- 2031-04-30
- First posted
- 2025-12-23
- Last updated
- 2025-12-23
Source: ClinicalTrials.gov record NCT07299331. Inclusion in this directory is not an endorsement.