RecruitingPhase 4NCT07270835

Zanubrutinib Combined With Rituximab in the Treatment of Secondary HLH in B-cell Lymphoma

The Study of Zanubrutinib Combined With Rituximab in the Treatment of Secondary Hemophagocytic Lymphohistiocytosis in B-cell Lymphoma


Sponsor

The First Affiliated Hospital of Soochow University

Enrollment

40 participants

Start Date

Nov 1, 2025

Study Type

INTERVENTIONAL

Conditions

Summary

For patients who met the inclusion criteria, treatment regimens were administered: Rituximab 375 mg/m², intravenously, once weekly for 4 weeks. Zanubrutinib 160 mg, orally, twice daily for 4 weeks. Combined drugs: prednisone 100 mg/m²/d, orally, d1-5; Ruxolitinib 15mg bid orally; With/without emapalumab as appropriate.


Eligibility

Min Age: 14 YearsMax Age: 80 Years

Plain Language Summary

Simplified for easier understanding

This study is testing a combination of two drugs — zanubrutinib (a targeted cancer pill) and rituximab (an IV infusion) — for treating a rare and life-threatening condition called hemophagocytic lymphohistiocytosis (HLH) that occurs in patients with B-cell lymphoma. HLH is a severe immune overreaction that can be triggered by lymphoma. **You may be eligible if...** - You meet the standard diagnostic criteria for HLH - Your HLH is associated with a confirmed or strongly suspected B-cell lymphoma - You are between 14 and 80 years old - You are HIV-negative - Your kidney function and other labs are within acceptable ranges **You may NOT be eligible if...** - You have HLH from a cause other than B-cell lymphoma - You are HIV-positive - You have severe kidney or liver dysfunction - Your expected survival is less than one month - You are pregnant or breastfeeding Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DRUGRituximab

375 mg/m², intravenously, once weekly for 4 weeks

DRUGZanubrutinib

160 mg, orally, twice daily for 4 weeks as for rutuximab.


Locations(1)

The First Affiliated Hospital of Soochow University

Suzhou, Jiangsu, China

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NCT07270835