drugset / Trial / NCT06244368

Summary

This is a prospective clinical study to evaluate the safety and efficacy of GVM±R in patients with relapsed or refractory aggressive non-Hodgkin's lymphoma (NHL).

Timeline

Start
2024-01-17
Primary completion
2025-12-30
Completion
2027-12-30

Drugs

EvaluationDrugModalityDoseRoute
Subject Mitoxantrone Small molecule 18 mg/m2
Subject Rituximab Monoclonal antibody 375 mg/m2
Background Gemcitabine Small molecule 800 mg/m2
Background Vinorelbine Small molecule 20 mg/m2