drugset / Trial / NCT06558604

Phase II Study of Glofitamab With Venetoclax +/- Zanubrutinib in High-risk Mantle-cell Lymphoma

NCT06558604

Non-randomizedParallel-groupOpen-labelTreatment

Summary

This open-label, multicenter, three cohorts, phase II study is designed to assess a combination of Zanubrutinib/Venetoclax/Glofitamab or Venetoclax/Glofitamab in high-risk subjects with either first line or R/R Mantle Cell Lymphoma (MCL). Three independent cohorts will be run: * Cohort A will include subjects with a primary refractory or progressive disease within 24 months from initiation of first line treatment (POD 24). * Cohort B will be open for subjects with R/R MCL and refractory or progressive to a BTK inhibitor given previously (\>24 months if first line). * Cohort C will only enrol newly diagnosed and untreated MCL subjects with very high-risk features.

Timeline

Start
2025-02-21
Primary completion
2028-05
Completion
2032-03

Drugs

EvaluationDrugModalityDoseRoute
Subject Glofitamab Monoclonal antibody 30 mg Intravenous
Subject Obinutuzumab Monoclonal antibody 1000 mg Intravenous
Subject Obinutuzumab Monoclonal antibody 2000 mg Intravenous
Subject Venetoclax Small molecule 400 mg Oral
Subject Zanubrutinib Small molecule 320 mg Oral

Indications