drugset / Trial / NCT06558604
Phase II Study of Glofitamab With Venetoclax +/- Zanubrutinib in High-risk Mantle-cell Lymphoma
Phase 2
Recruiting
100 enrolled
The Lymphoma Academic Research Organisation
BeiGene · collabHoffmann-La Roche · collab
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| 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 |