Ongoing BsAb trials in MCL (including for previously untreated patients)
| Setting . | Agent(s) . | NCT . | Geography . | Notes . |
|---|---|---|---|---|
| R/R | Epcoritamab, ibrutinib | NCT05283720 | Global | |
| R/R | Epcoritamab, ibrutinib, venetoclax | |||
| Treatment naïve | Epcoritamab, ibrutinib, venetoclax | |||
| R/R | Glofitamab, lenalidomide | NCT06192888 | United States | Prior BTKi mandatory; prior lenalidomide acceptable if >12 months interval since treatment and previously sensitive |
| R/R | Glofitamab, pirtobrutinib | NCT05833763 | Australia | Prior BTKi mandatory |
| NCT06252675 | United States | Must have responded to prior BTKi therapy | ||
| Treatment naïve | Glofitamab, ibrutinib | NCT06357676 | United States | Either high-risk disease or ≥65 years old |
| R/R | Acalabrutinib, obinutuzumab, and glofitamab | NCT06054776 | United States | Incorporates measurable residual disease testing |
| Treatment naïve | Glofitamab, obinutuzumab, venetoclax, and lenalidomide | NCT05861050 | United States | At least one high-risk disease feature must be present |
| R/R | Glofitamab vs investigator's choice (rituximab-lenalidomide or rituximab-bendamustine) | NCT06084936 | Global | Prior BTKi mandatory |
| Mosunetuzumab | NCT05207670 | United States | Prior BTKi mandatory | |
| Mosunetuzumab – polatuzumab-vedotin | NCT03671018 | United States, Europe | ≥2 prior lines of systemic therapy including BTKi, anti-CD20 MAb, and chemotherapy |
| Setting . | Agent(s) . | NCT . | Geography . | Notes . |
|---|---|---|---|---|
| R/R | Epcoritamab, ibrutinib | NCT05283720 | Global | |
| R/R | Epcoritamab, ibrutinib, venetoclax | |||
| Treatment naïve | Epcoritamab, ibrutinib, venetoclax | |||
| R/R | Glofitamab, lenalidomide | NCT06192888 | United States | Prior BTKi mandatory; prior lenalidomide acceptable if >12 months interval since treatment and previously sensitive |
| R/R | Glofitamab, pirtobrutinib | NCT05833763 | Australia | Prior BTKi mandatory |
| NCT06252675 | United States | Must have responded to prior BTKi therapy | ||
| Treatment naïve | Glofitamab, ibrutinib | NCT06357676 | United States | Either high-risk disease or ≥65 years old |
| R/R | Acalabrutinib, obinutuzumab, and glofitamab | NCT06054776 | United States | Incorporates measurable residual disease testing |
| Treatment naïve | Glofitamab, obinutuzumab, venetoclax, and lenalidomide | NCT05861050 | United States | At least one high-risk disease feature must be present |
| R/R | Glofitamab vs investigator's choice (rituximab-lenalidomide or rituximab-bendamustine) | NCT06084936 | Global | Prior BTKi mandatory |
| Mosunetuzumab | NCT05207670 | United States | Prior BTKi mandatory | |
| Mosunetuzumab – polatuzumab-vedotin | NCT03671018 | United States, Europe | ≥2 prior lines of systemic therapy including BTKi, anti-CD20 MAb, and chemotherapy |