BrUOG 401: A Phase 2 Study of Mosunetuzumab With Lenalidomide Augmentation as First-line Therapy for Follicular and Marginal Zone Lymphoma
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What is the purpose of this trial?
BrUOG-401 is a prospective, single-arm, phase 2 trial of first-line therapy in adult patients with previously untreated FL or MZL. All patients will be assigned the same initial treatment plan, modified by interim response assessment (IRA) after Cycle 4. All patients will start treatment with four 21-day cycles (C1-4) of mosunetuzumab alone (using step-up dosing during C1), followed by IRA. Patients who achieve CR at IRA will continue with additional 4 cycles (C5-8) of mosunetuzumab. Patients who achieve PR at IRA will receive mosunetuzumab with lenalidomide augmentation during C5-8. Primary response assessment (PRA) will occur after C8. Patients who remain in PR at PRA will continue for additional 4 cycles (extended augmentation).
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Principal Investigator
Sub-Investigators
- Agatha Hecht
- Alessia Donadio, MD
- Alfredo Axtmayer
- Alison Johnson
- Brooke Chaves
- Catherine Wei, MD
- David Witt, MD
- Elizabeth Cappiello
- Emily Collier, MD
- Ethan Kohn
- Francine Foss, MD
- Iris Isufi, MD
- James Vredenburgh, MD
- Jean Vollmer
- Jose Morales-Marin
- Kaitlin Brown
- Karishma Mehra, MBBS
- Larisa Fleysher
- Laura Sabourin
- Leena Rahmat
- Madeleine Wood
- Neal Fischbach, MD
- Pawan Karanam, MD
- Renee Moye
- Shalin Kothari, MD
- Stuart Seropian, MD
- Sudhanshu Mulay, MD
- Syed Ali
- Syed Bilgrami, MBBS
- Tarsheen Sethi, MD, MSc
- Vidya Kesavan
- Zia Rahman, MD
- Last Updated12/08/2024
- Study HIC#2000031398