Mosunetuzumab With Lenalidomide Augmentation as First-line Therapy for Follicular and Marginal Zone Lymphoma

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 r

Trial Details

NCT ID
NCT04792502
Phase
PHASE2
Sponsor
Brown University
Status
RECRUITING
Cancer Type
Lymphoma
Interventions
  • Mosunetuzumab
  • Lenalidomide
Locations (sample)
  • New Haven, Connecticut, United States|41.30815,-72.92816
  • New Brunswick, New Jersey, United States|40.48622,-74.45182
  • Providence, Rhode Island, United States|41.82399,-71.41283

Key Eligibility Criteria

  • Ability to understand and the willingness to sign a written informed consent document and to comply with the study protocol procedures.
  • Age ≥18 years at the time of signing informed consent. Because no dosing or adverse event data are currently available on the use of mosunetuzumab …
  • Histologically confirmed diagnosis of:
  • follicular lymphoma (grade 1, 2, 3a, or not otherwise specified) or

For full eligibility, visit ClinicalTrials.gov.

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