drugset / Trial / NCT05169515

A Study Evaluating the Safety, Pharmacokinetics, and Efficacy of Mosunetuzumab or Glofitamab in Combination With CC-220 and/or CC-99282 in Participants With B-Cell Non-Hodgkin Lymphoma

NCT05169515

Phase 1 Recruiting 121 enrolled Hoffmann-La Roche
RandomizedParallel-groupOpen-labelTreatment

Summary

This study will evaluate the safety, efficacy, and pharmacokinetics of mosunetuzumab or glofitamab in combination with CELMoDs (CC-220 and/or CC-99282) in participants with B-cell NHL.

Timeline

Start
2022-10-26
Primary completion
2029-09-15
Completion
2029-09-15

Drugs

EvaluationDrugModalityDoseRoute
Subject Glofitamab Monoclonal antibody Intravenous
Subject Golcadomide Other / unclassified Oral
Subject Iberdomide Small molecule Oral
Subject Mosunetuzumab Monoclonal antibody Subcutaneous
Background Obinutuzumab Monoclonal antibody Intravenous
Background Tocilizumab Monoclonal antibody Intravenous