WHO ICTRP trial

A PHASE II STUDY EVALUATING THE SAFETY AND EFFICACY OF GLOFITAMAB IN COMBINATION…

NL-OMON56027 · Overview of Medical Research in the Netherlands (NL-OMON) · Recruiting

Key facts

Trial ID NL-OMON56027
Public title A PHASE II STUDY EVALUATING THE SAFETY AND EFFICACY OF GLOFITAMAB IN COMBINATION WITH RITUXIMAB (R) PLUS CYCLOPHOSPHAMIDE, DOXORUBICIN, VINCRISTINE, AND PREDNISONE (CHOP) IN CIRCULATING TUMOR (ct)DNA HIGH-RISK PATIENTS WITH UNTREATED DIFFUSE LARGE B-CELL LYMPHOMA
Scientific title A PHASE II STUDY EVALUATING THE SAFETY AND EFFICACY OF GLOFITAMAB IN COMBINATION WITH RITUXIMAB (R) PLUS CYCLOPHOSPHAMIDE, DOXORUBICIN, VINCRISTINE, AND PREDNISONE (CHOP) IN CIRCULATING TUMOR (ct)DNA HIGH-RISK PATIENTS WITH UNTREATED DIFFUSE LARGE B-CELL LYMPHOMA - GO43075
Primary sponsor Roche Nederland B.V.
Registry Overview of Medical Research in the Netherlands (NL-OMON)
Recruitment status Recruiting
Study type Interventional
Phase 2
Countries Denmark;France;Netherlands;Poland;Spain;United States of America
Conditions B-cell lymphoma lymph node cancer;10025320;B-cell lymphoma;lymph node cancer
Interventions Glofitamab will be administered on a step-up dosing schedule, starting on Day 8 of Cycle 3 (2.5 mg), Day 15 of Cycle 3 (10 mg), followed by 30 mg on Day 8 of Cycles 4-6 and Day 1 of Cycles 7-10, with each cycle being 21 days in length…
Registration date Dec 18, 2023
Target size 2
Secondary IDs 2021-001647-28;NCT04980222;NL78443.056.21
Registry page onderzoekmetmensen.nl

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