drugset / Trial / NCT01332968

A Study of Obinutuzumab (RO5072759) Plus Chemotherapy in Comparison With Rituximab Plus Chemotherapy Followed by Obinutuzumab or Rituximab Maintenance in Patients With Untreated Advanced Indolent Non-Hodgkin's Lymphoma (GALLIUM)

NCT01332968 ↗

RandomizedParallel-groupOpen-labelTreatment

Summary

This open-label, randomized study will assess the efficacy and safety of obinutuzumab (RO5072759) in combination with chemotherapy compared to rituximab (MabThera/Rituxan) with chemotherapy followed by obinutuzumab or rituximab maintenance in participants with untreated advanced indolent non-Hodgkin's lymphoma. After the end of the induction period, participants achieving response (Complete response \[CR\] or partial response \[PR\]) will undergo a maintenance period continuing on the randomized antibody treatment alone every 2 months until disease progression for a total of 2 years. Anticipated time on study treatment is up to approximately 2.5 years. After maintenance or observation, participants will be followed for 5 years until progression. After progression, participants will be followed for new anti-lymphoma therapy and overall survival until the end of the study.

Timeline

Start
2011-07-06
Primary completion
2016-02-01
Completion
2021-07-30

Outcome

Met primary endpoint

registry NUMBER Rituximab+Chemotherapy: 24.0 percentage of participants with event NCT01332968 ↗

registry NUMBER Obinutuzumab+Chemotherapy: 16.8 percentage of participants with event NCT01332968 ↗

registry Rituximab+Chemotherapy vs Obinutuzumab+Chemotherapy; p = 0.0012; Hazard Ratio (HR) 0.66 (95% CI 0.51 to 0.85); Log Rank NCT01332968 ↗

paper obinutuzumab-based chemotherapy resulted in a significantly lower risk of progression, relapse, or death than rituximab-based chemotherapy PMID 28976863 ↗

release “Phase III GALLIUM study met primary endpoint early, as determined by independent data monitoring committee” gene.com ↗

release “GALLIUM study is the first phase III study in previously untreated follicular lymphoma to show superior PFS” roche.com ↗

release “第III相臨床試験であるGALLIUM試験の主要評価項目の早期達成を、独立データモニタリング委員会が決定” nippon-shinyaku.co.jp ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Obinutuzumab Monoclonal antibody 1000 mg Intravenous
Comparator Rituximab Monoclonal antibody 375 mg/m2 Intravenous
Background Bendamustine Small molecule 90 mg/m2 Intravenous
Background Cyclophosphamide Other / unclassified 750 mg/m2 Intravenous
Background Doxorubicin Other / unclassified 50 mg/m2 Intravenous
Background Prednisone Other / unclassified 100 mg Oral
Background Vincristine Small molecule 1.4 mg/m2 Intravenous

Indications