drugset / Trial / NCT01905943

A Safety and Efficacy Study of Obinutuzumab Alone or in Combination With Chemotherapy in Participants With Chronic Lymphocytic Leukemia

NCT01905943

Phase 3 Completed 979 enrolled Hoffmann-La Roche
NaSingle-groupOpen-labelTreatment

Summary

This multicenter, open-label, single-arm study will evaluate the safety and efficacy of obinutuzumab alone or in combination with chemotherapy in participants with previously untreated or relapsed/refractory chronic lymphocytic leukemia (CLL). This is a Post-Authorization Safety Study. Participants will receive 6 cycles of single-agent obinutuzumab or obinutuzumab in combination with chemotherapy at the investigator's discretion. Each participant will be followed until 30 months after the last participant has been enrolled. Total length of the study is anticipated to be approximately 5 years.

Timeline

Start
2013-11-04
Primary completion
2016-12-29
Completion
2018-10-08

Drugs

EvaluationDrugModalityDoseRoute
Subject Bendamustine Small molecule 50 mg/m2 Intravenous
Subject Bendamustine Small molecule 70 mg/m2 Intravenous
Subject Bendamustine Small molecule 90 mg/m2 Intravenous
Subject Chlorambucil Other / unclassified 0.5 mg/kg Oral
Subject Cyclophosphamide Other / unclassified 250 mg/m2 Intravenous
Subject Fludarabine Small molecule 25 mg/m2 Intravenous
Subject Fludarabine Small molecule 40 mg/m2 Intravenous
Subject Obinutuzumab Monoclonal antibody 1000 mg Intravenous