drugset / Trial / NCT02689869
Combination of PCI-32765 With Obinutuzumab in Untreated Follicular Lymphoma
Phase 2
Unknown
98 enrolled
Ludwig-Maximilians - University of Munich
Hoffmann-La Roche · collabJanssen-Cilag G.m.b.H · collab
NaSingle-groupOpen-labelTreatment
Summary
Primary Objectives The primary objective of this study is to evaluate the efficacy of the chemotherapy-free combination of ibrutinib and obinutuzumab (GA 101) in patients with previously untreated follicular lymphoma (FL) and a high tumor burden. Primary endpoint to be observed for this is the rate of progression free survival one year after start of therapy. Hypothesis The hypothesis of the study is that ibrutinib in combination with obinutuzumab will achieve response rates (CR and PR), rates of MRD negativity and PFS which are comparable to currently used standard rituximab-chemotherapy combinations such as R-CHOP or R-bendamustine in subjects with previously untreated FL and a high tumor burden.
Timeline
- Start
- 2016-04
- Primary completion
- 2022-04
- Completion
- 2022-07
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Ibrutinib | Small molecule | 560 mg | Oral |
| Subject | Obinutuzumab | Monoclonal antibody | 1000 mg | Intravenous |