drugset / Trial / NCT02966730
Ibrutinib for Patients With Follicular Lymphoma Without Complete Response to Initial Chemoimmunotherapy
Phase 0
Terminated
2 enrolled
Memorial Sloan Kettering Cancer Center
Fox Chase Cancer Center · collabPharmacyclics LLC. · collab
NaSingle-groupOpen-labelTreatment
Summary
The purpose of this study is to find out how successful ibrutinib is at putting follicular lymphoma into full remission. In this study, remission will be determined by achieving a normal PET scan after treatment. A PET scan is an imaging test that looks for active lymphoma. People who don't have a complete remission on PET after their first treatment are at high risk for having their lymphoma return. This study will investigate if ibrutinib will help participants achieve a complete remission without giving additional chemotherapy. The study will also investigate any possible side effects of the study drug ibrutinib.
Timeline
- Start
- 2016-11
- Primary completion
- 2019-06-20
- Completion
- 2019-06-20
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Ibrutinib | Small molecule | 560 mg | Oral |