Study of GS-0189 (Formerly FSI-189) as Monotherapy and in Combination With Rituximab in Participants With Relapsed/Refractory Non-Hodgkin Lymphoma
Stopped early · Phase 1
Conditions studied: Non-hodgkin Lymphoma
In brief
The primary objective of this study is to determine the safety and tolerability of GS-0189 (formerly FSI-189) as monotherapy and in combination with rituximab in participants with relapsed/refractory (R/R) non-Hodgkin lymphoma (NHL).
Key facts
- Study ID
- NCT04502706
- Run by
- Gilead Sciences
- People needed
- 9
- Starts
- 2020-11-17
- Expected to finish
- 2022-03-31
- Last updated by the study team
- 2023-06-05
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
Where it is running
- University of Alabama Comprehensive Cancer Center — Birmingham, Alabama, United States
- City of Hope — Duarte, California, United States
- Florida Cancer Specialists — Sarasota, Florida, United States
- Washington University School of Medicine — St Louis, Missouri, United States
- University of Oklahoma Health Sciences Center — Oklahoma City, Oklahoma, United States
Full record on ClinicalTrials.gov
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