Study Evaluating TRU-015 in B-Cell Non-Hodgkin's Lymphoma
Stopped early · Phase 1
Conditions studied: Lymphoma, B-Cell
In brief
This is a study to evaluate the safety and efficacy of TRU-015 in treatment of B-cell Non-Hodgkin's Lymphoma (NHL). TRU-015 is also currently being evaluated in multiple clinical studies for the treatment of autoimmune disorders. Over 300 patients have received TRU-015 in these studies, and the data observed to date support its safety in patients with autoimmune disorders. Safety of an escalating dose of 4 weekly infusions of TRU-015 will be evaluated in subjects with relapsed NHL (see inclusion criteria for subtypes). Once a maximum tolerated dose (MTD) is confirmed or maximum dose to be studied is determined to be safe and well tolerated, an expanded cohort of subjects with relapsed follicular NHL will be evaluated for efficacy.
Key facts
- Study ID
- NCT00521638
- Run by
- Wyeth is now a wholly owned subsidiary of Pfizer
- People needed
- 120
- Starts
- 2007-09-01
- Expected to finish
- 2008-04-01
- Last updated by the study team
- 2021-02-18
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
Where it is running
- Study site — Duarte, California, United States
- Study site — San Diego, California, United States
- Study site — Chicago, Illinois, United States
- Study site — Boston, Massachusetts, United States
- Study site — St Louis, Missouri, United States
- Study site — Buffalo, New York, United States
- Study site — Cleveland, Ohio, United States
Full record on ClinicalTrials.gov
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