Study of the Efficacy and Safety of Ublituximab in Patients With Relapsed or Refractory B-cell No… (NCT01647971) | Clinical Trial Compass
CompletedPhase 1/2
Study of the Efficacy and Safety of Ublituximab in Patients With Relapsed or Refractory B-cell Non-Hodgkin Lymphoma
United States39 participantsStarted 2012-07-19
Plain-language summary
The purpose of this study is to determine whether ublituximab is safe and effective in patients with relapsed or refractory B-cell lymphoma who were previously treated with rituximab.
Who can participate
Age range18 Years
SexALL
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Inclusion Criteria:
* Relapsed or Refractory B-cell Lymphoma
* Measurable or Evaluable Disease
* Previously treated with at least one line of rituximab or a rituximab based therapy
* Patients ineligible for high dose or combination chemotherapy + stem cell transplant
* Eastern Cooperative Oncology Group (ECOG) Performance Status of 0, 1 or 2
* No active or chronic infection of Hepatitis B or C and no history of HIV based on negative serology
Exclusion Criteria:
* Prior chemotherapy, investigational therapy or radiotherapy within 3 weeks of study entry
* Prior autologous or allogeneic stem cell transplantation within 3 months of study entry
* History of severe hypersensitivity or anaphylaxis to prior rituximab
* Uncontrolled inter-current illness including, but not limited to, ongoing or active infection, symptomatic congestive heart failure, unstable angina pectoris, cardiac arrhythmia, brain metastasis, or psychiatric illness that would limit compliance with study requirements
* Pregnant women
What they're measuring
1
Number of Participants with Adverse Events as a Measure of Safety and Tolerability
Timeframe: Subjects will be followed for 4 weeks
2
Maximum Tolerated Dose acceptable for participants