An Observational Study on the Safety Profile of MabThera/Rituxan (Rituximab) in Combination With Chemotherapy in Patients With B Cell-lineage Chronic Lymphocytic Leukaemia (MABERYC)
- Sponsor
- Hoffmann-La Roche
- Study ID
- NCT01224093
- Status
- Completed
Conditions
- Lymphocytic Leukemia, Chronic
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- Chemotherapy — DRUGas prescribed
- rituximab [MabThera/Rituxan] — DRUGas prescribed
Study Details
This prospective observational study will evaluate the safety of MabThera/Rituxan (rituximab) in combination with chemotherapy in patients with previously untreated or relapsed/refractory B cell-lineage chronic lymphocytic leukaemia. Data will be collected from each patient for 6-12 months, depending on the prescribed chemotherapy regimen.
Key Dates
- Start date
- Oct 31, 2010
- Status verified
- Nov 2016
- Primary completion
- Feb 28, 2014
- Completion
- Feb 28, 2014
Study Design
- Enrollment
- 219 participants (actual)
Arms
- Arm: First line
- Arm: Relapsed/refractory
Primary Outcome Measure
Safety profile of MabThera/Rituxan in combination with chemotherapy in unselected CLL patients [ Time Frame: 3 years ]
Related Studies
- CAP-100 for Subjects With Relapsed/Refractory Chronic Lymphocytic LeukemiaPHASE1 · Recruiting · Catapult Therapeutics · Boston, Massachusetts