VELCADE® Plus Rituximab in Non Hodgkin's Follicular Lymphoma
- Sponsor
- Gruppo Italiano Studio Linfomi
- Study ID
- NCT01830465
- Phase
- PHASE2
- Status
- Completed
Conditions
- Non Hodgkin's Follicular Lymphoma
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - 90 Years
- Healthy Volunteers
- Not accepted
Interventions
- Bortezomib (VELCADE) — DRUG1,3 mg/m2, intravenous bolus (over 3-5 seconds) on days 1, 4, 8, 11 of each 21 day cycle. Number of Cycles: 6.
- Rituximab — DRUG375 mg/m2 as intravenous infusion on day 1 of cycle III, IV, V, VI. Two additional doses will be administered at week + 3 and week + 6 after cycle VI.
Study Details
The aim of this study was to evaluate the efficacy and safety of the combination of Velcade and Rituximab in patients with relapsed Non Hodgkin's Follicular Lymphoma.
Key Dates
- Start date
- Aug 31, 2006
- Status verified
- Apr 2013
- Primary completion
- Aug 31, 2008
- Completion
- May 31, 2011
Study Design
- Enrollment
- 45 participants (actual)
- Allocation
- NA
- Intervention model
- SINGLE_GROUP
- Primary purpose
- TREATMENT
Arms
- Experimental: Bortezomib + RituximabSingle arm. Patients will be treated with Bortezomib, 1,3 mg/m2 intravenous bolus (over 3-5 seconds) on days 1, 4, 8, 11 of 21 day cycle for 6 cycles and Rituximab 375 mg/m2 intravenous infusion on day 1 of cycle III, IV, V, VI. Two additional doses will be administered at week + 3 and week + 6 after cycle VI.
Primary Outcome Measure
Antitumor activity after complete treatment [ Time Frame: 30 days after the last infusion of rituximab ]