Study of High-Dose Rituximab With Temozolomide as Treatment for Primary Central Nervous System (CNS) Lymphoma
Part of paid clinical trials in New Haven, Connecticut.
- Sponsor
- SCRI Development Innovations, LLC
- Study ID
- NCT02113007
- Phase
- PHASE2
- Status
- Terminated
Conditions
- Primary Central Nervous System Lymphoma
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- Rituximab plus Temozolomide — DRUGTreatment cycles will be repeated every 14 days (2 weeks) for the lead-in portion. If no prohibitive toxicities are observed in the first 6 patients during the first 2 treatment cycles, the study will continue enrolling patients. Treatment cycles for the Phase II portion will be repeated every 14 days (2 weeks) for a total of 12 cycles.
Study Details
This study will evaluate the safety and efficacy of high-dose rituximab combined with temozolomide in the treatment of patients with Primary Central Nervous System Lymphomas (PCNSL). This novel combination will be evaluated in PCNSL patients who are 60 years of age or older, or in patients 18 years or older who refuse methotrexate-based treatment.
Key Dates
- Start date
- Jul 31, 2014
- Status verified
- Dec 2016
- Primary completion
- Feb 29, 2016
- Completion
- Feb 29, 2016
Study Design
- Enrollment
- 2 participants (actual)
- Allocation
- NA
- Intervention model
- SINGLE_GROUP
- Primary purpose
- TREATMENT
Arms
- Experimental: Rituximab plus TemozolomideRituximab: 375 mg/m2 IV, days 1, 3, and 5 Temozolomide: 150 mg/m2 PO, days 1-5
Primary Outcome Measure
Overall Response Rate [ Time Frame: approximately 32 weeks ]
Locations (4)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| Yale School of Medicine | New Haven | Connecticut | 06520 | - |
| Memorial Cancer Institute | Hollywood | Florida | 33021 | - |
| Florida Hospital Cancer Institute | Orlando | Florida | 32804 | - |
| Tennessee Oncology PLLC | Nashville | Tennessee | 37203 | - |
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