Safety and Efficacy of Campath in Nonmyeloablative Transplantation
Part of paid clinical trials in Houston, Texas.
- Sponsor
- M.D. Anderson Cancer Center
- Study ID
- NCT00038844
- Status
- Completed
Conditions
Eligibility Criteria
- Sex
- ALL
- Age
- N/A - 70 Years
- Healthy Volunteers
- Not accepted
Interventions
- Campath-1 H (Alemtuzumab) — DRUGStarting Dose of 15 mg by vein daily, 3 days in a row.
- Fludarabine — DRUG30 mg/m2 by vein daily, 3 days in a row.
- Cyclophosphamide — DRUG1 gm/m2 by vein daily, 3 days in a row.
- Rituximab — DRUG375 mg/m2 by vein, given (to some patients only, based on the subtypes of lymphomas) eight days before the transplant and then weekly for a total of 4 doses.
Study Details
Objective of the low-dose transplant regimen must produce the following effects: 1. Suppression of the patient's immune system to prevent rejection of the donor cells; 2. Control of the lymphoma. The pretransplant regimen must suppress the lymphoma sufficiently to prevent marked progression of the tumor and allow time for the GVT effect to occur.
Key Dates
- Start date
- Jun 30, 2001
- Status verified
- Oct 2011
- Primary completion
- Dec 31, 2007
- Completion
- Sep 30, 2010
Study Design
- Enrollment
- 65 participants (actual)
- Allocation
- NON_RANDOMIZED
- Intervention model
- SINGLE_GROUP
- Primary purpose
- TREATMENT
Arms
- Experimental: Campath in Nonmyeloablative TransplantationCampath-1 H Starting Dose of 15 mg by vein daily, 3 days in a row + Fludarabine 30 mg/m2 by vein daily, 3 days in a row + Cyclophosphamide 1 gm/m2 by vein daily, 3 days in a row + Rituximab 375 mg/m2 by vein, given 8 days before transplant then weekly for 4 total doses.
Primary Outcome Measure
Number of Participants Surviving 100 days post-transplant [ Time Frame: 30 Day Engraftment (Baseline) to 100 Days post-transplant ]
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| U.T.M.D. Anderson Cancer Center | Houston | Texas | 77030 | - |
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