A Dose Study of Doxil in a Dose Dense, 14 Day CDOP/Rituximab Regimen for Patients With Diffuse Large B-Cell Non-Hodgkin Lymphoma (NHL)> 60 Years or With Compromised Cardiac Status.
Part of paid clinical trials in Baltimore, Maryland.
- Sponsor
- The Alvin and Lois Lapidus Cancer Institute
- Study ID
- NCT00333008
- Phase
- PHASE2
- Status
- Unknown
Conditions
- Diffuse Large B Cell Lymphoma
- Lymphoma, Non-Hodgkin
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- Doxil — DRUG
- Cyclophosphamide — DRUG
- Vincristine — DRUG
- Prednisone — DRUG
- Rituximab — DRUG
- Pegfilgrastim — DRUG
Study Details
The purpose of this study is to evaluate the feasibility and tolerability of delivering a full dose, on time schedule of dose-dense CDOP-R (cyclophosphamide, doxil, vincristine, prednisone, and rituximab) in NHL.
Key Dates
- Start date
- May 31, 2006
- Status verified
- Sep 2006
Study Design
- Enrollment
- 27 participants
- Allocation
- NON_RANDOMIZED
- Intervention model
- PARALLEL
- Primary purpose
- TREATMENT
Primary Outcome Measure
Safety assessment: National Cancer Institute (NCI) Common Terminology Criteria for Adverse Events (CTACAE) v3.0
Central Contacts
- Pam Nickoles, RN, BSN410-601-0729
- Judy Bosley, RN, BSN410-601-4392
Locations (2)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| Sinai Hospital of Baltimore | Baltimore | Maryland | 21215 | Stephen Noga, MD, PhD (PRINCIPAL_INVESTIGATOR) |
| Northwest Hospital Center | Randallstown | Maryland | 21133 | Stephen Noga, MD, PhD (PRINCIPAL_INVESTIGATOR) |
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