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Completed Phase 2 Interventional

Fludarabine and Cyclophosphamide Followed by Peripheral Stem Cell Transplant in Treating Patients With Leukemia or Lymphoma

ClinicalTrials.gov ID: NCT00006252

Public ClinicalTrials.gov record NCT00006252. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 30, 2026, 4:01 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

Minimal Ablation and Cellular Immune Therapy of Chronic Lymphocytic Leukemia, Prolymphocytic Leukemia, Low-Grade Non-Hodgkin's Lymphoma, and Mantle Cell Lymphoma With Allogeneic Donor Stem Cells

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

RATIONALE: Giving chemotherapy drugs, such as fludarabine and cyclophosphamide, before a donor peripheral blood stem cell transplant helps stop the growth of cancer cells. It also helps stop the patient's immune system from rejecting the donor's stem cells. When the healthy stem cells from a donor are infused into the patient they may help the patient's bone marrow make stem cells, red blood cells, white blood cells, and platelets. PURPOSE: This phase II trial is studying how well fludarabine and cyclophosphamide followed by peripheral stem cell transplant works in treating patients with leukemia or lymphoma.

Study identification

NCT ID
NCT00006252
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Cancer and Leukemia Group B
Network
Enrollment
47 participants

Conditions and interventions

Interventions

Drug · Biological

Eligibility (public fields only)

Age range
Up to 69 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Feb 2001 (Type not available)
Primary completion
Jan 2007 (Actual)
Completion
Oct 2011 (Actual)
Last update posted
Jul 18, 2016

2001 – 2011

United States locations

U.S. sites
19
U.S. states
11
U.S. cities
19
Facility City State ZIP Site status
Rebecca and John Moores UCSD Cancer Center La Jolla California 92093-0658 —
Veterans Affairs Medical Center - San Diego San Diego California 92161 —
UCSF Comprehensive Cancer Center San Francisco California 94115 —
Beebe Medical Center Lewes Delaware 19958 —
CCOP - Christiana Care Health Services Newark Delaware 19713 —
St. Francis Hospital Wilmington Delaware 19805 —
Holden Comprehensive Cancer Center at University of Iowa Iowa City Iowa 52242 —
Union Hospital Cancer Center at Union Hospital Elkton MD Maryland 21921 —
UMASS Memorial Cancer Center - University Campus Worcester Massachusetts 01655 —
Cancer Institute of New Jersey at the Cooper University Hospital - Voorhees Voorhees Township New Jersey 08043 —
Roswell Park Cancer Institute Buffalo New York 14263-0001 —
Elmhurst Hospital Center Elmhurst New York 11373 —
Queens Cancer Center of Queens Hospital Jamaica New York 11432 —
Mount Sinai Medical Center New York New York 10029 —
Lineberger Comprehensive Cancer Center at University of North Carolina - Chapel Hill Chapel Hill North Carolina 27599-7295 —
Wake Forest University Comprehensive Cancer Center Winston-Salem North Carolina 27157-1096 —
Arthur G. James Cancer Hospital and Solove Research Institute at Ohio State University Columbus Ohio 43210-1240 —
Western Pennsylvania Cancer Institute at Western Pennsylvania Hospital Pittsburgh Pennsylvania 15224-1791 —
Massey Cancer Center at Virginia Commonwealth University Richmond Virginia 23298-0037 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00006252, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jul 18, 2016 · Synced Oct 30, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00006252 live on ClinicalTrials.gov.

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