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High Dose Chemotherapy and Allogeneic Hematopoietic Cell Transplant for Non-Hodgkin's Lymphoma

High Dose Chemotherapy and Allogeneic Hematopoietic Cell Transplantation for Non-Hodgkin's Lymphoma

Status
Completed
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00186394
Enrollment
35
Registered
2005-09-16
Start date
2000-04-30
Completion date
2006-12-31
Last updated
2010-07-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Blood and Marrow Transplant (BMT), Lymphoma, Non-Hodgkin, Lymphomas: Non-Hodgkin

Brief summary

To evaluate the role of allogeneic hematopoietic cell transplantation in the treatment of NHL.

Detailed description

To determine safety and toxicity of a regimen of high dose chemotherapy with allogeneic peripheral blood progenitor cell transplantation; determine the efficacy of the procedure by following clinical outcomes and quality of life measures; and evaluate graft versus host disease incidence and severity with regimen.

Interventions

Sponsors

National Institutes of Health (NIH)
CollaboratorNIH
Stanford University
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 61 Years
Healthy volunteers
No

Inclusion criteria

Morphologically confirmed relapsed non-Hodgkin's lymphoma Age: \>18 and \<61 years of age Signed informed consent

Exclusion criteria

Hepatic dysfunction defined by serum transaminases \>2.5X normal values Serum creatinine of \> 2 mg/dl or creatinine clearance \< 60 ml/min Diseases other than non-Hodgkin's lymphoma Prior bone marrow transplant procedure Severe psychological or medical illness

Design outcomes

Primary

MeasureTime frame
Safety
Toxicity
Efficacy

Secondary

MeasureTime frame
Incidence of acute and chronic GVHD

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026