ClinicalTrials.gov record
Completed Phase 1 Interventional

Low-Dose Fludarabine, Busulfan, and Anti-Thymocyte Globulin Followed By Donor Umbilical Cord Blood Transplant in Treating Patients With Advanced Hematologic Cancer

ClinicalTrials.gov ID: NCT00301951

Public ClinicalTrials.gov record NCT00301951. 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 May 6, 2026, 8:52 AM EDT

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

Official title

Pilot Study of Reduced-Intensity Umbilical Cord Blood Transplantation in Adult Patients With Advanced Hematopoietic Malignancies

Study identification

NCT ID
NCT00301951
Recruitment status
Completed
Study type
Interventional
Phase
Phase 1
Lead sponsor
University of California, San Francisco
Other
Enrollment
7 participants

Conditions and interventions

Interventions

  • anti-thymocyte globulin Biological
  • busulfan Drug
  • fludarabine phosphate Drug
  • mycophenolate mofetil Drug
  • sargramostim Biological
  • tacrolimus Drug
  • umbilical cord blood transplantation Procedure

Biological · Drug · Procedure

Eligibility (public fields only)

Age range
18 Years to 70 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
Aug 31, 2004
Primary completion
Jun 30, 2009
Completion
Jun 30, 2009
Last update posted
Oct 11, 2017

2004 – 2009

United States locations

U.S. sites
1
U.S. states
1
U.S. cities
1
Facility City State ZIP Site status
UCSF Comprehensive Cancer Center San Francisco California 94143-0324

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 NCT00301951, 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 Oct 11, 2017 · Synced May 6, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00301951 live on ClinicalTrials.gov.

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