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A Multicenter Access and Distribution Protocol for Unlicensed Cryopreserved Cord Blood Units (CBUs)
NCT01351545 · View on ClinicalTrials.gov ↗
Study Summary
This study is an access and distribution protocol for unlicensed cryopreserved cord blood units (CBUs) in pediatric and adult patients with hematologic malignancies and other indications.
Conditions Studied
Interventions
- DRUG A multicenter access and distribution protocol for unlicensed cryopreserved cord blood units (CBUs)
Study Locations (20)
California
- City of Hope — Duarte
- Children's Hospital of Los Angeles — Glendale
- Scripps Green Hospital — La Jolla
- University of California San Diego — La Jolla
- Loma Linda University Cancer Center — Loma Linda
- UCLA — Los Angeles
- Children's Hospital and Research Center of Oakland — Oakland
- Children's Hospital of Orange County (CHOC) — Orange
- Sutter Medical Center — Sacramento
- Rady Children's Hospital San Diego — San Diego
- UCSF (adults) — San Francisco
- UCSF (Peds) — San Francisco
- Stanford University Medical Center — Stanford
Arizona
- Banner MD Anderson Cancer Center — Gilbert
- Phoenix Children's Hospital — Phoenix
- Mayo Clinic Arizona (adults) — Phoenix
- University of Arizona Medical Center - Tucson — Tucson
Alabama
- University of Alabama at Birmingham — Birmingham
Arkansas
- Arkansas Children's Hospital — Little Rock
Colorado
- Children's Hospital Colorado — Aurora
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 99,999 participants |
| Start Date | 2011-10 |
| Est. Completion | 2041-10 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT01351545
The ClinicalTrials.gov registry entry for NCT01351545 describes a study currently listed as recruiting. It is categorized as an unspecified phase, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 99,999 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Center for International Blood and Marrow Transplant Research, which has 16 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.
The record links to 10 conditions, with Hematologic Malignancies appearing as the primary indexed condition, and to 1 intervention — of which A multicenter access and distribution protocol for unlicensed cryopreserved cord blood units (CBUs) is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.
Geographic footprint matters for practical reasons: NCT01351545 reports 20 study locations spanning 5 distinct geographic areas — top geographies include California, Arizona, Alabama. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.
Frequently Asked Questions
What is clinical trial NCT01351545 about?
NCT01351545 is a clinical study titled "A Multicenter Access and Distribution Protocol for Unlicensed Cryopreserved Cord Blood Units (CBUs)". This study is an access and distribution protocol for unlicensed cryopreserved cord blood units (CBUs) in pediatric and adult patients with hematologic malignancies and other indications.
What is the current status of trial NCT01351545?
This trial is currently recruiting. The enrollment target is 99,999 participants. The study started on 2011-10. Estimated completion is 2041-10.
What conditions does trial NCT01351545 study?
This clinical trial studies the following conditions: Hematologic Malignancies, Acute Lymphoblastic Leukemia (ALL), Chronic Myelogenous Leukemia (CML), Histiocytic Disorders, Inherited Disorders of Metabolism. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT01351545?
The interventions under investigation include: A multicenter access and distribution protocol for unlicensed cryopreserved cord blood units (CBUs) (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT01351545?
This trial is sponsored by Center for International Blood and Marrow Transplant Research, which has 16 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT01351545 being conducted?
This trial has 20 study locations across Alabama, Arizona, Arkansas, California, Colorado. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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