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RECRUITING Phase 1

Reduced Intensity Conditioning and Familial HLA-Mismatched BMT for Non-Malignant Disorders

NCT03128996 · View on ClinicalTrials.gov ↗

Study Summary

This study is designed to estimate the efficacy and toxicity of familial HLA mismatched bone marrow transplants in patients with non-malignant disease who are less than 21 years of age and could benefit from the procedure.

Interventions

  • DRUG RIC regimen
  • DRUG GVHD prophylaxis regimen

Study Locations (4)

Connecticut

  • Yale School of Medicine — New Haven

Delaware

  • Nemours Children's Health — Wilmington

Michigan

  • Helen DeVos Children's Hospital — Grand Rapids

Missouri

  • Washington University School of Medicine — St Louis

Trial Details

FieldValue
Enrollment Target 29 participants
Start Date 2017-03-20
Est. Completion 2033-04
Phase Phase 1

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT03128996

The ClinicalTrials.gov registry entry for NCT03128996 describes a study currently listed as recruiting. It is categorized as Phase 1, 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 29 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Washington University School of Medicine, which has 1,036 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 6 conditions, with Hemoglobinopathies appearing as the primary indexed condition, and to 2 interventions — of which RIC regimen 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: NCT03128996 reports 4 study locations spanning 4 distinct geographic areas — top geographies include Connecticut, Delaware, Michigan. 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 NCT03128996 about?

NCT03128996 is a clinical study titled "Reduced Intensity Conditioning and Familial HLA-Mismatched BMT for Non-Malignant Disorders". This study is designed to estimate the efficacy and toxicity of familial HLA mismatched bone marrow transplants in patients with non-malignant disease who are less than 21 years of age and could benefit from the procedure.

What is the current status of trial NCT03128996?

This trial is currently recruiting. It is a Phase 1 study. The enrollment target is 29 participants. The study started on 2017-03-20. Estimated completion is 2033-04.

What conditions does trial NCT03128996 study?

This clinical trial studies the following conditions: Hemoglobinopathies, Metabolic Disorders, Bone Marrow Failure Syndromes, Non-malignant Disorders, Severe Sickle Cell Disease. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT03128996?

The interventions under investigation include: RIC regimen (DRUG), GVHD prophylaxis regimen (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT03128996?

This trial is sponsored by Washington University School of Medicine, which has 1,036 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT03128996 being conducted?

This trial has 4 study locations across Connecticut, Delaware, Michigan, Missouri. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial