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NCT03128996 · ClinicalTrials.gov registry record · Phase 1

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

A Phase 1 study of Hemoglobinopathies and Metabolic Disorders, sponsored by Washington University School of Medicine.

Recruiting
Registry status
Phase 1
Development phase
29
Enrollment target
4
Study locations

NCT03128996 is a Phase 1 study of Hemoglobinopathies and Metabolic Disorders that is actively recruiting participants, run by Washington University School of Medicine. The registered enrollment target is 29 participants, below the 1,802-participant average among 17 other Hemoglobinopathies trials with a reported enrollment target (98% lower). The trial reports 4 study locations across 4 states.

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The verdict

NCT03128996, a Phase 1 study of Hemoglobinopathies and Metabolic Disorders, is actively recruiting participants, sponsored by Washington University School of Medicine.

RECRUITING
Registry status
Phase 1
Development phase
29 participants
Enrollment target
4
Study locations

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

What the Registry Record Tells You About NCT03128996

The ClinicalTrials.gov registry entry for NCT03128996 describes a study currently listed as recruiting, categorized as Phase 1. The registered enrollment target is 29 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 1,802-participant average among 17 other Hemoglobinopathies trials with a reported enrollment target (98% lower). The listed sponsor is Washington University School of Medicine, which has 1,502 total studies on file at ClinicalTrials.gov.

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.

NCT03128996 reports 4 study locations spanning 4 distinct geographic areas - top geographies include Connecticut, Delaware, Michigan.

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.

What interventions are being tested in trial NCT03128996?

The interventions under investigation include: RIC regimen (DRUG), GVHD prophylaxis regimen (DRUG).

Who is sponsoring clinical trial NCT03128996?

This trial is sponsored by Washington University School of Medicine, which has 1,502 total clinical trials registered on ClinicalTrials.gov.

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.

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

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