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NCT01652092 · ClinicalTrials.gov registry record · NA

Allogeneic Hematopoietic Stem Cell Transplant for Patients With Primary Immune Deficiencies

A NA study of Chronic Granulomatous Disease and Common Variable Immunodeficiency, sponsored by Masonic Cancer Center, University of Minnesota.

Active
Registry status
NA
Development phase
57
Enrollment target
1
Study location

NCT01652092 is a NA study of Chronic Granulomatous Disease and Common Variable Immunodeficiency that is active but no longer recruiting, run by Masonic Cancer Center, University of Minnesota. The registered enrollment target is 57 participants, above the 27-participant average among 10 other Chronic Granulomatous Disease trials with a reported enrollment target (111% higher). The trial reports 1 study location across 1 state.

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The verdict

NCT01652092, a NA study of Chronic Granulomatous Disease and Common Variable Immunodeficiency, is active but no longer recruiting, sponsored by Masonic Cancer Center, University of Minnesota.

ACTIVE NOT RECRUITING
Registry status
NA
Development phase
57 participants
Enrollment target
1
Study location

Study Summary

This is a standard of care treatment guideline for allogeneic hematopoetic stem cell transplant (HSCT) in patients with primary immune deficiencies.

Interventions

  • DRUG Cyclophosphamide
  • DRUG Busulfan
  • DRUG Alemtuzumab 0.3 mg
  • BIOLOGICAL Stem Cell Transplantation
  • DRUG Fludarabine phosphate 40 mg

Study Locations (1)

Minnesota

  • Masonic Cancer Center, University of Minnesota - Minneapolis

Trial Details

FieldValue
Enrollment Target 57 participants
Start Date 2012-09-04
Est. Completion 2026-12
Phase NA

What the Registry Record Tells You About NCT01652092

The ClinicalTrials.gov registry entry for NCT01652092 describes a study currently listed as active not recruiting, categorized as NA. The registered enrollment target is 57 participants, a figure that helps gauge the scale of data the investigators plan to collect, above the 27-participant average among 10 other Chronic Granulomatous Disease trials with a reported enrollment target (111% higher). The listed sponsor is Masonic Cancer Center, University of Minnesota, which has 249 total studies on file at ClinicalTrials.gov.

The record links to 10 conditions, with Chronic Granulomatous Disease appearing as the primary indexed condition, and to 5 interventions - of which Cyclophosphamide is the first listed.

NCT01652092 reports 1 study location spanning 1 distinct geographic area - top geographies include Minnesota.

Frequently Asked Questions

What is clinical trial NCT01652092 about?

NCT01652092 is a clinical study titled "Allogeneic Hematopoietic Stem Cell Transplant for Patients With Primary Immune Deficiencies". This is a standard of care treatment guideline for allogeneic hematopoetic stem cell transplant (HSCT) in patients with primary immune deficiencies.

What is the current status of trial NCT01652092?

This trial is currently active not recruiting. It is a NA study. The enrollment target is 57 participants. The study started on 2012-09-04. Estimated completion is 2026-12.

What conditions does trial NCT01652092 study?

This clinical trial studies the following conditions: Chronic Granulomatous Disease, Common Variable Immunodeficiency, Wiskott-Aldrich Syndrome, SCI/D, CD40 Ligand Deficiency.

What interventions are being tested in trial NCT01652092?

The interventions under investigation include: Cyclophosphamide (DRUG), Busulfan (DRUG), Alemtuzumab 0.3 mg (DRUG), Stem Cell Transplantation (BIOLOGICAL), Fludarabine phosphate 40 mg (DRUG).

Who is sponsoring clinical trial NCT01652092?

This trial is sponsored by Masonic Cancer Center, University of Minnesota, which has 249 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT01652092 being conducted?

This trial has 1 study location across Minnesota. 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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