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NCT01926899 · ClinicalTrials.gov registry record · Phase 1

A Multicenter Phase I Study Evaluating the Addition of Bortezomib to an Established Acute Graft Versus Host Disease Prophylaxis Regimen in Pediatric Allogeneic Hematopoietic Stem Cell Transplant Patients

A Phase 1 study, sponsored by Indiana University.

Completed
Registry status
Phase 1
Development phase
15
Enrollment target

NCT01926899 is a Phase 1 study that has completed, run by Indiana University. The registered enrollment target is 15 participants.

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The verdict

NCT01926899, a Phase 1 study, has completed, sponsored by Indiana University.

COMPLETED
Registry status
Phase 1
Development phase
15 participants
Enrollment target

Study Summary

The objective of this study is to determine the maximum tolerated dose (MTD) of bortezomib in combination with calcineurin inhibitor and methotrexate as acute graft versus host disease (aGVHD) prophylaxis in pediatric patients undergoing allogeniec hematopoietic stem cell transplant (alloHSCT)

Interventions

  • DRUG Bortezomib administration

Trial Details

FieldValue
Enrollment Target 15 participants
Start Date 2013-08-01
Est. Completion 2018-03-15
Phase Phase 1

Sponsor

Indiana University

890 total trials

What the Registry Record Tells You About NCT01926899

The ClinicalTrials.gov registry entry for NCT01926899 describes a study currently listed as completed, categorized as Phase 1. The registered enrollment target is 15 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Indiana University, which has 890 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 1 intervention - of which Bortezomib administration is the first listed.

NCT01926899 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT01926899 about?

NCT01926899 is a clinical study titled "A Multicenter Phase I Study Evaluating the Addition of Bortezomib to an Established Acute Graft Versus Host Disease Prophylaxis Regimen in Pediatric Allogeneic Hematopoietic Stem Cell Transplant Patients". The objective of this study is to determine the maximum tolerated dose (MTD) of bortezomib in combination with calcineurin inhibitor and methotrexate as acute graft versus host disease (aGVHD) prophylaxis in pediatric patients undergoing allogeniec hematopoietic stem cell transplant (alloHSCT)

What is the current status of trial NCT01926899?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 15 participants. The study started on 2013-08-01. Estimated completion is 2018-03-15.

What interventions are being tested in trial NCT01926899?

The interventions under investigation include: Bortezomib administration (DRUG).

Who is sponsoring clinical trial NCT01926899?

This trial is sponsored by Indiana University, which has 890 total clinical trials registered on ClinicalTrials.gov.

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

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.