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NCT01174940 · ClinicalTrials.gov registry record · Early Phase 1

Test Extracorporeal Photopheresis (ECP) Treatment Before/After Allogeneic Bone Marrow Transplant (BMT) or Peripheral Blood Stem Cell (PBSC) Transplant to Prevent Graft Versus Host Disease

A Early Phase 1 study, sponsored by University of Kansas Medical Center.

Completed
Registry status
Early Phase 1
Development phase
22
Enrollment target

NCT01174940 is a Early Phase 1 study that has completed, run by University of Kansas Medical Center. The registered enrollment target is 22 participants.

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The verdict

NCT01174940, a Early Phase 1 study, has completed, sponsored by University of Kansas Medical Center.

COMPLETED
Registry status
Early Phase 1
Development phase
22 participants
Enrollment target

Study Summary

To study the effect of ECP with Uvadex® in conjunction with a standard myeloablative conditioning regimen on the incidence of acute and chronic GvHD in patients undergoing an allogeneic related or unrelated BMT or PBSC transplant, for treatment of hematologic or lymphoproliferative malignancies.

Interventions

  • DRUG extracorporeal photopheresis

Trial Details

FieldValue
Enrollment Target 22 participants
Start Date 2010-06
Est. Completion 2015-08
Phase Early Phase 1

Sponsor

University of Kansas Medical Center

408 total trials

What the Registry Record Tells You About NCT01174940

The ClinicalTrials.gov registry entry for NCT01174940 describes a study currently listed as completed, categorized as Early Phase 1. The registered enrollment target is 22 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is University of Kansas Medical Center, which has 408 total studies on file at ClinicalTrials.gov.

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

NCT01174940 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT01174940 about?

NCT01174940 is a clinical study titled "Test Extracorporeal Photopheresis (ECP) Treatment Before/After Allogeneic Bone Marrow Transplant (BMT) or Peripheral Blood Stem Cell (PBSC) Transplant to Prevent Graft Versus Host Disease". To study the effect of ECP with Uvadex® in conjunction with a standard myeloablative conditioning regimen on the incidence of acute and chronic GvHD in patients undergoing an allogeneic related or unrelated BMT or PBSC transplant, for treatment of hematologic or lymphoproliferative malignancies.

What is the current status of trial NCT01174940?

This trial is currently completed. It is a Early Phase 1 study. The enrollment target is 22 participants. The study started on 2010-06. Estimated completion is 2015-08.

What interventions are being tested in trial NCT01174940?

The interventions under investigation include: extracorporeal photopheresis (DRUG).

Who is sponsoring clinical trial NCT01174940?

This trial is sponsored by University of Kansas Medical Center, which has 408 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.