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NCT01273766 · ClinicalTrials.gov registry record · Phase 2

Deferasirox in Treating Iron Overload Caused By Blood Transfusions in Patients With Hematologic Malignancies

A Phase 2 study, sponsored by Wake Forest University Health Sciences.

Completed
Registry status
Phase 2
Development phase
16
Enrollment target

NCT01273766 is a Phase 2 study that has completed, run by Wake Forest University Health Sciences. The registered enrollment target is 16 participants.

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The verdict

NCT01273766, a Phase 2 study, has completed, sponsored by Wake Forest University Health Sciences.

COMPLETED
Registry status
Phase 2
Development phase
16 participants
Enrollment target

Study Summary

RATIONALE: Deferasirox may remove excess iron from the body caused by blood transfusions. PURPOSE: This clinical trial studies deferasirox in treating iron overload caused by blood transfusions in patients with hematologic malignancies.

Interventions

  • OTHER laboratory biomarker analysis
  • OTHER enzyme-linked immunosorbent assay
  • DRUG deferasirox

Trial Details

FieldValue
Enrollment Target 16 participants
Start Date 2011-01
Est. Completion 2014-12
Phase Phase 2

Sponsor

Wake Forest University Health Sciences

1,140 total trials

What the Registry Record Tells You About NCT01273766

The ClinicalTrials.gov registry entry for NCT01273766 describes a study currently listed as completed, categorized as Phase 2. The registered enrollment target is 16 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Wake Forest University Health Sciences, which has 1,140 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 3 interventions - of which laboratory biomarker analysis is the first listed.

NCT01273766 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT01273766 about?

NCT01273766 is a clinical study titled "Deferasirox in Treating Iron Overload Caused By Blood Transfusions in Patients With Hematologic Malignancies". RATIONALE: Deferasirox may remove excess iron from the body caused by blood transfusions. PURPOSE: This clinical trial studies deferasirox in treating iron overload caused by blood transfusions in patients with hematologic malignancies.

What is the current status of trial NCT01273766?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 16 participants. The study started on 2011-01. Estimated completion is 2014-12.

What interventions are being tested in trial NCT01273766?

The interventions under investigation include: laboratory biomarker analysis (OTHER), enzyme-linked immunosorbent assay (OTHER), deferasirox (DRUG).

Who is sponsoring clinical trial NCT01273766?

This trial is sponsored by Wake Forest University Health Sciences, which has 1,140 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.