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NCT00708721 · ClinicalTrials.gov registry record · Phase 1

Low-dose Oral Clofarabine for the Treatment of IPSS INT-1, INT-2 or HIGH Myelodysplastic Syndromes and Chronic Myelomonocytic Leukemia

A Phase 1 study, sponsored by University of Utah.

Terminated
Registry status
Phase 1
Development phase
11
Enrollment target

NCT00708721 is a Phase 1 study that was terminated before completion, run by University of Utah. The registered enrollment target is 11 participants.

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The verdict

NCT00708721, a Phase 1 study, was terminated before completion, sponsored by University of Utah.

TERMINATED
Registry status
Phase 1
Development phase
11 participants
Enrollment target

Study Summary

Study and Dose Rationale The safety profile of clofarabine appears acceptable within the target populations studied to date in the clinical studies summarized in Section 2.3. clofarabine has demonstrated anti-cancer activity through inhibition of DNA synthesis and repair, induction of apoptosis, and possibly through other mechanisms. The effect of clofarabine on DNA methylation has not been determined. Numerous responses have been observed after treatment with clofarabine in heavily pre-treated relapsed/refractory patients with ALL or AML. Recently 2 small studies were conducted at the M.D. Anderson Cancer Center looking at the use of clofarabine in the treatment of MDS.31 The first study randomized patients in a Bayesian fashion to 15 vs. 30 mg/m2 given IV daily for 5 days every 4 to 8 weeks. In the 15 mg/m2 arm 3 of 7 patients had a complete remission according to the International Working Group (IWG)32 criteria for response. In the 30 mg/m2 arm, 2 of 6 patients had a complete remission while 1 patient had hematologic improvement according to IWG criteria. In the second study, patients were treated with oral clofarabine at a dose of 40 mg/m2 daily for 5 days every 4 to 8 weeks. Two of 7 patients had hematologic improvement according to IWG criteria. The main toxicities in both trials were prolonged myelosuppression and liver function abnormalities. Preclinical animal models have shown increased clofarabine activity against multiple different tumors with repetitive daily dosing for prolonged periods of time.33 The use of an oral therapy is advantageous for the treatment of a chronic malignancy such as MDS. Furthermore, based on the pre-clinical data mentioned above daily repetitive dosing over a protracted period may provide increased efficacy. Since most MDS patients are elderly and may not tolerate aggressive therapy, a schedule of administration of low dose oral clofarabine over a protracted period may provide the advantage of increased efficacy without severe

Interventions

  • DRUG Clofarabine

Trial Details

FieldValue
Enrollment Target 11 participants
Start Date 2008-03
Est. Completion 2014-11
Phase Phase 1

Sponsor

University of Utah

818 total trials

What the Registry Record Tells You About NCT00708721

The ClinicalTrials.gov registry entry for NCT00708721 describes a study currently listed as terminated, categorized as Phase 1. The registered enrollment target is 11 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is University of Utah, which has 818 total studies on file at ClinicalTrials.gov.

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

NCT00708721 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT00708721 about?

NCT00708721 is a clinical study titled "Low-dose Oral Clofarabine for the Treatment of IPSS INT-1, INT-2 or HIGH Myelodysplastic Syndromes and Chronic Myelomonocytic Leukemia". Study and Dose Rationale The safety profile of clofarabine appears acceptable within the target populations studied to date in the clinical studies summarized in Section 2.3. clofarabine has demonstrated anti-cancer activity through inhibition of DNA synthesis and repair, induction of apoptosis, and...

What is the current status of trial NCT00708721?

This trial is currently terminated. It is a Phase 1 study. The enrollment target is 11 participants. The study started on 2008-03. Estimated completion is 2014-11.

What interventions are being tested in trial NCT00708721?

The interventions under investigation include: Clofarabine (DRUG).

Who is sponsoring clinical trial NCT00708721?

This trial is sponsored by University of Utah, which has 818 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.