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COMPLETED Phase 2

A Study of 5-Azacitidine (Vidaza®) in Patients With Chronic Myelomonocytic Leukemia

NCT01350947 · View on ClinicalTrials.gov ↗

Study Summary

The primary objective of this study is: Response to treatment will be evaluated according to the revised International Working Group (IWG) categories natural history, hematologic improvement and cytogenetic response1;2. The primary objective is: To determine the rate of complete hematologic response and hematologic improvement (according to IWG 2006 criteria) in CMML patients treated with 5-azacitidine.

Interventions

  • DRUG 5-Azacitidine

Study Locations (3)

New York

  • Roswell Park Cancer Institute — Buffalo

Oregon

  • Oregon Health and Science University — Portland

Utah

  • University of Utah — Salt Lake City

Trial Details

FieldValue
Enrollment Target 11 participants
Start Date 2011-04
Est. Completion 2014-09
Phase Phase 2

Sponsor

University of Utah

686 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT01350947

The ClinicalTrials.gov registry entry for NCT01350947 describes a study currently listed as completed. It is categorized as Phase 2, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. 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 686 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 1 condition, with Chronic Myelomonocytic Leukemia appearing as the primary indexed condition, and to 1 intervention — of which 5-Azacitidine is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT01350947 reports 3 study locations spanning 3 distinct geographic areas — top geographies include New York, Oregon, Utah. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT01350947 about?

NCT01350947 is a clinical study titled "A Study of 5-Azacitidine (Vidaza®) in Patients With Chronic Myelomonocytic Leukemia". The primary objective of this study is: Response to treatment will be evaluated according to the revised International Working Group (IWG) categories natural history, hematologic improvement and cytogenetic response1;2. The primary objective is: To determine the rate of complete hematologic respon...

What is the current status of trial NCT01350947?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 11 participants. The study started on 2011-04. Estimated completion is 2014-09.

What conditions does trial NCT01350947 study?

This clinical trial studies the following conditions: Chronic Myelomonocytic Leukemia. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT01350947?

The interventions under investigation include: 5-Azacitidine (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT01350947?

This trial is sponsored by University of Utah, which has 686 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT01350947 being conducted?

This trial has 3 study locations across New York, Oregon, Utah. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial