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COMPLETED Phase 2

Phase 2 Study MPC-6827 for Recurrent Glioblastoma Multiforme

NCT00892931 · View on ClinicalTrials.gov ↗

Study Summary

The purpose of this study is to determine the safety and effectiveness of Azixa in patients with recurrent glioblastoma multiforme

Conditions Studied

Interventions

  • DRUG Azixa

Study Locations (10)

Massachusetts

  • Tufts Medical Center — Boston
  • Lahey Clinic — Burlington
  • University of Massachusettes — Worcester

California

  • Cedars-Sinai Medical Center — Los Angeles
  • Stanford University — Stanford

Arizona

  • Barrow Neurological Institute — Phoenix

Illinois

  • Northwestern University — Chicago

New Hampshire

  • Darthmouth -Hitchcock Medical Center — Lebanon

New York

  • Columbia University — New York

Washington

  • SCCA/University of Washington — Seattle

Trial Details

FieldValue
Enrollment Target 56 participants
Start Date 2009-04
Est. Completion 2011-09
Phase Phase 2

Sponsor

Myrexis

2 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT00892931

The ClinicalTrials.gov registry entry for NCT00892931 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 56 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Myrexis, which has 2 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 Glioblastoma Multiforme appearing as the primary indexed condition, and to 1 intervention — of which Azixa 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: NCT00892931 reports 10 study locations spanning 7 distinct geographic areas — top geographies include Massachusetts, California, Arizona. 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 NCT00892931 about?

NCT00892931 is a clinical study titled "Phase 2 Study MPC-6827 for Recurrent Glioblastoma Multiforme". The purpose of this study is to determine the safety and effectiveness of Azixa in patients with recurrent glioblastoma multiforme

What is the current status of trial NCT00892931?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 56 participants. The study started on 2009-04. Estimated completion is 2011-09.

What conditions does trial NCT00892931 study?

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

What interventions are being tested in trial NCT00892931?

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

Who is sponsoring clinical trial NCT00892931?

This trial is sponsored by Myrexis, which has 2 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT00892931 being conducted?

This trial has 10 study locations across Arizona, California, Illinois, Massachusetts, New Hampshire. 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