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COMPLETED Phase 2

Study Of The Efficacy And Safety Of SU-014813 In Patients With Metastatic Breast Cancer

NCT00322517 · View on ClinicalTrials.gov ↗

Study Summary

To determine the antitumor efficacy and the safety of SU-014813 at a dose of 100 mg orally once daily in patients with Metastatic Breast Cancer

Conditions Studied

Interventions

  • DRUG SU014813

Study Locations (20)

Other

  • Pfizer Investigational Site — Hamburg
  • Pfizer Investigational Site — Magdeburg
  • Pfizer Investigational Site — Marburg
  • Pfizer Investigational Site — Chieti Scalo
  • Pfizer Investigational Site — Milan
  • Pfizer Investigational Site — Mirano (VE)
  • Pfizer Investigational Site — Udine
  • Pfizer Investigational Site — Amsterdam
  • Pfizer Investigational Site — Rotterdam
  • Pfizer Investigational Site — Edinburgh

California

  • Pfizer Investigational Site — Los Angeles
  • Pfizer Investigational Site — Pasadena
  • Pfizer Investigational Site — Santa Monica
  • Pfizer Investigational Site — Valancia

Mississippi

  • Pfizer Investigational Site — Corinth
  • Pfizer Investigational Site — Southaven

Tennessee

  • Pfizer Investigational Site — Memphis
  • Pfizer Investigational Site — Memphis

M20 4bx

  • Pfizer Investigational Site — Manchester

Surrey

  • Pfizer Investigational Site — Sutton

Trial Details

FieldValue
Enrollment Target 90 participants
Start Date 2006-04
Est. Completion 2009-07
Phase Phase 2

Sponsor

Pfizer

769 total trials

Interested in This Trial?

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT00322517

The ClinicalTrials.gov registry entry for NCT00322517 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 90 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Pfizer, which has 769 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 Breast Neoplasms appearing as the primary indexed condition, and to 1 intervention — of which SU014813 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: NCT00322517 reports 20 study locations spanning 6 distinct geographic areas — top geographies include Other, California, Mississippi. 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 NCT00322517 about?

NCT00322517 is a clinical study titled "Study Of The Efficacy And Safety Of SU-014813 In Patients With Metastatic Breast Cancer". To determine the antitumor efficacy and the safety of SU-014813 at a dose of 100 mg orally once daily in patients with Metastatic Breast Cancer

What is the current status of trial NCT00322517?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 90 participants. The study started on 2006-04. Estimated completion is 2009-07.

What conditions does trial NCT00322517 study?

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

What interventions are being tested in trial NCT00322517?

The interventions under investigation include: SU014813 (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT00322517?

This trial is sponsored by Pfizer, which has 769 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT00322517 being conducted?

This trial has 20 study locations across California, Mississippi, Tennessee, M20 4bx, Surrey. 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