Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

COMPLETED Phase 2

A6 in Treating Patients With Persistent or Recurrent Ovarian Epithelial Cancer, Fallopian Tube Cancer, or Primary Peritoneal Cancer

NCT00939809 · View on ClinicalTrials.gov ↗

Study Summary

This phase II trial is studying the side effects and how well A6 works in treating patients with persistent or recurrent ovarian epithelial cancer, fallopian tube cancer, or primary peritoneal cancer. A6 may stop the growth of tumor cells by blocking blood flow to the tumor.

Interventions

  • OTHER Laboratory Biomarker Analysis
  • BIOLOGICAL Urokinase-Derived Peptide A6

Study Locations (16)

Ohio

  • Case Western Reserve University — Cleveland
  • MetroHealth Medical Center — Cleveland
  • Cleveland Clinic Cancer Center/Fairview Hospital — Cleveland
  • Riverside Methodist Hospital — Columbus
  • Hillcrest Hospital Cancer Center — Mayfield Heights

Pennsylvania

  • Abington Memorial Hospital — Abington
  • Magee-Womens Hospital of UPMC — Pittsburgh

Georgia

  • Georgia Regents University Medical Center — Augusta

Iowa

  • University of Iowa Hospitals and Clinics — Iowa City

Nebraska

  • Nebraska Methodist Hospital — Omaha

New York

  • Stony Brook University Medical Center — Stony Brook

Oklahoma

  • University of Oklahoma Health Sciences Center — Oklahoma City

Rhode Island

  • Women and Infants Hospital — Providence

Trial Details

FieldValue
Enrollment Target 31 participants
Start Date 2009-07
Phase Phase 2

Sponsor

Gynecologic Oncology Group

61 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT00939809

The ClinicalTrials.gov registry entry for NCT00939809 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 31 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Gynecologic Oncology Group, which has 61 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 10 conditions, with Recurrent Ovarian Carcinoma appearing as the primary indexed condition, and to 2 interventions — of which Laboratory Biomarker Analysis 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: NCT00939809 reports 16 study locations spanning 11 distinct geographic areas — top geographies include Ohio, Pennsylvania, Georgia. 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 NCT00939809 about?

NCT00939809 is a clinical study titled "A6 in Treating Patients With Persistent or Recurrent Ovarian Epithelial Cancer, Fallopian Tube Cancer, or Primary Peritoneal Cancer". This phase II trial is studying the side effects and how well A6 works in treating patients with persistent or recurrent ovarian epithelial cancer, fallopian tube cancer, or primary peritoneal cancer. A6 may stop the growth of tumor cells by blocking blood flow to the tumor.

What is the current status of trial NCT00939809?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 31 participants. The study started on 2009-07.

What conditions does trial NCT00939809 study?

This clinical trial studies the following conditions: Recurrent Ovarian Carcinoma, Primary Peritoneal Carcinoma, Ovarian Endometrioid Adenocarcinoma, Fallopian Tube Carcinoma, Ovarian Brenner Tumor. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT00939809?

The interventions under investigation include: Laboratory Biomarker Analysis (OTHER), Urokinase-Derived Peptide A6 (BIOLOGICAL). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT00939809?

This trial is sponsored by Gynecologic Oncology Group, which has 61 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT00939809 being conducted?

This trial has 16 study locations across Georgia, Iowa, Nebraska, New York, Ohio. 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