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NCT00939809 · ClinicalTrials.gov registry record · Phase 2

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

A Phase 2 study of Recurrent Ovarian Carcinoma and Primary Peritoneal Carcinoma, sponsored by Gynecologic Oncology Group.

Completed
Registry status
Phase 2
Development phase
31
Enrollment target
16
Study locations

NCT00939809: Completed Phase 2 study of Recurrent Ovarian Carcinoma and Primary Peritoneal Carcinoma, sponsored by Gynecologic Oncology Group.

NCT00939809 is a Phase 2 study of Recurrent Ovarian Carcinoma and Primary Peritoneal Carcinoma that has completed, run by Gynecologic Oncology Group. The registered enrollment target is 31 participants, below the 123-participant average among 39 other Recurrent Ovarian Carcinoma trials with a reported enrollment target (75% lower). The trial reports 16 study locations across 11 states. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00939809, a Phase 2 study of Recurrent Ovarian Carcinoma and Primary Peritoneal Carcinoma, has completed, sponsored by Gynecologic Oncology Group.

COMPLETED
Registry status
Phase 2
Development phase
31 participants
Enrollment target
16
Study locations

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.

Primary Outcome

Progression is defined using Response Evaluation Criteria In Solid Tumors Criteria (RECIST v1.0), as a 20% increase in the sum of the longest diameter (LD) of target lesions taking as reference the smallest sum LD recorded since study entry, or unequivocal progression of existing non-target lesions, or the appearance of one or more new lesions. CT scan or MRI is used to follow lesion for measurable disease every other cycle for the first 6 months; every three months thereafter; and at any time

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
Gynecologic Oncology Group

154 total trials

What the finished NCT00939809 record still lists

NCT00939809 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 31 participants, a relatively small participant target, below the 123-participant average among 39 other Recurrent Ovarian Carcinoma trials with a reported enrollment target (75% lower).

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.

NCT00939809 lists 16 locations in 11 states (Ohio, Pennsylvania, Georgia).

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.

What interventions are being tested in trial NCT00939809?

The interventions under investigation include: Laboratory Biomarker Analysis (OTHER), Urokinase-Derived Peptide A6 (BIOLOGICAL).

Who is sponsoring clinical trial NCT00939809?

This trial is sponsored by Gynecologic Oncology Group, which has 154 total clinical trials registered on ClinicalTrials.gov.

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.

Similar trials for Recurrent Ovarian Carcinoma

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT00939809's enrollment target sits among peer trials

31 28th of 39 higher than 11 of 39 other Recurrent Ovarian Carcinoma trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Recurrent Ovarian Carcinoma trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT00939809, the US trial registry maintained by the National Library of Medicine. NCT00939809 (small enrollment · multi site footprint · completed) retrieved and formatted by PlainTrial, see methodology.