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Completed Phase 2 Interventional Results available

A Phase II Evaluation of Dasatinib (Sprycel®, NSC #732517) in the Treatment of Persistent or Recurrent Epithelial Ovarian, Fallopian Tube, or Primary Peritoneal Carcinoma

ClinicalTrials.gov ID: NCT00671788

Public ClinicalTrials.gov record NCT00671788. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Sep 23, 2026, 10:06 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

Dasatinib may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth. This phase II trial is studying how well dasatinib works in treating patients with persistent or recurrent ovarian epithelial cancer, fallopian tube cancer, or primary peritoneal cancer.

Study identification

NCT ID
NCT00671788
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Gynecologic Oncology Group
Network
Enrollment
35 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years and older
Sex
Female
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
May 31, 2008
Primary completion
Nov 30, 2010
Completion
Not listed
Last update posted
Apr 14, 2016

Started 2008

United States locations

U.S. sites
20
U.S. states
15
U.S. cities
20
Facility City State ZIP Site status
Saint Francis Hospital and Medical Center Hartford Connecticut 06105
The Hospital of Central Connecticut New Britain Connecticut 06050
Sarasota Memorial Hospital Sarasota Florida 34239
University of Chicago Comprehensive Cancer Center Chicago Illinois 60637
Indiana University/Melvin and Bren Simon Cancer Center Indianapolis Indiana 46202
University of Iowa Hospitals and Clinics Iowa City Iowa 52242
Ozark Health Ventures LLC-Cancer Research for The Ozarks Springfield Springfield Missouri 65804
Washington University School of Medicine St Louis Missouri 63110
Stony Brook University Medical Center Stony Brook New York 11794
Carolinas Medical Center Charlotte North Carolina 28203
University of Oklahoma Health Sciences Center Oklahoma City Oklahoma 73104
Tulsa Cancer Institute Tulsa Oklahoma 74146
Abington Memorial Hospital Abington Pennsylvania 19001
Fox Chase Cancer Center Philadelphia Pennsylvania 19111
Women and Infants Hospital Providence Rhode Island 02905
AnMed Health Cancer Center Anderson South Carolina 29621
Upstate Carolina CCOP Spartanburg South Carolina 29303
Huntsman Cancer Institute/University of Utah Salt Lake City Utah 84112
University of Virginia Charlottesville Virginia 22908
University of Wisconsin Hospital and Clinics Madison Wisconsin 53792

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00671788, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Apr 14, 2016 · Synced Sep 23, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00671788 live on ClinicalTrials.gov.

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