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NCT00993616 · ClinicalTrials.gov registry record · Phase 2

Belinostat and Carboplatin in Treating Patients With Recurrent or Persistent Ovarian Epithelial Cancer, Fallopian Tube Cancer, or Primary Peritoneal Cancer That Did Not Respond to Carboplatin or Cisplatin

A Phase 2 study of Fallopian Tube Cancer and Primary Peritoneal Cavity Cancer, sponsored by National Cancer Institute (NCI).

Completed
Registry status
Phase 2
Development phase
29
Enrollment target
20
Study locations

NCT00993616 is a Phase 2 study of Fallopian Tube Cancer and Primary Peritoneal Cavity Cancer that has completed, run by National Cancer Institute (NCI). The registered enrollment target is 29 participants, below the 255-participant average among 85 other Fallopian Tube Cancer trials with a reported enrollment target (89% lower). The trial reports 20 study locations across 7 states.

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The verdict

NCT00993616, a Phase 2 study of Fallopian Tube Cancer and Primary Peritoneal Cavity Cancer, has completed, sponsored by National Cancer Institute (NCI).

COMPLETED
Registry status
Phase 2
Development phase
29 participants
Enrollment target
20
Study locations

Study Summary

This phase II trial is studying how well giving belinostat together with carboplatin works in treating patients with recurrent or persistent ovarian epithelial cancer, fallopian tube cancer, or primary peritoneal cancer that did not respond to carboplatin or cisplatin. Belinostat may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth and by blocking blood flow to the tumor. Drugs used in chemotherapy, such as carboplatin, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. Giving belinostat together with carboplatin may kill more tumor cells.

Interventions

  • DRUG carboplatin
  • DRUG belinostat

Study Locations (20)

Iowa

  • Medical Oncology and Hematology Associates-West Des Moines - Clive
  • Mercy Cancer Center-West Lakes - Clive
  • Iowa Methodist Medical Center - Des Moines
  • Iowa Oncology Research Association CCOP - Des Moines
  • Medical Oncology and Hematology Associates-Des Moines - Des Moines
  • Medical Oncology and Hematology Associates-Laurel - Des Moines
  • Mercy Medical Center - Des Moines - Des Moines
  • Iowa Lutheran Hospital - Des Moines
  • University of Iowa Hospitals and Clinics - Iowa City
  • Mercy Medical Center-West Lakes - West Des Moines

Kansas

  • Menorah Medical Center - Overland Park
  • Saint Luke's South Hospital - Overland Park
  • Shawnee Mission Medical Center - Shawnee Mission

Connecticut

  • Saint Francis Hospital and Medical Center - Hartford
  • The Hospital of Central Connecticut - New Britain

Delaware

  • Beebe Medical Center - Lewes
  • Christiana Care Health System-Christiana Hospital - Newark

Illinois

  • Rush University Medical Center - Chicago

Indiana

  • Indiana University Medical Center - Indianapolis

Maryland

  • Greater Baltimore Medical Center - Baltimore

Trial Details

FieldValue
Enrollment Target 29 participants
Start Date 2009-12
Est. Completion 2012-07-29
Phase Phase 2

Sponsor

National Cancer Institute (NCI)

3,257 total trials

What the Registry Record Tells You About NCT00993616

The ClinicalTrials.gov registry entry for NCT00993616 describes a study currently listed as completed, categorized as Phase 2. The registered enrollment target is 29 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 255-participant average among 85 other Fallopian Tube Cancer trials with a reported enrollment target (89% lower). The listed sponsor is National Cancer Institute (NCI), which has 3,257 total studies on file at ClinicalTrials.gov.

The record links to 10 conditions, with Fallopian Tube Cancer appearing as the primary indexed condition, and to 2 interventions - of which carboplatin is the first listed.

NCT00993616 reports 20 study locations spanning 7 distinct geographic areas - top geographies include Iowa, Kansas, Connecticut.

Frequently Asked Questions

What is clinical trial NCT00993616 about?

NCT00993616 is a clinical study titled "Belinostat and Carboplatin in Treating Patients With Recurrent or Persistent Ovarian Epithelial Cancer, Fallopian Tube Cancer, or Primary Peritoneal Cancer That Did Not Respond to Carboplatin or Cisplatin". This phase II trial is studying how well giving belinostat together with carboplatin works in treating patients with recurrent or persistent ovarian epithelial cancer, fallopian tube cancer, or primary peritoneal cancer that did not respond to carboplatin or cisplatin. Belinostat may stop the growth...

What is the current status of trial NCT00993616?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 29 participants. The study started on 2009-12. Estimated completion is 2012-07-29.

What conditions does trial NCT00993616 study?

This clinical trial studies the following conditions: Fallopian Tube Cancer, Primary Peritoneal Cavity Cancer, Ovarian Endometrioid Adenocarcinoma, Recurrent Ovarian Epithelial Cancer, Ovarian Mucinous Cystadenocarcinoma.

What interventions are being tested in trial NCT00993616?

The interventions under investigation include: carboplatin (DRUG), belinostat (DRUG).

Who is sponsoring clinical trial NCT00993616?

This trial is sponsored by National Cancer Institute (NCI), which has 3,257 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT00993616 being conducted?

This trial has 20 study locations across Connecticut, Delaware, Illinois, Indiana, Iowa. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.