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NCT00326885 · ClinicalTrials.gov registry record · Phase 2

Study of the Trifunctional Antibody Catumaxomab to Treat Recurrent Symptomatic Malignant Ascites

A Phase 2 study of Malignant Ascites, sponsored by Neovii Biotech.

Completed
Registry status
Phase 2
Development phase
32
Enrollment target
18
Study locations

NCT00326885 is a Phase 2 study of Malignant Ascites that has completed, run by Neovii Biotech. The registered enrollment target is 32 participants. The trial reports 18 study locations across 15 states.

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The verdict

NCT00326885, a Phase 2 study of Malignant Ascites, has completed, sponsored by Neovii Biotech.

COMPLETED
Registry status
Phase 2
Development phase
32 participants
Enrollment target
18
Study locations

Study Summary

The purpose of this study is to determine whether the investigational drug catumaxomab is a safe and effective treatment for recurrent symptomatic malignant ascites.

Conditions Studied

Interventions

  • DRUG catumaxomab

Study Locations (18)

California

  • University of San Diego - La Jolla
  • Stanford University Hospital and Clinics - Stanford

Florida

  • University of Miami - Miami
  • Florida Hospital Cancer Center - Orlando

Massachusetts

  • Dana Farber Cancer Institute - Boston
  • Massachusetts General Hospital - Boston

Arizona

  • University of Arizona Cancer Center - Tucson

Indiana

  • Northern Indiana Cancer Research Consortium - South Bend

Kentucky

  • University of Louisville Cancer Center - Louisville

Maryland

  • Johns Hopkins Medical Institute - Baltimore

Michigan

  • Wayne State University - Detroit

Trial Details

FieldValue
Enrollment Target 32 participants
Start Date 2006-06
Est. Completion 2010-08
Phase Phase 2

Sponsor

Neovii Biotech

5 total trials

What the Registry Record Tells You About NCT00326885

The ClinicalTrials.gov registry entry for NCT00326885 describes a study currently listed as completed, categorized as Phase 2. The registered enrollment target is 32 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Neovii Biotech, which has 5 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Malignant Ascites appearing as the primary indexed condition, and to 1 intervention - of which catumaxomab is the first listed.

NCT00326885 reports 18 study locations spanning 15 distinct geographic areas - top geographies include California, Florida, Massachusetts.

Frequently Asked Questions

What is clinical trial NCT00326885 about?

NCT00326885 is a clinical study titled "Study of the Trifunctional Antibody Catumaxomab to Treat Recurrent Symptomatic Malignant Ascites". The purpose of this study is to determine whether the investigational drug catumaxomab is a safe and effective treatment for recurrent symptomatic malignant ascites.

What is the current status of trial NCT00326885?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 32 participants. The study started on 2006-06. Estimated completion is 2010-08.

What conditions does trial NCT00326885 study?

This clinical trial studies the following conditions: Malignant Ascites.

What interventions are being tested in trial NCT00326885?

The interventions under investigation include: catumaxomab (DRUG).

Who is sponsoring clinical trial NCT00326885?

This trial is sponsored by Neovii Biotech, which has 5 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT00326885 being conducted?

This trial has 18 study locations across Arizona, California, Florida, Indiana, Kentucky. 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.