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NCT00035113 · ClinicalTrials.gov registry record · Phase 2

EPO906 Therapy in Patients With Prostate Cancer

A Phase 2 study of Prostatic Neoplasms, sponsored by Novartis Pharmaceuticals.

Completed
Registry status
Phase 2
Development phase
48
Enrollment target
5
Study locations

NCT00035113 is a Phase 2 study of Prostatic Neoplasms that has completed, run by Novartis Pharmaceuticals. The registered enrollment target is 48 participants, below the 514-participant average among 65 other Prostatic Neoplasms trials with a reported enrollment target (91% lower). The trial reports 5 study locations across 4 states.

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The verdict

NCT00035113, a Phase 2 study of Prostatic Neoplasms, has completed, sponsored by Novartis Pharmaceuticals.

COMPLETED
Registry status
Phase 2
Development phase
48 participants
Enrollment target
5
Study locations

Study Summary

This study will examine whether the new investigational drug EPO906, given by intravenous infusion (IV directly into the vein), is effective in shrinking tumors and preventing the growth of cells that cause prostate cancer.

Conditions Studied

Interventions

  • DRUG epothilone b

Study Locations (5)

California

  • Pacific Shores Medical Group - Long Beach
  • California Pacific Medical Center - San Francisco

Maryland

  • University of Maryland - Greenbaum Cancer Center - Baltimore

New Jersey

  • Cancer Institute of New Jersey (CINJ) - New Brunswick

Washington

  • Seattle Cancer Care Alliance - Seattle

Trial Details

FieldValue
Enrollment Target 48 participants
Start Date 2002-01
Est. Completion 2004-01
Phase Phase 2

Sponsor

Novartis Pharmaceuticals

1,375 total trials

What the Registry Record Tells You About NCT00035113

The ClinicalTrials.gov registry entry for NCT00035113 describes a study currently listed as completed, categorized as Phase 2. The registered enrollment target is 48 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 514-participant average among 65 other Prostatic Neoplasms trials with a reported enrollment target (91% lower). The listed sponsor is Novartis Pharmaceuticals, which has 1,375 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Prostatic Neoplasms appearing as the primary indexed condition, and to 1 intervention - of which epothilone b is the first listed.

NCT00035113 reports 5 study locations spanning 4 distinct geographic areas - top geographies include California, Maryland, New Jersey.

Frequently Asked Questions

What is clinical trial NCT00035113 about?

NCT00035113 is a clinical study titled "EPO906 Therapy in Patients With Prostate Cancer". This study will examine whether the new investigational drug EPO906, given by intravenous infusion (IV directly into the vein), is effective in shrinking tumors and preventing the growth of cells that cause prostate cancer.

What is the current status of trial NCT00035113?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 48 participants. The study started on 2002-01. Estimated completion is 2004-01.

What conditions does trial NCT00035113 study?

This clinical trial studies the following conditions: Prostatic Neoplasms.

What interventions are being tested in trial NCT00035113?

The interventions under investigation include: epothilone b (DRUG).

Who is sponsoring clinical trial NCT00035113?

This trial is sponsored by Novartis Pharmaceuticals, which has 1,375 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT00035113 being conducted?

This trial has 5 study locations across California, Maryland, New Jersey, Washington. 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.