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NCT00546780 · ClinicalTrials.gov registry record · Phase 3

A Study of Tanespimycin (KOS-953) in Patients With Multiple Myeloma in First Relapse

A Phase 3 study of Multiple Myeloma, sponsored by Bristol-Myers Squibb.

Completed
Registry status
Phase 3
Development phase
31
Enrollment target
19
Study locations

NCT00546780 is a Phase 3 study of Multiple Myeloma that has completed, run by Bristol-Myers Squibb. The registered enrollment target is 31 participants, below the 547-participant average among 438 other Multiple Myeloma trials with a reported enrollment target (94% lower). The trial reports 19 study locations across 16 states.

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The verdict

NCT00546780, a Phase 3 study of Multiple Myeloma, has completed, sponsored by Bristol-Myers Squibb.

COMPLETED
Registry status
Phase 3
Development phase
31 participants
Enrollment target
19
Study locations

Study Summary

This is a phase 3, open label trial for patients with multiple myeloma in first relapse. Trial will compare tanespimycin (KOS-953), in combination with a fixed dose of bortezomib versus bortezomib alone.

Conditions Studied

Interventions

  • DRUG Bortezomib
  • DRUG Tanespimycin

Study Locations (19)

California

  • Comprehensive Blood And Cancer Center - Bakersfield
  • Moores Ucsd Cancer Center - La Jolla
  • University Of California Medical Center - San Francisco

Tennessee

  • Tennessee Cancer Specialists - Knoxville
  • Sarah Cannon Research Institute - Nashville

Colorado

  • Rocky Mountain Cancer Centers - Denver

Iowa

  • University Of Iowa Hospitals And Clinics - Iowa City

Kansas

  • University Of Kansas Medical Center - Westwood

Massachusetts

  • Dana-Farber Cancer Institute - Boston

Michigan

  • Henry Ford Health System Irb - Detroit

Missouri

  • Capitol Comprehensive Cancer Care Center - Jefferson City

Trial Details

FieldValue
Enrollment Target 31 participants
Start Date 2008-02
Est. Completion 2010-03
Phase Phase 3

Sponsor

Bristol-Myers Squibb

1,025 total trials

What the Registry Record Tells You About NCT00546780

The ClinicalTrials.gov registry entry for NCT00546780 describes a study currently listed as completed, categorized as Phase 3. The registered enrollment target is 31 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 547-participant average among 438 other Multiple Myeloma trials with a reported enrollment target (94% lower). The listed sponsor is Bristol-Myers Squibb, which has 1,025 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Multiple Myeloma appearing as the primary indexed condition, and to 2 interventions - of which Bortezomib is the first listed.

NCT00546780 reports 19 study locations spanning 16 distinct geographic areas - top geographies include California, Tennessee, Colorado.

Frequently Asked Questions

What is clinical trial NCT00546780 about?

NCT00546780 is a clinical study titled "A Study of Tanespimycin (KOS-953) in Patients With Multiple Myeloma in First Relapse". This is a phase 3, open label trial for patients with multiple myeloma in first relapse. Trial will compare tanespimycin (KOS-953), in combination with a fixed dose of bortezomib versus bortezomib alone.

What is the current status of trial NCT00546780?

This trial is currently completed. It is a Phase 3 study. The enrollment target is 31 participants. The study started on 2008-02. Estimated completion is 2010-03.

What conditions does trial NCT00546780 study?

This clinical trial studies the following conditions: Multiple Myeloma.

What interventions are being tested in trial NCT00546780?

The interventions under investigation include: Bortezomib (DRUG), Tanespimycin (DRUG).

Who is sponsoring clinical trial NCT00546780?

This trial is sponsored by Bristol-Myers Squibb, which has 1,025 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT00546780 being conducted?

This trial has 19 study locations across California, Colorado, Iowa, Kansas, Massachusetts. 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

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.