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WithdrawnNCT00380835Updated Sep 23, 2008

Study of Amrubicin With or Without Herceptin in Patients With Metastatic Breast Cancer

A Phase 2 interventional study of Amrubicin in Metastatic Breast Cancer, sponsored by Celgene Corporation. Withdrawn at 28 sites in United States. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2008-09-23.

Sponsored by Celgene Corporation · Phase 2, Interventional, and Treatment

Why this study was withdrawn
Study Never Initiated
Phase
Phase 2
Study type
Interventional
Enrollment
66
Allocation
Non-randomized
Ages
18 Years and older
Sex
All
01

Study summary

The purpose of the study is to evaluate the incidence of cardiac toxicity of amrubicin when administered to patients with metastatic breast cancer.

02

Conditions studied

  • Metastatic Breast Cancer

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Keywords

  • metastatic breast cancer
  • amrubicin
03

In context

Breast Neoplasms

12,544 studies on the registry are indexed under Breast Neoplasms; 2,892 are open to participants now.

This study's planned enrollment of 66 is close to the median of 72 across 9,303 interventional studies indexed under Breast Neoplasms.

Browse Breast Neoplasms studies →

Lead sponsor

Celgene Corporation is the lead sponsor of 50 studies on the registry; none are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Histological or cytological diagnosis of breast cancer.
  • Metastatic or recurrent disease, either HER2+ (FISH+ or 3+ IHC) or HER2-.
  • Maximal dose of prior adjuvant anthracycline: 300 mg/meters squared doxorubicin or equivalent. Relapse greater than one year after trastuzumab adjuvantly; two years following adjuvant anthracycline therapy (without trastuzumab).
  • One prior chemotherapy for metastatic breast cancer allowed (may include trastuzumab for HER2+ patients), but no prior Doxil, adriamycin or epirubicin for metastatic breast cancer.
  • At least 18 years of age.
  • ECOG Performance Status of 0, 1, or 2.
  • Adequate organ function including the following:

    • Adequate bone marrow reserve.
    • Cardiac: Left ventricular ejection fraction (LVEF) greater than or equal to 55% by MUGA.
  • Negative serum pregnancy test at the time of enrollment for women of child-bearing potential.
  • Ability to understand the requirements of the study, provide written informed consent and authorization of use and disclosure of protected health information, and agree to abide by the study restrictions and to return for the required assessments.

Exclusion criteria

Exclusion Criteria:

  • Pregnant or nursing women.
  • Concurrent anticancer therapy.
  • Participation in any investigational drug study within 28 days prior to study entry.
  • Concurrent severe or uncontrolled medical disease (i.e., active systemic infection, diabetes, uncontrolled hypertension, coronary artery disease, congestive heart failure, severe arrhythmia) that, in the opinion of the Investigator, would compromise the safety of the patient or compromise the ability of the patient to complete the study.
  • Symptomatic central nervous system metastases. Patients with asymptomatic brain metastases are allowed. The patient must be stable after radiotherapy for greater than or equal to 2 weeks and off corticosteroids for greater than or equal to 1 week.
  • History of interstitial lung disease or pulmonary fibrosis.
05

Study design

Phase
Phase 2
Primary purpose
Treatment
Allocation
Non-randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
66 participants (estimated)

Interventions

  • DrugAmrubicin
06

What researchers measure

Primary outcomes

  1. Incidence of cardiac toxicity

Secondary outcomes

  1. Objective tumor response rate according to RECIST criteria measured every 2 cycles (every 6 weeks)

  2. Duration of overall response

  3. Time to tumor progression

  4. Progression free survival

  5. Toxicity profile

07

Study locations

28 sites
  • New Milford, Connecticut 06776, United States
  • Sharon, Connecticut 06069, United States
  • Torrington, Connecticut 06790, United States
  • Burnsville, Minnesota 55337, United States
  • Edina, Minnesota 55435-2150, United States
  • Maplewood, Minnesota 55109, United States
  • Minneapolis, Minnesota 55404, United States
  • St. Paul, Minnesota 55102-2389, United States
  • Woodbury, Minnesota 55125, United States
  • Columbia, Missouri 65201, United States
  • Albany, New York 12208, United States
  • Amsterdam, New York 12010, United States
  • Hudson, New York 12534, United States
  • Latham, New York 12110-0610, United States
  • Rexford, New York 12148, United States
  • Schenectady, New York 12308, United States
  • Troy, New York 12180, United States
  • Asheville, North Carolina 28803, United States
  • Dallas, Texas 75230-2510, United States
  • Dallas, Texas 75231-4400, United States
  • Dallas, Texas 75246, United States
  • El Paso, Texas 79902, United States
  • El Paso, Texas 79915, United States
  • Houston, Texas 77024, United States
  • Midland, Texas 79701-5946, United States
  • Odessa, Texas 79761, United States
  • Plano, Texas 75075-7787, United States
  • Tyler, Texas 75702, United States
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Sep 23, 2008, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT00380835
Lead sponsor
Celgene Corporation
First posted
Sep 27, 2006
Completion
Dec 2007
Last update
Sep 23, 2008

Study contacts

Richard S Ungerleider, MD
study director · Theradex
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is withdrawn, as verified in Sep 2008. You cannot join it, but the record below documents what was studied.

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