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CompletedNCT00083278Updated Apr 27, 2012

Study of MDX-010 in Stage IV Breast Cancer

A Phase 2 interventional study of MDX-010 in Breast Cancer and Adenocarcinoma, sponsored by Bristol-Myers Squibb. Completed at 14 sites in United States. Open to female participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2012-04-27.

Sponsored by Bristol-Myers Squibb · Phase 2, Interventional, and Treatment

Phase
Phase 2
Study type
Interventional
Enrollment
33
Allocation
Non-randomized
Ages
18 Years and older
Sex
Female
01

Study summary

This Phase II study is designed to treat patients who have been diagnosed with Stage IV Breast Cancer, which has progressed despite treatment with primary therapies, including hormonal therapy, chemotherapy, and antibody therapy. Thirty-three patients will be treated with the monoclonal antibody MDX-010. The initial antitumor activity profile of MDX-010 will be determined, as well as identification of the induction of any antitumor immunity following the MDX-010 treatment.

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Conditions studied

  • Breast Cancer
  • Adenocarcinoma

Keywords

  • Breast Cancer
  • Stage IV adenocarcinoma of the breast
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In context

Breast Neoplasms

12,547 studies on the registry are indexed under Breast Neoplasms; 2,892 are open to participants now.

This study's enrollment of 33 is below the median of 72 across 9,305 interventional studies indexed under Breast Neoplasms.

Browse Breast Neoplasms studies →

Lead sponsor

Bristol-Myers Squibb is the lead sponsor of 1,538 studies on the registry; 116 are open to participants now.

Of its 429 completed or terminated interventional studies of FDA-regulated products, 223 (52%) have results posted.

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

04

Who can participate

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

Inclusion criteria

  • Provide written informed consent
  • diagnosed with Stage IV adenocarcinoma that has progressed despite previous therapy
  • at least 18 years of age
  • measurable disease defined by RECIST
  • must discontinue any alternative therapy used to treat breast cancer at least 4 weeks prior to enrollment and agree to not use such therapies during the duration of the study (patients may continue to receive tamoxifen, bisphosphate therapy and trastuzumab)
  • prior radiation must be completed at least 4 weeks prior to enrollment
  • ECOG performance status of 0-2
  • Negative pregnancy test
  • Screening lab values must be met

Exclusion criteria

Exclusion Criteria:

  • must be disease free from other cancers for at least 5 years
  • symptomatic or untreated brain metastases
  • active or history of autoimmune disease
  • active HIV, HTLV, HBV or HCV infection
  • concurrent medical condition requiring the use of systemic corticosteroids, must be discontinued at least 4 weeks prior to enrollment
  • prior therapy with anti-CTLA-4 antibody
  • significant organ compromise, uncontrolled heart, liver, lung, or renal disease or other serious illness
  • pregnancy or nursing
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Study design

Phase
Phase 2
Primary purpose
Treatment
Allocation
Non-randomized
Masking
None (open label)
Enrollment
33 participants (actual)

Interventions

  • DrugMDX-010
06

Study locations

14 sites
  • Sharp Clinical Oncology Research
    San Diego, California 92123, United States
  • Wishard Health Services
    Indianapolis, Indiana 46202-2859, United States
  • Section of Hematology/Oncology, Indiana Cancer Pavilion
    Indianapolis, Indiana 46202-5289, United States
  • Indiana University, Clarian Health Partners
    Indianapolis, Indiana 46202, United States
  • Medical Arts Building
    Jeffersonville, Indiana 47130, United States
  • Kansas City Oncology and Hematology Group
    Kansas City, Kansas 66112, United States
  • Kansas City Oncology and Hematology Group
    Overland Park, Kansas 66210, United States
  • LaGrange
    LaGrange, Kentucky 40031, United States
  • Norton Healthcare Inc, Loiusville Oncology Clinical Research Program
    Louisville, Kentucky 40202, United States
  • Suburban Medical Plaza II
    Louisville, Kentucky 40207, United States
  • Audubon Oncology/Hematology
    Louisville, Kentucky 40217, United States
  • Kansas City Oncology and Hematology Group
    Kansas City, Missouri 64131, United States
  • Kansas City Oncology and Hematology Group
    Lee's Summit, Missouri 64064, United States
  • Arlington Cancer Center
    Arlington, Texas 76012, United States
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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Apr 27, 2012, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT00083278
Lead sponsor
Bristol-Myers Squibb
First posted
May 20, 2004
Start date
May 2003
Completion
Feb 2006
Last update
Apr 27, 2012

Study contacts

Bristol-Myers Squibb
study director · Bristol-Myers Squibb
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Apr 2012. You cannot join it, but the record below documents what was studied.

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