๐Ÿ›๏ธ Verified NIH Record โ€ข Updated 2026-05-07

Male Breast Cancer: Understanding the Biology for Improved Patient Care (NCT01101425)

Clinical and Biological Characterization of Male Breast Cancer: an International EORTC, BIG, TBCRC and NABCG Intergroup Study.

๐Ÿ”ต Active, Not Recruiting Interventional Protocol ๐Ÿ“Š Observational Clinical Research Sponsor: European Organisation for Research and Treatment of Cancer - EORTC

๐Ÿฉบ Plain-English Summary (8th-Grade Level)

Rationale: Gathering medical information and tumor samples from patients with male breast cancer may help doctors learn more about the disease. Purpose retrospective part: to perform a large international retrospective analysis of clinical and biological data of male BC patients treated in the participating centers from 1990 to 2010. Purpose prospective part: to create a registry of men with breast cancer for a period of 30 months (starting early 2014).

Who can join: Review the eligibility criteria below.

Location: University Of Alabama Comprehensive Cancer Center โ€” Birmingham, Alabama

Age range: 18 Years

๐Ÿ“‹ "Do I Qualify?" โ€” 1-Minute Self Screener

Instant Checklist

Full eligibility criteria are available on the official NIH protocol. View the criteria โ†—

๐Ÿ“ All Participating Trial Locations (93 Sites)

Showing the first 25 of 93 sites.

  • University Of Alabama Comprehensive Cancer Center โ€” Birmingham, Alabama
  • University Of Alabama Comprehensive Cancer Cente โ€” Birmingham, Alabama
  • UCSF University of California San Francisco Medical Center-Mount Zion โ€” San Francisco, California
  • Georgetown Lombardi Comprehensive Cancer Center โ€” Washington D.C., District of Columbia
  • University of Chicago Medicine โ€” Chicago, Illinois
  • Indiana University Medical Center โ€” Indianapolis, Indiana
  • Johns Hopkins University CRB1 โ€” Baltimore, Maryland
  • Johns Hopkins University โ€” Baltimore, Maryland
  • Dana-Farber Cancer Institute โ€” Boston, Massachusetts
  • University of Michigan โ€” Ann Arbor, Michigan
  • Mayo Clinic โ€” Rochester, Minnesota
  • Memorial Sloan-Kettering Cancer Center - Memorial hospital โ€” New York, New York
  • Duke University Medical Center โ€” Durham, North Carolina
  • Baylor college of Medicine โ€” Houston, Texas
  • MD Anderson Cancer Center โ€” Houston, Texas
  • Baylor College - Ucop โ€” Houston, Texas
  • Fred Hutchison Seattle Cancer Care Alliance โ€” Seattle, Washington
  • ZNA Middelheim โ€” Antwerp,
  • Cliniques Universitaires Saint-Luc โ€” Brussels,
  • CHU St Pierre โ€” Brussels,
  • Cliniques Universitaires St. Luc โ€” Brussels,
  • Hopital Universitaire Brugmann โ€” Brussels,
  • Institut Jules Bordet โ€” Brussels,
  • Universitair Ziekenhuis Antwerpen โ€” Edegem,
  • Hopital De Jolimont โ€” Haine-Saint-Paul,

๐Ÿ’ฐ Cost, Insurance & Patient Rights

  • 100% Free Items: The investigational treatment and protocol-required procedures are supplied at zero cost by the sponsor.
  • Routine Patient Care: Under federal law (ACA ยง 2709) and many state statutes, routine care costs are covered during participation.
  • Voluntary Participation: You may withdraw at any time without affecting your standard medical care.

Explore by condition: All Breast Cancer clinical trials

๐Ÿ’ก How to Participate

  1. Check the checklist above to see if you may qualify.
  2. Review the official NIH record below to find the coordinating site.
  3. Ask about the visit schedule, what is covered at no cost, and any travel support.
  4. Confirm with your own doctor before making a decision.
๐Ÿ›๏ธ View Official NIH Record โ†—