Comparison of Fulvestrant (FASLODEX™) 250 mg and 500 mg in Postmenopausal Women With Oestrogen Receptor Positive Advanced Breast Cancer Progressing or Relapsing After Previous Endocrine Therapy. (NCT00099437)
A Randomised, Double-Blind, Parallel-group, Multicentre, Phase III Study Comparing the Efficacy and Tolerability of Fulvestrant (FASLODEX™) 500 mg With Fulvestrant (FASLODEX™) 250 mg in Postmenopausal Women With Oestrogen Receptor Positive Advanced Breast Cancer Progressing or Relapsing After Previous Endocrine Therapy
🩺 Plain-English Summary (8th-Grade Level)
The purpose of this study is to evaluate the efficacy of a new dose of 500 mg Fulvestrant with the standard dose of 250 mg in postmenopausal women with oestrogen receptor positive advanced breast cancer who have failed on a previous endocrine treatment.
Who can join: Review the eligibility criteria below.
Location: Research Site — Casa Grande, Arizona
Age range: 45 Years to 130 Years
🧪 Interventions in This Study
📋 "Do I Qualify?" — 1-Minute Self Screener
Instant ChecklistFull eligibility criteria are available on the official NIH protocol. View the criteria ↗
📍 All Participating Trial Locations (106 Sites)
Showing the first 25 of 106 sites.
- Research Site — Casa Grande, Arizona
- Research Site — Fountain Valley, California
- Research Site — New Britain, Connecticut
- Research Site — Crystal River, Florida
- Research Site — Fort Lauderdale, Florida
- Research Site — Urbana, Illinois
- Research Site — Rosedale, Maryland
- Research Site — Detroit, Michigan
- Research Site — Kansas City, Missouri
- Research Site — St Louis, Missouri
- Research Site — Voorhees Township, New Jersey
- Research Site — Greenville, North Carolina
- Research Site — Pasadena, Texas
- Research Site — West Bend, Wisconsin
- Research Site — Brasschaat,
- Research Site — Brussels,
- Research Site — Brussels,
- Research Site — Edegem,
- Research Site — Ghent,
- Research Site — Hasselt,
- Research Site — Liège,
- Research Site — Turnhout,
- Research Site — Barretos,
- Research Site — Londrina,
- Research Site — Porto Alegre,
💰 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 § 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.
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💡 How to Participate
- Check the checklist above to see if you may qualify.
- Review the official NIH record below to find the coordinating site.
- Ask about the visit schedule, what is covered at no cost, and any travel support.
- Confirm with your own doctor before making a decision.