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Higher dose of breast cancer drug shows promise in early trial

NCT ID NCT00585507

First seen May 27, 2026 · Last updated Jun 19, 2026 · Updated 5 times

Summary

This phase II trial is testing a higher dose (500 mg) of the drug fulvestrant (Faslodex) as a first hormonal treatment for postmenopausal women with hormone receptor positive metastatic breast cancer. The study aims to see if this higher dose improves clinical benefit compared to standard doses. Forty women are enrolled to receive injections on a monthly schedule.

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This is a summary of the original study . Summaries may miss details or leave out important information. Before applying or accepting participation, make sure you have read and understood the full study. Curemydisease.com takes no responsibility whatsoever for anything missed, misunderstood, or acted upon as a result of our summary — we know it does not capture everything.

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Contacts and locations

Locations

  • Beth Israel Deaconess Medical Center

    Boston, Massachusetts, 02115, United States

  • Dana-Farber Cancer Institute

    Boston, Massachusetts, 02115, United States

  • Lowell General Hospital

    Lowell, Massachusetts, 01854, United States

  • Massachusetts General Hosptial

    Boston, Massachusetts, 02114, United States

  • South Shore Hospital

    South Weymouth, Massachusetts, 02190, United States

What this could mean

Our plain-language read of the trial. This is informational only — not medical advice or a prediction.

Active substance

Fulvestrant (Faslodex)

What this could lead to

If successful, this higher dose of fulvestrant could improve control of metastatic breast cancer, offering a more effective first-line hormonal therapy option.

What could go wrong

This is a small phase II trial with only 40 participants, so results may not apply broadly. The higher dose could also increase side effects without improving outcomes.

Conditions

The condition(s) this trial relates to.

breast cancer breast neoplasm hormone receptor-positive breast cancer

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.