Could tailored tamoxifen doses keep more breast cancer patients on treatment?

NCT ID NCT07502820

First seen Jun 27, 2026 · Last updated Aug 13, 2026 · Updated 2 times

Summary

This phase 3 trial tests whether adjusting tamoxifen doses based on individual metabolism can reduce the number of breast cancer patients who stop treatment early due to side effects. About 1,100 premenopausal or perimenopausal women with hormone-sensitive breast cancer will receive either standard or personalized dosing. The goal is to improve adherence and survival outcomes.

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Conditions

The condition(s) this trial relates to.

As listed by the trial registrant

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

Contacts and locations

Locations

  • Capio S:t Görans Sjukhus

    NOT_YET_RECRUITING

    Stockholm, 112 81, Sweden

  • S:a Älvsborgs Sjukhus

    NOT_YET_RECRUITING

    Borås, 501 82, Sweden

  • Skaraborgs Sjukhus

    RECRUITING

    Skövde, 549 49, Sweden

  • Södersjukhuset, Onkologiska kliniken

    RECRUITING

    Stockholm, 118 61, Sweden

More trials for these conditions

Other studies related to the condition(s) this trial covers.