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
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Capio S:t Görans Sjukhus
NOT_YET_RECRUITINGStockholm, 112 81, Sweden
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S:a Älvsborgs Sjukhus
NOT_YET_RECRUITINGBorås, 501 82, Sweden
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Skaraborgs Sjukhus
RECRUITINGSkövde, 549 49, Sweden
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Södersjukhuset, Onkologiska kliniken
RECRUITINGStockholm, 118 61, Sweden
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Other studies related to the condition(s) this trial covers.
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