Dose-determining and Dose-confirmatory Study to Investigate the Optimal Dose of Tamoxifen in Breast Cancer Patients According to Genotype Status of TCF20 rs932376

PHASE1Active, not recruitingINTERVENTIONAL
Enrollment

75

Participants

Timeline

Start Date

December 23, 2020

Primary Completion Date

November 30, 2025

Study Completion Date

November 30, 2025

Conditions
Breast Cancer
Interventions
DRUG

Tamoxifen

Patients taking 20mg tamoxifen will receive dose increments of 10mg every 8 weeks until endoxin threshold of \>30nM or the maximum dose of 40mg/day is reached. The escalated dose will be taken for 1 year before reverting back to 20mg.

DRUG

Tamoxifen

Patients will take tamoxifen at the ascribed genotype-determined dose as determined in the dose-determination phase.

Trial Locations (1)

169610

National Cancer Centre, Singapore

All Listed Sponsors
collaborator

National Medical Research Council (NMRC), Singapore

OTHER_GOV

lead

National Cancer Centre, Singapore

OTHER

NCT04961632 - Dose-determining and Dose-confirmatory Study to Investigate the Optimal Dose of Tamoxifen in Breast Cancer Patients According to Genotype Status of TCF20 rs932376 | Biotech Hunter | Biotech Hunter