CI

At a glance

ClinicalIndex Comparison Record
Phase 2Active· 290 target
Drug / intervention
Tamoxifen Citratedrug
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT03917082
NCT03917082Phase 2ActiveMonitorUpdated 36mo ago · Completion was 2mo ago
Slow Enrollment

LA LEAST- Luminal A, Limited Endocrine Adjuvant Systemic Therapy. A Trial of Abbreviated Hormone Therapy for Low Risk Hormone Receptor Positive, HER2 Negative Early Breast Cancer

British Columbia Cancer Agency·interventional·Posted Apr 16, 2019·Updated Jun 15, 2023

In Brief

A Phase 2 clinical trial evaluating Tamoxifen Citrate for Breast Cancer Female and Hormone Receptor Positive Tumor. Active but no longer recruiting, targeting 290 participants across 1 site.

Signals

Enrolling slower than its timeline implies

Detailed Summary

Phase II trial of 2 years of standard adjuvant endocrine therapy after low risk hormone receptor positive, HER2 negative, node negative breast cancer in women older than 50 at diagnosis. The study hypothesis is that reducing adjuvant endocrine therapy from 5 to 2 years in a population with low risk of breast cancer; as determined by histopathologic criteria and confirmed by low risk genomic analysis using Prosigna®; will be safe and acceptable to this population, and will not compromise the expected excellent breast cancer specific outcomes for this population.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesCanada

Timeline

Phase 2Active
2020202120222023202420252026202720282029
First PostedApr 16, 2019
Enrollment StartSep 23, 2019
Primary CompletionMay 1, 2026
Study CompletionMay 1, 2029
TodayJul 2, 2026
Enrollment to primary: 6.6 yearsPosted 7.2 years ago

Interventions

Tamoxifen Citratedrug

current standard of care is 5 years endocrine therapy after early breast cancer. Intervention will test if 2 years is adequate for population with low recurrence risk based on genomic tissue based test