RecruitingPhase 2NCT05941520

Acolbifene Versus Low Dose Tamoxifen for the Prevention of Breast Cancer in Premenopausal Women at High Risk for Development of Breast Cancer

Phase IIA Trial of Acolbifene (20 mg) vs Low Dose Tamoxifen (5 mg) in Pre-menopausal Women at High Risk for Development of Breast Cancer


Sponsor

National Cancer Institute (NCI)

Enrollment

80 participants

Start Date

Aug 23, 2024

Study Type

INTERVENTIONAL

Conditions

Summary

This phase IIA trial compares the effect of acolbifene versus low dose tamoxifen in preventing breast cancer in premenopausal women at high risk for developing breast cancer. The usual approach for patients at increased risk for breast cancer is to undergo yearly breast magnetic resonance imaging or ultrasound in addition to yearly mammogram. Premenopausal women at very high lifetime risk for breast cancer (greater than 50%) can consider preventive removal (mastectomy) of both breasts. Premenopausal women age 35 or older with a prior diagnosis of atypical hyperplasia, lobular carcinoma in situ, or an estimated 10-year risk of greater than or equal to 3% or estimated 10-year risk of greater than or equal to 2-5 times that of the average woman (depending on age) may be advised to consider five years of standard dose tamoxifen. Standard dose tamoxifen is four times the dose used in this study. Estrogen can cause the development and growth of breast cancer cells. Acolbifene and tamoxifen blocks the use of estrogen by breast cells. This study may help researchers measure the effects of acolbifene and low dose tamoxifen on markers of breast cancer risk in mammogram imaging, breast tissue, and in blood samples.


Eligibility

Sex: FEMALEMin Age: 35 Years

Plain Language Summary

Simplified for easier understanding

This study is comparing two medications — acolbifene and low-dose tamoxifen — to prevent breast cancer in premenopausal women who are at high risk, to see which is more effective and has fewer side effects. **You may be eligible if...** - You are 35 years old or older - You are premenopausal (still having regular periods, roughly every 21–35 days) - You are at high risk for developing breast cancer (based on personal or family history, genetic factors, or abnormal biopsy findings) - You are willing to use contraception if you are of childbearing age **You may NOT be eligible if...** - You have already been diagnosed with invasive breast cancer - You have a history of blood clots (deep vein thrombosis or pulmonary embolism) - You are currently pregnant, breastfeeding, or trying to conceive - You are already taking hormonal contraceptives or hormone therapy that would interact with the study medications - You have had a hysterectomy or are postmenopausal Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

Interested in this trial?

Get notified about updates and connect with the research team.

Interventions

DRUGAcolbifene Hydrochloride

Given PO

PROCEDUREBiospecimen Collection

Undergo collection of blood

PROCEDUREMammography

Undergo 3D mammography

OTHERQuestionnaire Administration

Ancillary studies

PROCEDURERandom Periareolar Fine-Needle Aspiration

Undergo RPFNA

DRUGTamoxifen

Given PO


Locations(4)

City of Hope Comprehensive Cancer Center

Duarte, California, United States

Northwestern University

Chicago, Illinois, United States

University of Kansas Cancer Center

Kansas City, Kansas, United States

Ohio State University Comprehensive Cancer Center

Columbus, Ohio, United States

View Full Details on ClinicalTrials.gov

For the most up-to-date information, visit the official listing.

Visit

NCT05941520


Related Trials