Pfizer COVID-19 vaccine appointments are available to our patients. Sign up for Connect today to schedule your vaccination.

A012301- LoTam: A Randomized, Phase III Clinical Trial of Low-Dose Tamoxifen for Selected Patients with Molecular Low-Risk Early-Stage Breast Cancer

Clinical Trial Details

The purpose of this study is to compare the usual treatment with hormonal therapy medications to treatment with low-dose tamoxifen for patients with molecular low-risk early-stage breast cancer.   

This study has 2 study groups. Participants will be randomized by a computer to assign them to one of the study groups.

Group 1 will take the usual drugs used to treat this type of cancer, either anastrozole, letrozole, exemestane, or tamoxifen, 20 mg/day orally for a total of 5 years. Group 2 will take tamoxifen at a lower dose orally for a total of 5 years.

All treatments in this study are approved by the U.S. Food and Drug Administration (FDA).

Study participation also includes study visits and follow-up 6 months after starting the study and then every year for the next 10 years.

Key Eligibility: 
  1. Open to women above the age of 18 who have been diagnosed with invasive breast cancer.
  2. Patients must not have a history of ipsilateral or contralateral invasive breast cancer. 

 Detailed eligibility will be reviewed when contacting the study team.

Study contact by location

Upper East Side - Manhattan

Contact(s)

Daniella Topol, RN
212-746-4154
dat7032@med.cornell.edu

Queens

Contact(s)

Roan Raymundo
929-470-9507
ror7059@med.cornell.edu

Brooklyn

Contact(s)

Charlotte Fong
718-660-1716
ccf4001@med.cornell.edu

Primary Investigator(s)

Protocol ID(s)

Weill Cornell Medicine IRB #:

2509029281

ClinicalTrials.gov:

NCT06671912

Sponsor:

A012301

Status

Open to Enrollment

Age Group

Adult

Sponsor

Disease