Circulating Tumor DNA (NCT06923527)
A Single Arm Phase II Trial of Circulating Tumor DNA-guided Adjuvant Therapy With Elacestrant in Adults With Hormone Receptor Positive HER2 Negative Breast Cancers at Risk for Late Recurrence (CATE)
๐ฉบ Plain-English Summary (8th-Grade Level)
This is a single-arm, phase II study examining elacestrant in the adjuvant treatment of patients with ER+ breast cancer who test positive for circulating tumor DNA (ctDNA) during the screening period of the trial. Our trial will proceed in three separate phases: screening, treatment, and follow-up.
Who can join: Review the eligibility criteria below.
Location: Yale University โ New Haven, Connecticut
Age range: 18 Years
๐งช Interventions in This Study
๐ "Do I Qualify?" โ 1-Minute Self Screener
Instant ChecklistFull eligibility criteria are available on the official NIH protocol. View the criteria โ
๐ All Participating Trial Locations (7 Sites)
- Yale University โ New Haven, Connecticut
- Lombardi Comprehensive Cancer Center at Georgetown University Medical Center โ Washington D.C., District of Columbia
- Sidney Kimmel Comprehensive Cancer Center at John Hopkins โ Baltimore, Maryland
- Dana-Farber Cancer Institute โ Boston, Massachusetts
- Montefiore Einstein Comprehensive Cancer Center โ The Bronx, New York
- UPMC Hillman Cancer Center โ Pittsburgh, Pennsylvania
- The University of Texas MD Anderson Cancer Center โ Houston, Texas
๐ Contact the Study Coordinator
Phone: (773) 369-6904
Email: laura.kane@yale.edu
Coordinator details come directly from the registered NIH protocol. Confirm the study is still recruiting before traveling.
๐ฐ Cost, Insurance & Patient Rights
- 100% Free Items: The investigational treatment and protocol-required procedures are supplied at zero cost by the sponsor.
- Routine Patient Care: Under federal law (ACA ยง 2709) and many state statutes, routine care costs are covered during participation.
- Voluntary Participation: You may withdraw at any time without affecting your standard medical care.
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Explore by condition: All ER+ Breast Cancer clinical trials
๐ก How to Participate
- Check the checklist above to see if you may qualify.
- Contact the study coordinator using the phone/email above.
- Ask about the visit schedule, what is covered at no cost, and any travel support.
- Confirm with your own doctor before making a decision.