Development of Patient Derived Xenografts (PDX) in Patients With Breast Cancer
Part of paid clinical trials in Rochester, Minnesota.
- Sponsor
- Mayo Clinic
- Study ID
- NCT04703244
- Status
- Recruiting
Conditions
- Breast Cancer
- Residual
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- chemotherapy or endocrine therapy for breast cancer — PROCEDURECollect blood and leftover surgical tissue from patients with breast cancer remaining after chemotherapy or endocrine therapy is completed.
Study Details
Breast cancer patients who undergo neoadjuvant systemic therapy and have residual breast cancer identified at the time of surgery exhibit a high (\>50%) risk of future life-threatening recurrences and death.
Key Dates
- Start date
- Jan 13, 2021
- Status verified
- Feb 2026
- Primary completion
- Jan 15, 2041
- Completion
- Jan 15, 2042
Study Design
- Enrollment
- 999 participants (estimated)
Primary Outcome Measure
Generate patient derived xenografts (PDX) and organoids from breast cancer patients with residual disease after neoadjuvant therapy [ Time Frame: Up to 12 months until death or a maximum of 20 years post registration ]
Central Contacts
- Clinical Trials Referral Office855-776-0015
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| Mayo Clinic | Rochester | Minnesota | 55905 | Judy C. Boughey, M.D. (PRINCIPAL_INVESTIGATOR) Matthew P. Goetz, M.D. (PRINCIPAL_INVESTIGATOR) |
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