PREDICT-RD: ctDNA Surveillance in TNBC With Residual Disease

Recruiting Phase 2 Interventional Study
Breast Cancer Residual Disease Triple Negative Breast Cancer (TNBC) Stage II/III
No Placebo Group Every participant receives an active treatment — no one gets a placebo. Prior Safety Data This treatment has already been tested in at least one earlier human trial.
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At a Glance
Age
18 and older
Sex
Any
Trial phase
Phase 2
Study type
Interventional
Purpose
Treatment
Participants needed
78 (estimated)
Sponsor
UNC Lineberger Comprehensive Cancer Center · Other
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About This Trial
This is a Phase II, interventional, prospective, single-arm, multi-center study that will enroll patients with stage II/III triple negative breast cancer (TNBC) who have residual cancer burden (RCB) II/III after conventional neoadjuvant chemo-immunotherapy followed by surgery. Technological advances in ctDNA assays have improved both the sensitivity and reliability of molecular residual disease (M…
Trial Locations
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Eligibility Criteria
Inclusion Criteria: Written informed consent was obtained to participate in the study, and HIPAA authorization for the release of personal health information. * Participant is willing and able to comply with study procedures based on the judgment of the investigator. * Age ≥ 18 years at the time o…
Contacts

Taylor Pierce

(919) 445-4827

Taylor_Pierce@med.unc.edu

CONTACT