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Johns Hopkins Breast Cancer Program Longitudinal Repository

Johns Hopkins Breast Cancer Program Longitudinal Repository

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01937039
Enrollment
810
Registered
2013-09-09
Start date
2009-04-01
Completion date
2030-01-01
Last updated
2026-05-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Benign Breast Disease, Breast Cancer

Brief summary

The Breast Cancer Program Longitudinal Repository (BCPLR) is being established to fulfill the research mission of the Breast Cancer Program at Johns Hopkins and to serve investigators affiliated with it - to develop a repository of specimens with corresponding characteristics from patients seen in the breast care and cancer clinics.

Detailed description

This research is being done to collect samples for future use that we may learn more about cancer by studying cells in blood and tissue collected from people with breast cancer as well as from volunteers without breast cancer. Our goal is to make these available for research to help to learn how cancer develops and how it may be treated.

Interventions

PROCEDURESample collection

Blood, tissue, urine, and other samples may be collected

Sponsors

Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins
Lead SponsorOTHER
Susan G. Komen Breast Cancer Foundation
CollaboratorOTHER

Study design

Observational model
OTHER
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Male or female * 18 years of age or older * Participants meet one of the following categories: have a known diagnosis of breast cancer receiving a breast cancer evaluation and/or treatment; have benign breast disease receiving a diagnostic procedure and/or evaluation; or, have no known diagnosis of breast disease or abnormality and is undergoing routine screening or diagnostic breast imaging procedures and/or other clinical evaluation.

Exclusion criteria

* N/A

Design outcomes

Primary

MeasureTime frameDescription
Repository development20 yearsTo develop a repository of specimens with corresponding characteristics - demographic and clinical information - from patients seen in the breast care and cancer clinics

Countries

United States

Contacts

STUDY_CHAIRAntonio C. Wolff, MD

Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: May 15, 2026