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NCT07421479Active, not recruiting

Patient-Derived Breast Cancer Organoids for Therapeutic Extracellular Vesicle Isolation (PDO-Mercurial01)

Prospective Single-center Study for the Generation of Organoids From Patients With Breast Carcinoma for Use in Extracellular Vesicle Isolation

Source: ClinicalTrials.gov · Last updated 19 Feb 2026

Brief summary (registry, in English)

The aim of this study is to establish organoid cultures, which are three-dimensional in vitro tumor models capable of supporting the long-term ex vivo growth of tumor cells derived from patients with breast carcinoma. These organoids will be used for the isolation of extracellular vesicles (EVs), which are naturally released by cells and have the ability to selectively recognize tumor tissue. Due to these properties, EVs represent promising vectors for the targeted delivery of diagnostic agents, with potential applications in fluorescence-guided surgery.

Status (registry)
Active, not recruiting
Study type
Observational
Enrollment
50 (estimated)
First submitted
12 Feb 2026
Start date
1 Jan 2025
Primary completion date
28 Oct 2027
Lead sponsor
Istituti Clinici Scientifici Maugeri SpA
NCT number
NCT07421479

What you commit to

  • Study type: Observational
  • Planned participants: 50
  • From 1 Jan 2025 to the primary completion date, 28 Oct 2027
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other

  • Patients without a proven cyto-histological diagnosis of breast carcinoma;
  • Subjects affected by other solid tumors besides the breast lesion.

Who the study is looking for

  • Female subjects;
  • Confirmed diagnosis of breast heteroplasia
  • Age \>= 18 years;
  • Patients willing to follow the usual oncological follow-up;
  • Patients with de novo metastatic disease (M+), receiving primary chemotherapy, if candidates for primary tumor biopsy;
  • Subjects who agree to participate in the study by signing and dating the Informed Consent form.

Age in the registry: 18 years to - · Sex: Female · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Istituti Clinici Scientifici Maugeri
Coordinator of this site? Confirm its status
PaviaItalyUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.