Status:

RECRUITING

EXoPERT EMERALD Clinical Study

Lead Sponsor:

EXoPERT

Collaborating Sponsors:

MCRA

Conditions:

Breast Cancer

Colon Cancer

Eligibility:

All Genders

45+ years

Brief Summary

Invitro diagnostic test for multiple cancer diagnosis for patients with early-stage cancers by analyzing surface-enhanced Ramen spectroscopy (SERS) profiles of extracellular vesicles (EV) using artifi...

Detailed Description

An in vitro diagnostic medical device and system that provides information on the presence of lung, ovarian, breast, pancreas and colorectal cancers based on a deep learning analysis for Raman spectro...

Eligibility Criteria

Inclusion

  • Subjects aged 45 years or older with a biopsy-proven lung, breast, colorectal, pancreatic, or ovarian cancer, as their primary cancer, but whose blood was collected prior to any systemic or definitive therapy for the cancer.
  • Subjects who are willing and able to provide written informed consent.
  • Subjects who are willing and able to comply with the study requirements.

Exclusion

  • Any history of cancer diagnosed and treated within 5 years prior to the date of consent.
  • Subjects with a history of previous cancer treatment via hormonal cancer treatment, chemotherapy, radiotherapy within the past 6 months.
  • Subjects who have evidence of active febrile infection prior to blood draw.
  • Subjects who have any history of an allogeneic bone marrow, stem cell transplant, or solid organ transplant.
  • Subjects who have been diagnosed with dementia or neurological disease.
  • Subjects who are pregnant or breastfeeding women.
  • Subjects who have consented and have undergone treatment in any other clinical trials within the past 6 months.
  • Subjects who are currently in active treatment for drug abuse.
  • Subjects who have received any treatment related to lung, breast, colorectal, pancreatic, or ovarian nodules, such as hormones prior to entering the study.
  • Unsuitable sample for testing due to contamination, hemolysis, etc.

Key Trial Info

Start Date :

May 9 2025

Trial Type :

OBSERVATIONAL

Allocation :

ESTIMATED

End Date :

June 30 2026

Estimated Enrollment :

1400 Patients enrolled

Trial Details

Trial ID

NCT07186296

Start Date

May 9 2025

End Date

June 30 2026

Last Update

September 22 2025

Active Locations (2)

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Page 1 of 1 (2 locations)

1

KCTL

Louisville, Kentucky, United States, 40202

2

John Hopkins University

Baltimore, Maryland, United States, 21218