NCT06388967

Brief Summary

This study aims to prospective validate an exosome-based miRNA signature for noninvasive and early detection of pancreatic ductal adenocarcinoma.

Trial Health

80
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
2,000

participants targeted

Target at P75+ for all trials

Timeline
2mo left

Started Mar 2023

Typical duration for all trials

Geographic Reach
3 countries

11 active sites

Status
recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Progress97%
Mar 2023Jun 2026

Study Start

First participant enrolled

March 15, 2023

Completed
1.1 years until next milestone

First Submitted

Initial submission to the registry

April 19, 2024

Completed
10 days until next milestone

First Posted

Study publicly available on registry

April 29, 2024

Completed
2.1 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

June 18, 2026

Expected
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

June 18, 2026

Last Updated

December 19, 2025

Status Verified

December 1, 2025

Enrollment Period

3.3 years

First QC Date

April 19, 2024

Last Update Submit

December 17, 2025

Conditions

Keywords

Micro RNAExosomeCell freeEarly detectionScreening

Outcome Measures

Primary Outcomes (1)

  • Sensitivity

    True positive rate: the probability of a positive test result, conditioned on the individual truly being positive

    Through study completion, an average of 1 year

Secondary Outcomes (2)

  • Specificity

    Through study completion, an average of 1 year

  • Accuracy

    Through study completion, an average of 1 year

Study Arms (4)

Patients with Pancreatic Cancer Ductal Adenocarcinoma (Training)

Individuals diagnosed with pancreatic ductal adenocarcinoma

Diagnostic Test: PANcreatic cancer Exosome Early detectiON (PANXEON)

Individuals without Pancreatic Cancer Ductal Adenocarcinoma (Training)

Individuals without pancreatic ductal adenocarcinoma

Diagnostic Test: PANcreatic cancer Exosome Early detectiON (PANXEON)

Patients with Pancreatic Cancer Ductal Adenocarcinoma (Validation)

Individuals diagnosed with pancreatic ductal adenocarcinoma

Diagnostic Test: PANcreatic cancer Exosome Early detectiON (PANXEON)

Individuals without Pancreatic Cancer Ductal Adenocarcinoma (Validation)

Individuals without pancreatic ductal adenocarcinoma

Diagnostic Test: PANcreatic cancer Exosome Early detectiON (PANXEON)

Interventions

This test will utilize quantitative reverse transcriptase polymerase chain reaction (qRT-PCR) to quantify the expression levels of 5 cell-free and 8 exosome-miRNAs in plasma samples obtained from patients with pancreatic ductal adenocarcinoma and from individuals without it

Also known as: PANXEON (PANcreatic cancer Exosome Early detectiON)
Individuals without Pancreatic Cancer Ductal Adenocarcinoma (Training)Individuals without Pancreatic Cancer Ductal Adenocarcinoma (Validation)Patients with Pancreatic Cancer Ductal Adenocarcinoma (Training)Patients with Pancreatic Cancer Ductal Adenocarcinoma (Validation)

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

Independent cohorts of individuals with and without pancreatic cancer (cases and controls, respectively)

You may qualify if:

  • Histological diagnosis of pancreatic ductal adenocarcinoma, stages I-IV (TNM classification, 8th edition)
  • Received standard diagnostic and staging procedures as per local guidelines, and at least one sample was drawn before receiving any curative-intent treatment.
  • Imaging- or endoscopy-based proof of lack of pancreatic ductal adenocarcinoma at the time of sampling (Non-disease controls)

You may not qualify if:

  • Lack of written informed consent.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (11)

Translational Genomics Research Institute

Phoenix, Arizona, 85004, United States

RECRUITING

Honorhealth

Scottsdale, Arizona, 85258, United States

RECRUITING

City of Hope Medical Center

Monrovia, California, 91016, United States

RECRUITING

Hoag Center

Newport Beach, California, 92663, United States

RECRUITING

OSF HealthCare

Peoria, Illinois, 61637, United States

RECRUITING

Ochsner Medical Center

Jefferson, Louisiana, 70121, United States

RECRUITING

Atlantic Health System

Morristown, New Jersey, 07960, United States

RECRUITING

Piedmont Medical Center

Rock Hill, South Carolina, 29732, United States

RECRUITING

Medical College of Wisconsin

Milwaukee, Wisconsin, 53226, United States

RECRUITING

Nagoya University

Nagoya, Japan

RECRUITING

Asan Medical Center

Seoul, South Korea

RECRUITING

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Biospecimen

Retention: SAMPLES WITHOUT DNA

Serum

MeSH Terms

Conditions

Pancreatic NeoplasmsPancreatic cancer, adult

Condition Hierarchy (Ancestors)

Digestive System NeoplasmsNeoplasms by SiteNeoplasmsEndocrine Gland NeoplasmsDigestive System DiseasesPancreatic DiseasesEndocrine System Diseases

Study Officials

  • Ajay Goel, PhD

    City of Hope Medical Center

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Ajay Goel, PhD

CONTACT

Study Design

Study Type
observational
Observational Model
CASE CONTROL
Time Perspective
PROSPECTIVE
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

April 19, 2024

First Posted

April 29, 2024

Study Start

March 15, 2023

Primary Completion (Estimated)

June 18, 2026

Study Completion (Estimated)

June 18, 2026

Last Updated

December 19, 2025

Record last verified: 2025-12

Locations