Actively Recruiting

Phase 2
Age: 18Years +
All Genders
NCT04683315

PurIST Classification-Guided Adaptive Neoadjuvant Chemotherapy by RNA Expression Profiling of EUS Aspiration Samples

Led by Medical College of Wisconsin · Updated on 2026-03-05

84

Participants Needed

2

Research Sites

404 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

This is an open-label, phase II study in patients with resectable and borderline resectable pancreatic cancer.

CONDITIONS

Official Title

PurIST Classification-Guided Adaptive Neoadjuvant Chemotherapy by RNA Expression Profiling of EUS Aspiration Samples

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Have suspicion of pancreatic adenocarcinoma and plan for endoscopic biopsy or agree to additional biopsy for research
  • Be 18 years of age or older
  • Able to provide informed consent or have a legally authorized representative
  • Histologically confirmed pancreatic adenocarcinoma
  • Eastern Cooperative Group (ECOG) performance status less than 2
  • Clinical stage consistent with resectable or borderline resectable pancreatic adenocarcinoma based on CT or MRI
  • Adequate organ and bone marrow function, including specified leukocyte, neutrophil, hemoglobin, platelet counts, creatinine clearance, and liver enzyme levels
  • Female patients must be postmenopausal, surgically sterile, or have a negative pregnancy test and use contraception before and during study treatment
  • Male patients must be surgically sterile or use barrier contraception during and after study treatment
Not Eligible

You will not qualify if you...

  • Received chemotherapy and/or radiation within three years prior to enrollment
  • History of another malignancy within three years except certain cured skin, cervical, or prostate cancers
  • Uncontrolled serious comorbidities including infections, heart failure, unstable angina, arrhythmias, psychiatric illness, or excessive obesity (BMI >55)
  • Known HIV, hepatitis B, or hepatitis C infection
  • Pregnant or breastfeeding or childbearing potential without contraception four weeks prior to treatment

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 2 locations

1

HonorHealth Medical Group

Scottsdale, Arizona, United States, 85258-4566

Actively Recruiting

2

Froedtert & the Medical College of Wisconsin

Milwaukee, Wisconsin, United States, 53226

Actively Recruiting

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Research Team

M

Medical College of Wisconsin Cancer Center Clinical Trials Office

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NON_RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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