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NCT07542041Recruiting

Artidis Nanomechanical Signature Profiling of Pancreatic Cancer Specimens

Artidis Nanomechanical Signature Profiling of Pancreatic Cancer Specimens (ANoPs)

Source: ClinicalTrials.gov · Last updated 18 Aug 2026

Brief summary (registry, in English)

The goal of this clinical study is to evaluate whether the NEO-Match® test, based on ARTIDIS nanomechanical profiling technology, can help predict treatment outcomes and improve clinical decision-making in patients with suspected pancreatic cancer undergoing biopsy. The main questions this study aims to answer are: * Can the NEO-Match® test predict how patients respond to neoadjuvant (pre-surgical) treatment for pancreatic cancer? * How well does the NEO-Match® test detect malignant pancreatic lesions compared to standard histopathological assessment? This is a prospective, single-arm study. Researchers will compare results from the NEO-Match® test with standard clinical outcomes, imaging findings, and pathology results to evaluate its predictive and diagnostic performance. Participants will: * Undergo a standard-of-care pancreatic biopsy or surgical procedure * Provide an additional biopsy sample for research analysis using the ARTIDIS ART-1 device * Continue to receive standard treatment and care, which is not influenced by the study * Have clinical data, imaging results, and treatment outcomes collected * Be followed every 3 months for up to 2 years The study does not involve experimental treatment or changes to standard medical care. The information collected may help improve future diagnosis, prognosis, and treatment selection for patients with pancreatic cancer.

Status (registry)
Recruiting
Study type
Interventional
Enrollment
200 (estimated)
First submitted
14 Apr 2026
Start date
17 Apr 2026
Primary completion date
May 2028
Lead sponsor
ARTIDIS AG
NCT number
NCT07542041

What you commit to

  • Study type: Interventional
  • Planned participants: 200
  • From 17 Apr 2026 to the primary completion date, May 2028
  • 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 illness

  • Any condition that, in the opinion of the investigator, makes the subject unsuitable for participation in the study

Who the study is looking for

  • Age ≥ 18 years
  • Ability to understand and willingness to sign a written informed consent form
  • Clinical indication for fine needle biopsy (FNB) of a suspicious pancreatic lesion accessible for biopsy

Age in the registry: 18 years to - · Sex: All · 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
Moffitt Cancer Center
Coordinator of this site? Confirm its status
TampaUnited StatesRecruiting

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