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Can pancreatic Cancer's inflammatory footprint be stopped?

NCT ID NCT07765316

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting This study
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Aug 14, 2026 · Last updated Aug 18, 2026 · Updated 2 times

Summary

This observational study looks at how pancreatic cancer changes immune cells in the blood. Researchers will compare blood samples from 50 people with newly diagnosed, untreated pancreatic cancer to 50 age-matched people with a non-cancerous pancreatic condition. They aim to identify specific immune cell changes driven by tumor-related inflammation, which could reveal new targets for future treatments. Participants with cancer will be followed for 12 months to see if these immune changes relate to their clinical outcomes.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

What this could lead to
If successful, this could identify new drug targets to block cancer-related inflammation and potentially improve future treatments for pancreatic cancer.
What could go wrong
This is an observational study, so it won't test any treatment directly. Findings may not lead to immediate therapies, and results might not apply to all patients.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Participants

About 100 people

The number the study aims to enrol. It can still change while the study runs.

Expected to start

Sep 2026

An estimate. Start dates often move.

Expected to finish

Dec 2029

An estimate. End dates often move.

Lead sponsor

Other sponsor

The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Who is studied

The study population will include adults with newly diagnosed, non-metastatic, treatment-naïve pancreatic ductal adenocarcinoma (PDAC) evaluated at the Pancreatic Surgery Unit of IRCCS Ospedale San Raffaele, and age-matched control patients. Controls will be recruited among patients with intraductal papillary mucinous neoplasm (IPMN) under surveillance at the Pancreatic Cystic Lesion outpatient clinic, with no evidence of pancreatic malignancy at enrollment. Control patients will be selected to match the age of PDAC patients within ±5 years whenever feasible. The study will include 50 PDAC patients and 50 age-matched controls

Ages

18 years and older

Sex

Anyone

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria * For all participants: * Age ≥18 years. * Ability and willingness to autonomously provide written informed consent. * For the PDAC cohort: * Clinical diagnosis of non-metastatic pancreatic ductal adenocarcinoma (PDAC). * Treatment-naïve status at the time of blood collection, with no prior chemotherapy, radiotherapy, or immunotherapy for PDAC. * Newly diagnosed non-metastatic pancreatic cancer eligible for multimodal treatment. * Candidate for standard clinical management at IRCCS Ospedale San Raffaele. * For the age-matched control cohort: * Patient followed at the Pancreatic Cystic Lesion outpatient clinic of IRCCS Ospedale San Raffaele. * Diagnosis of intraductal papillary mucinous neoplasm (IPMN) under surveillance, with no evidence of pancreatic malignancy at the time of enrollment. * Age within ±5 years of the corresponding PDAC cohort to allow age-matched comparator analyses. * Exclusion Criteria * For all participants: * Inability to autonomously provide informed consent. * For the PDAC cohort: * Failure to meet the inclusion criteria for the PDAC cohort. * Presence of severe comorbidities that, in the investigator's opinion, may interfere with study participation or interpretation of study results. * Previous systemic anti-cancer treatment for PDAC. * Use of anti-inflammatory drugs, including NSAIDs or immunomodulators. * Events or conditions affecting inflammatory parameters, including acute inflammatory or infectious events such as cholangitis, jaundice, or recent invasive procedures. * Hematologic diseases. * Clinically significant hematological abnormalities that may interfere with immune profiling analyses, as assessed by the investigator. * For the age-matched control cohort: * Any acute or chronic inflammatory condition or ongoing infection. * Any history of cancer or immunological disorders.

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Conditions

The condition(s) this trial relates to.

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

How to take part

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  1. The official record

    ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.

    Open the record ↗

  2. A doctor treating you

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