New study tests if tumor genes and organoids can outsmart pancreatic cancer
NCT ID NCT06615830
First seen Jun 24, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This observational study will enroll 185 people with metastatic pancreatic cancer to see if analyzing tumor genes and lab-grown organoids can predict which standard chemotherapy regimens work best. Researchers will compare predicted drug sensitivity to actual patient outcomes. The tests are experimental and not used to guide treatment decisions.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Transcriptome-based OncoTreat/OncoTarget testing and patient-derived organoids
- What this could lead to
- If successful, this could show that combining genetic analysis with organoid testing helps predict effective treatments for pancreatic cancer, paving the way for more personalized therapy.
- What could go wrong
- This is an observational study, not a treatment trial. The tests are experimental and not yet proven to improve outcomes. Results may 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
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About 185 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Jun 2026
An estimate. Start dates often move.
- Expected to finish
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Jan 2031
An estimate. End dates often move.
- Lead sponsor
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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
All patients with the diagnosis of metastatic adenocarcinoma of the pancreas can be enrolled provided the above mentioned criteria apply. The patients can either be therapy-naive or pretreated.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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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 Hide 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: * Informed Consent as documented by signature * Patients older than 18 years * Patients with metastatic pancreatic ductal adenocarcinoma * At least one lesion amenable for surgical excisional biopsy * ECOG Performance status 0-2 * Radiologically measurable disease * Life expectancy \> 3 months * Absolute leucocyte count \>1.5 G/l, platelets \>100 G/l * Serum creatinine \<1.5 times of the upper limit of normal or Clearance \>50ml/min (according to the CKD-EPI formula) Exclusion criteria: * Known allergies or intolerance to one or more compounds present in one of the first line or second line regimens * Concomitant need for full anticoagulation that cannot be interrupted or bridged prior to tissue biopsy * ECOG PS \>2 * Heart failure (NYHA class III-IV) * Severe or uncontrolled concurrent illness * Active viral infection from HIV, HBV or HCV, even if under antiretroviral treatment * Myocardial infarction within the previous 6 months * Patients who are pregnant or breastfeeding
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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
Only the study team decides who joins. These are the ways to reach them.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
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Other studies related to the condition(s) this trial covers.
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