New combo therapy aims to tackle tough pancreatic tumors
NCT ID NCT06217666
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This early-stage study tests if combining radiation therapy with an experimental immunotherapy called PCX12 is safe for people with locally advanced pancreatic cancer. About 24 participants who have already had chemotherapy will receive radiation followed by injections of PCX12 directly into the tumor. The main goal is to find the safest dose and check for side effects.
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Study facts
What this study's own registry entry says, in plain language.
- Phase
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Phase 1
The first testing in people. Mainly checks safety and dose, usually in a small group.
- Participants
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About 24 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Dec 2026
An estimate. Start dates often move.
- Expected to finish
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Dec 2029
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.
- 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.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Patient with pathologically proven diagnosis of adenocarcinoma of the pancreas * After chemotherapy, tumor is determined to be either locally advanced or unresectable by hepatobiliary surgeon; or tumor is considered potentially resectable but subject does not proceed with surgical resection for any reason * Have completed first line chemotherapy without progression or non-regional metastases * Tumor is radiographically evident on CT scan after chemotherapy * Tumor is anatomically amenable to SBRT, e.g. does not directly invade the stomach or bowel * Tumor is amenable to intra-tumor injection under endoscopic ultrasound guidance * ECOG performance status 0-2 * Patients with childbearing potential must demonstrate a negative urine or serum pregnancy test * Male or female subjects, aged at least 18 years; Female subjects of childbearing potential may participate if adequate contraception is used during, and for at least the three months after study completion; Male subjects with partners of childbearing potential may participate in the study if they had a vasectomy at least 6 months prior to randomization or if adequate contraception is used during, and for at least the three months after study completion; Adequate contraception is defined as resulting in a failure rate of less than 1% per year * Patient must be able to understand and willingly sign study specific informed consent prior to study entry * Anticipated life expectancy ≥ 12 weeks * Patients aged at least 18 years of age Exclusion Criteria: * Progression of disease or metastatic disease after first line systemic therapy * Prior radiation treatment or surgical resection of any pancreatic malignancy * Inability to tolerate SBRT, Endoscopic ultrasound or IL-12 Injection procedure * Lack of radiographically evident disease after first line chemotherapy * Severe, active comorbidity that shortens the patient's life expectancy to less than 12 weeks * History of past malignancy * Patient who is pregnant and/or breastfeeding * Inability to comply with other required protocol procedures including required biopsies
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Genom att skicka in godkänner du våra Användarvillkor
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 study's own enquiry address
This study publishes an address for enquiries. See it below .
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The places running it
1 site. The list below names each one and where it is.
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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
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Contacts and locations
Show contact details
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Genom att skicka in godkänner du våra Användarvillkor
Study contacts
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Contact
Email: •••••@•••••
Locations
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University of Rochester
Rochester, New York, 14642, United States
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Other studies related to the condition(s) this trial covers.
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