Pancreatic Cancer Trial, Recruiting NCT06984562 Sponsor: Fox Chase Cancer Center Condition: Pancreatic Cancer
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Pancreatic Cancer Trial, Recruiting

NCT06984562
Recruiting Not Applicable

Who may be able to join

AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI

Who might be able to join this trial:

  • People who have been diagnosed with pancreatic ductal adenocarcinoma (a specific type of pancreatic cancer), confirmed by a tissue or cell sample test.
  • People whose pancreatic cancer has been determined to be locally advanced and cannot be removed by surgery, based on specific reasons such as the tumor being too close to or wrapped around major blood vessels or the aorta, or surgery being considered too risky for that person.
  • People whose case has been reviewed by a team of specialists, including a pancreatic surgeon, who have confirmed the cancer cannot be surgically removed.
  • People who have either already received initial chemotherapy before radiation treatment, or who have been assessed by an oncologist as not being suitable for that initial chemotherapy — and where chemotherapy was received, the last dose must have been given at least 2 weeks before the radiation treatment begins (for those in the dose escalation part of the trial).
  • People who are reasonably well and able to carry out daily activities, as measured by a standard scale (ECOG performance score of 0, 1, or 2).
  • People whose blood counts, liver function, and kidney function meet the required levels as tested by blood tests (confirm specific values with the trial site).
  • Women who could become pregnant must have a negative pregnancy test within 72 hours before joining the trial, and both men and women who could have children must agree to use effective contraception during the trial and for at least 6 months after treatment ends.
  • People aged 18 years or older.
  • People who are willing and able to sign consent forms, provide tissue samples, attend follow-up appointments, and comply with the treatment schedule.

Who may not be able to join:

  • People whose cancer has spread to other parts of the body (metastatic disease), confirmed by imaging or cell testing.
  • People who have previously received radiation therapy for pancreatic cancer.
  • People who have previously received a combination of chemotherapy and radiation therapy that overlapped with the area that would be treated in this trial.
  • People diagnosed with adenosquamous carcinoma of the pancreas (a different subtype of pancreatic cancer).
  • People who have received chemotherapy within 2 weeks before joining the trial, or who are still experiencing significant side effects from earlier chemotherapy. People who received certain types of immunotherapy or antibody treatments within 28 days before joining, or who still have unresolved significant side effects from those treatments (confirm details with the trial site).
  • People who are currently receiving other chemotherapy or biological treatments at the same time as this trial.
  • People with a medical history of a condition called ataxia telangiectasia, or any other documented condition that causes unusual sensitivity to radiation. This also includes people with certain specific genetic mutations in the ATM gene that are considered likely harmful (confirm specific mutation details with the trial site).
  • People who currently have a serious active infection that requires intravenous (IV) antibiotics.

Important: Always verify eligibility with the trial site directly before applying.

Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 8 July 2026
This study is not part of the standard drug-approval phase pathway (for example an observational, device, behavioural, or registry study), so a phase success rate does not apply.

Contact this trial

Principal Investigator: Joshua Meyer, MD, Fox Chase Cancer Center

Phone: 215-728-2667

Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.

GP referral letter

Print a one-page summary to share with your doctor.

Trial details

Status
Recruiting
Phase
Not Applicable
Sponsor
Fox Chase Cancer Center
Registry
ClinicalTrials.gov
Start date
20 August 2025
Est. completion
1 August 2028

Where this trial is recruiting

🇺🇸 United States

Primary endpoints

The rate of acute and late grade ≥3 gastrointestinal toxicity occurring within 3 months of treatment possibly, probably or definitely related to radiation.

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

Data last synced from ClinicalTrials.gov: 8 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov