Phase 2 Pancreatic Cancer Trial, Recruiting NCT06453486 Sponsor: University Health Network, Toronto Condition: Pancreatic Cancer
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Phase 2 Pancreatic Cancer Trial, Recruiting

NCT06453486
Recruiting Phase 2

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 locally advanced pancreatic cancer (cancer confirmed by tissue or cell testing).
  • People whose pancreatic tumour measures less than 8.0 cm at its widest point at the time of treatment planning (final confirmation depends on meeting certain radiation safety limits for surrounding organs).
  • People who are in generally good physical condition, able to carry out normal daily activities with little or no limitation (confirm with trial site for exact fitness level required).
  • People whose doctor estimates they are expected to live for more than 6 months.
  • People who have already received first-line chemotherapy for this cancer for at least 16 weeks without the cancer getting worse, and who have waited at least 2 weeks after finishing that chemotherapy before joining the trial.
  • People who are able to understand the study information and are willing to sign a consent form.
  • Women who are not pregnant or breastfeeding, and women who could potentially become pregnant must have a negative pregnancy test within 4 weeks before joining; women who are breastfeeding must stop before joining.

Who may not be able to join:

  • People whose cancer has spread to other parts of the body (metastatic disease).
  • People under 18 years of age.
  • People who have previously received chemotherapy or any other anti-cancer treatment for cancer that had already spread to other parts of the body.
  • People who have previously had radiation therapy to the upper abdomen area in a way that would overlap with the radiation planned for this trial.
  • People who are currently receiving any anti-cancer treatment, including chemotherapy.
  • People with serious uncontrolled health conditions such as active infection, severe heart failure, unstable chest pain, irregular heart rhythm, or mental health or social circumstances that would make it difficult to follow the study requirements.
  • Women who are pregnant or breastfeeding.
  • People with any other condition that, in the treating doctor's judgment, would make participation unsafe or difficult.
  • People with a history of another type of cancer, unless they have been free of that cancer for at least 2 years and are considered low risk for it returning. An exception applies to people diagnosed and treated within the past 5 years for certain skin cancers (basal cell or squamous cell carcinoma) or early-stage cervical cancer (in situ), who may still be considered eligible.
  • People with certain conditions that make high-dose targeted radiation unsafe, such as scleroderma (a connective tissue disease) or stomach or bowel ulcers or perforations in the area to be treated.
  • People with conditions that are not compatible with MRI scanning, such as having a heart pacemaker, certain metal objects in the body, or severe claustrophobia. People who have previously had a severe allergic reaction to the MRI contrast agent gadolinium, or who have severe kidney disease (confirm with trial site for exact kidney function threshold), would also not be able to participate in the MRI component of this trial.

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 13 July 2026
Phase 2: approximately ~30% of drugs entering this phase reach regulatory approval, based on published industry-wide historical data. This is not specific to this trial.
Phase success rates shown are historical industry-wide averages based on published data. They are not a prediction for this specific trial or your individual situation.

Contact this trial

Principal Investigator: Erica Tsang, MD, University Health Network, Toronto

Phone: 647-539-6498

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
Phase 2
Registry
ClinicalTrials.gov
Start date
12 March 2025
Est. completion
1 April 2030

Where this trial is recruiting

🇨🇦 Canada

Primary endpoints

Overall survival (OS)

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: 13 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