Phase 2 Pancreatic Cancer Trial, Recruiting
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) through a tissue or cell sample, where the tumour is considered removable by surgery or is on the borderline of being removable — this is assessed using detailed scan results and agreed upon by a team of specialists
- People whose cancer has not spread to distant parts of the body outside the pancreas
- Adults aged 18 or older
- People who are able to give their informed consent to participate
- People who are able to attend scheduled visits and follow the study requirements
- People who are generally well enough to carry out daily activities with little or no limitation (as measured by a standard scale used in cancer care)
- People whose blood cell counts meet minimum levels: enough white blood cells (neutrophils), platelets, and red blood cells (haemoglobin), as confirmed by blood tests
- People whose liver function, kidney function, and protein (albumin) levels fall within acceptable ranges, as confirmed by blood tests
- Men, or women who are not pregnant and not breastfeeding
- Women who could become pregnant must agree to use effective contraception starting 28 days before treatment begins and throughout the treatment period
- Men must agree to use a condom during sexual contact with someone who could become pregnant, both during treatment and for 6 months after treatment ends
Who may not be able to join:
- People who have moderate or severe nerve damage (peripheral neuropathy), meaning symptoms that interfere with everyday tasks such as using a phone, cooking, or handling objects
- People with serious or uncontrolled health conditions that could affect safe participation, such as unstable chest pain (angina), a heart attack within the past 6 months, an uncontrolled irregular heartbeat, severe heart failure, uncontrolled diabetes, a serious active infection (particularly if a blocked bile duct has not been adequately treated), or significant mental health or social difficulties
- People who are pregnant or breastfeeding
- People with known disease affecting the brain or central nervous system, with some exceptions for those whose brain involvement has already been successfully treated and is stable (confirm with trial site)
- People who have had another cancer within the past 5 years or currently have another untreated cancer — though non-melanoma skin cancers and early-stage cancers confined to where they started may be exceptions (confirm with trial site)
- People with a known allergy or sensitivity to any of the medicines used in this trial
- People who are currently misusing alcohol or illicit drugs
- People who are unable or unwilling to sign the consent form
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.
Contact this trial
Principal Investigator: Hussein M Hamad, MD, MPH, Emory University Hospital/Winship Cancer Institute
Phone: 404-778-3307
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
Where this trial is recruiting
Primary endpoints
Clinical Response Rate to Neoadjuvant Chemotherapy
Can't join this trial?
Data last synced from ClinicalTrials.gov: 27 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.