Phase 2 Pancreatic Cancer Trial, Recruiting NCT06423326 Sponsor: Emory University Condition: Pancreatic Cancer
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Phase 2 Pancreatic Cancer Trial, Recruiting

NCT06423326
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 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.

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 27 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: 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

Status
Recruiting
Phase
Phase 2
Registry
ClinicalTrials.gov
Start date
6 August 2024
Est. completion
31 December 2026

Where this trial is recruiting

🇺🇸 United States

Primary endpoints

Clinical Response Rate to Neoadjuvant Chemotherapy

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: 27 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