Phase 1 Pancreatic Cancer Trial, Recruiting NCT06158139 Sponsor: UNC Lineberger Comprehensive Cancer Center Condition: Pancreatic Cancer
Back to Pancreatic Cancer

Phase 1 Pancreatic Cancer Trial, Recruiting

NCT06158139
Recruiting Phase 1

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 are willing and able to give written consent to take part and to allow their personal health information to be shared as part of the study.
  • People who are 18 years of age or older at the time of giving consent.
  • People who have a relatively good level of physical functioning, rated 0 or 1 on a standard scale used in cancer research (confirm with trial site for details on what this means in practice).
  • People who have been diagnosed with a specific type of pancreatic cancer called pancreatic ductal adenocarcinoma, confirmed through a tissue or cell sample.
  • Women who could become pregnant must be willing to either avoid heterosexual activity or use two reliable forms of contraception from the time of consent until 6 months after finishing the study treatment.
  • Men with female partners must either have had a vasectomy or agree to use a double barrier method of contraception (such as a condom plus spermicidal agent) from the first dose of treatment through 3 months after the cell infusion therapy.

Who may not be able to join:

  • People who have or have had another type of cancer whose history or treatment could affect how safely or accurately the study results can be assessed.
  • People who, in the judgment of the study doctor, are not willing or able to follow the study procedures as required.

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 28 July 2026
Phase 1: approximately ~10% 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: Ashwin Somasundaram, MD, UNC Lineberger Comprehensive Cancer Center

Phone: +1 919-445-4208

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 1
Sponsor
UNC Lineberger Comprehensive Cancer Center
Registry
ClinicalTrials.gov
Start date
18 July 2024
Est. completion
1 April 2028

Where this trial is recruiting

🇺🇸 United States

Primary endpoints

Number of participants with adverse event; Cytokine Release Syndrome; Neurotoxicity

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: 28 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