Phase 2 Pancreatic Cancer Trial, Recruiting NCT06782932 Sponsor: Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins Condition: Pancreatic Cancer
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Phase 2 Pancreatic Cancer Trial, Recruiting

NCT06782932
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 newly diagnosed with pancreatic cancer (a specific type called adenocarcinoma), confirmed by a biopsy.
  • The cancer must be considered removable by surgery, as assessed by the study team.
  • People who agree to have a tumor biopsy as part of the study.
  • People who are generally well enough to carry out daily activities with little to no limitation (as measured by a standard health performance scale called ECOG, scored 0 or 1).
  • People whose heart, liver, kidneys, and other organs are functioning well enough, based on blood and other lab tests specified by the study.
  • Women who could become pregnant must have a negative blood pregnancy test before joining.
  • Both men and women must agree to use an approved form of contraception for the duration of the study.

Who may not be able to join:

  • People who have already received any treatment specifically targeting pancreatic cancer, or any prior cancer immunotherapy (treatments for symptoms only may be allowed — confirm with trial site).
  • People who have been diagnosed with another cancer that could affect the safety or results of this study.
  • People with serious uncontrolled health conditions, such as an uncontrolled infection, heart failure, unstable chest pain, irregular heartbeat, cancer that has spread to other parts of the body, or mental health or personal circumstances that would make it hard to follow the study requirements.
  • People with an active autoimmune disease (a condition where the immune system attacks the body's own tissues).
  • People who have taken high-dose steroid medications or immune-suppressing drugs within 14 days before the first study treatment (confirm with trial site for exact dose thresholds).
  • People with an active infection that requires treatment with medications that work throughout the whole body.
  • People with a known history of HIV.
  • People with active or ongoing hepatitis B or hepatitis C infection.
  • People with known active tuberculosis.
  • People with a history of certain lung conditions, including scarring of the lung tissue, acute lung disease, chronic obstructive pulmonary disease (COPD), or asthma requiring medication.
  • People who have previously had a stem cell transplant or an organ transplant from another person.
  • People who have had a major surgery requiring general anaesthesia within 28 days before the first study treatment.
  • People who have received a live vaccine within 28 days before the first study treatment.
  • People with a history of a severe allergic reaction to any monoclonal antibody medication (a type of targeted therapy).
  • People who are currently participating in another clinical trial involving a treatment.
  • People who are pregnant or breastfeeding.

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 15 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: Eric Christenson, MD, SKCCC • Johns Hopkins Medical Institution

Phone: 410-614-3644

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
27 May 2025
Est. completion
1 December 2028

Where this trial is recruiting

🇺🇸 United States

Primary endpoints

Dose Limiting Toxicities in Phase I participants; Number of participants experiencing Grade 3 or Higher study drug-related toxicities; Number of participants who form Intratumoral tertiary lymphoid structures (TLS)

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: 15 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