Phase 1 Pancreatic Cancer Trial, Recruiting NCT04157127 Sponsor: Diakonos Oncology Corporation Condition: Pancreatic Cancer
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Phase 1 Pancreatic Cancer Trial, Recruiting

NCT04157127
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 18 years of age or older, of any gender
  • People who have been diagnosed with a specific type of pancreatic cancer (adenocarcinoma or adenosquamous carcinoma) that doctors consider possibly removable by surgery, either upfront or after initial chemotherapy and/or radiation treatment
  • People whose kidneys, liver, bone marrow, and immune system are functioning at adequate levels based on blood tests taken within 28 days before joining the trial
  • People whose general health and ability to carry out daily activities meet a minimum standard (confirm with trial site)
  • Women who could become pregnant must agree to use highly effective contraception starting at least 30 days before the first vaccination and continuing for at least 12 weeks after the last vaccination
  • Women who could become pregnant must have a negative blood pregnancy test before vaccination
  • Men who could father children must agree to use condoms or other effective contraception during the trial and for 12 weeks after the last vaccination
  • People who agree not to donate blood for up to 90 days after their last vaccination
  • People who are willing and able to follow the trial requirements and sign a consent form

Who may not be able to join:

  • People whose pancreatic cancer cannot be surgically removed or has spread to other parts of the body (stage IV)
  • People with HIV who also have a detectable viral load
  • People with active hepatitis B or hepatitis C infections (though certain people with past hepatitis B or C exposure without active infection may still be eligible — confirm with trial site)
  • People with any active autoimmune disease, immune deficiency, or a history of a nerve condition called Guillain-Barré syndrome; people with certain skin conditions such as eczema, psoriasis, or vitiligo may still be eligible if their condition is mild, well-controlled, affects less than 10% of the body, and has not required strong treatments in the past 12 months (confirm with trial site)
  • People receiving a chemotherapy regimen before surgery that does not meet standard treatment guidelines, as determined by the trial doctor
  • Women who are pregnant, breastfeeding, or who could become pregnant but decline to follow the contraception requirements outlined in the trial; women must have been without a menstrual period for at least 12 months to be considered past childbearing age
  • People who are unwilling or unable to follow the trial procedures or provide consent
  • People with severe or uncontrolled medical conditions that the trial doctor believes would affect safe participation, including but not limited to thyroid problems, active autoimmune disorders, untreated viral hepatitis, or autoimmune hepatitis
  • People who require ongoing treatment with steroid medications at a moderate-to-high dose (10 mg per day of prednisone or equivalent or more) or any other ongoing medication that suppresses the immune system

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 22 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: Benjamin Musher, MD, Baylor College of Medicine

Phone: 713-798-4292

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
Diakonos Oncology Corporation
Registry
ClinicalTrials.gov
Start date
3 August 2020
Est. completion
1 June 2026

Where this trial is recruiting

🇺🇸 United States

Primary endpoints

Safety of DC Therapy; Number of participants who experienced Dose Limiting Toxicities (DLTs)

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: 22 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