Early Phase 1 Pancreatic Cancer Trial, Recruiting NCT05098197 Sponsor: Shanghai Juncell Therapeutics Condition: Pancreatic Cancer
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Early Phase 1 Pancreatic Cancer Trial, Recruiting

NCT05098197
Recruiting Early 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:

  • Adults between 18 and 75 years of age
  • People who have been diagnosed with primary, relapsed, or spread (metastatic) cancer of the liver, bile ducts, or pancreas, confirmed by a tissue sample
  • People whose doctors estimate they have a life expectancy of more than 3 months
  • People who are reasonably functional in daily life (based on standard performance scoring scales used by doctors)
  • People whose standard treatment options have stopped working, or for whom no standard treatment options exist
  • People who have a tumour area that doctors can safely sample (biopsy or remove), or who have a body fluid (such as fluid build-up in the abdomen) from which immune cells can be collected
  • People who have at least one tumour that can be measured and monitored during the trial
  • People whose blood test results (taken within 7 days before joining) meet specific thresholds for white blood cells, infection-fighting cells, immune cells, platelets, haemoglobin, clotting measures, kidney function, liver enzyme levels, and bilirubin levels (confirm specific values with trial site)
  • People who have no medical reason preventing them from undergoing a biopsy or minor surgical procedure
  • People of childbearing potential who are willing to use highly effective contraception from the time of signing consent and for one year after completing a specific part of the treatment
  • People who have stopped any cancer-targeting treatments — including radiotherapy, chemotherapy, or biological therapies — at least 28 days before immune cells are collected
  • People who are able to understand and sign the consent form
  • People who are able to attend follow-up visits and meet the other requirements of the trial

Who may not be able to join:

  • People who need daily steroid medication (such as prednisone) at doses above 15mg per day, or who have autoimmune conditions requiring immune-modifying treatment
  • People with significantly reduced lung function based on specific breathing test measurements (confirm details with trial site)
  • People with serious heart conditions, such as severe heart failure, significantly low blood pressure, uncontrolled coronary artery disease, very low heart pumping function, or serious heart rhythm or conduction problems
  • People who have HIV infection or a positive HIV antibody test, active hepatitis B or C infection, syphilis, or a positive syphilis antibody test
  • People with serious physical or mental health conditions
  • People who have an active whole-body infection requiring treatment, or who have positive blood cultures or imaging showing signs of infection
  • People who have received other treatments — including other medicines, biological therapies, chemotherapy, or radiotherapy — within the past month, or who are currently receiving such treatments
  • People with a history of allergic reactions to substances similar to those used in cell-based therapies
  • People who have previously received immunotherapy and experienced severe immune-related side effects (rated above Level 3)
  • People who still have ongoing side effects from previous cancer treatments that have not returned to a mild or resolved level (with some exceptions, such as hair loss, at the investigator's discretion)
  • People who are pregnant or breastfeeding
  • People who have previously had an organ transplant, a bone marrow or stem cell transplant from a donor, or kidney replacement therapy (such as dialysis)
  • People who the trial doctors consider to have other serious health conditions or other reasons that make participation unsuitable

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 21 July 2026
Early Phase 1 studies are small, early exploratory studies that come before the main Phase 1 to 3 testing, so a standard phase success rate does not apply.

Contact this trial

Phone: 086-18001759113

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
Early Phase 1
Sponsor
Shanghai Juncell Therapeutics
Registry
ClinicalTrials.gov
Start date
26 September 2021
Est. completion
25 September 2026

Where this trial is recruiting

🇨🇳 China

Primary endpoints

Adverse Events (AE); Objective Response Rate (ORR); Disease Control Rate (DCR); Duration of Response (DOR); Progression-Free Survival (PFS); Overall Survival (OS)

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: 21 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