Phase 1 Pancreatic Cancer Trial, Recruiting NCT06816823 Sponsor: Changhai Hospital Condition: Pancreatic Cancer
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Phase 1 Pancreatic Cancer Trial, Recruiting

NCT06816823
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 aged between 18 and 70 years old
  • People who have locally advanced, spread, or returned pancreatic cancer, where a specific protein called eGR1 is found at certain levels on their tumour cells (confirmed through lab testing of tumour tissue), and whose cancer has not responded to standard treatment, who could not tolerate standard treatment, or who have chosen not to have standard treatment
  • People who have at least one tumour that can be measured on a scan, according to standard measurement guidelines
  • People who have not received any cancer treatment for at least 4 weeks before joining
  • People whose general health and ability to carry out daily activities falls within an acceptable range on a standard medical scale (confirm with trial site)
  • People whose life expectancy is estimated to be more than 12 weeks
  • People whose blood cell counts and kidney function are within the required ranges, as confirmed by blood tests (confirm with trial site for specific numbers)
  • People whose liver function and other blood chemistry results are within the required ranges, as confirmed by blood tests (confirm with trial site for specific numbers)
  • People who are willing to take part and agree to sign a consent form

Who may not be able to join:

  • People whose cancer has spread to the brain or central nervous system
  • People who have previously received a type of treatment where immune cells are collected, modified, and put back into the body
  • People who have any active, uncontrolled infection, including hepatitis B, hepatitis C, HIV, or syphilis
  • People who have received a live vaccine within the past 3 months
  • People with a history of a weakened immune system
  • People with an active autoimmune disease (where the immune system attacks the body's own tissues)
  • People with serious health conditions, including severe breathing problems, serious heart conditions (such as a recent heart attack, unstable chest pain, certain heart rhythm problems, or poor heart pump function), poorly controlled diabetes or other metabolic conditions, or serious gut problems such as significant bleeding, severe diarrhoea, or a blockage requiring medical intervention
  • People who may have a severe allergic reaction or other known contraindication to the study drug or its ingredients
  • People who are pregnant or breastfeeding
  • People with a history of neurological or psychological disorders
  • People whom the trial doctors consider unsuitable for the study for other medical reasons

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 14 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: Zhuan Liao, MD PhD, Changhai Hospital

Phone: +86-13124828854

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
Changhai Hospital
Registry
ClinicalTrials.gov
Start date
7 April 2025
Est. completion
1 September 2025

Where this trial is recruiting

🇨🇳 China

Primary endpoints

Dose-limiting toxicity (DLT); Maximum tolerated dose (MTD); Treatment-emergent adverse event (TEAE) and treatment-emergent serious adverse event (TESAE); Number of participants with abnormal clinical laboratory parameters reported as TEAE; Number of participants with abnormal vital signs reported as TEAE; Number of participants with change from baseline in QT/QTc interval in electrocardiogram

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: 14 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