Phase 2 Pancreatic Cancer Trial, Recruiting NCT06547736 Sponsor: Fudan University Condition: Pancreatic Cancer
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Phase 2 Pancreatic Cancer Trial, Recruiting

NCT06547736
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 chosen to take part voluntarily and have signed a consent form
  • Adults aged 18 to 75 years old, of any gender
  • People diagnosed with advanced pancreatic cancer (either spread to other parts of the body or unable to be removed by surgery), with at least one measurable area of disease visible on scans
  • People with a good general level of physical functioning — able to carry out normal daily activities with little or no limitation (rated 0 or 1 on a standard performance scale)
  • People whose life expectancy is estimated to be at least 12 weeks
  • People with adequate bone marrow and organ function based on blood tests (confirm with trial site for specific values)
  • Women of childbearing age who have had a negative pregnancy test within one week before starting the study treatment, and who are willing to use an effective form of contraception during the study and for three months after the last dose
  • Men whose partners could become pregnant, who agree to use effective contraception during the study and for six months after the last dose

Who may not be able to join:

  • People with a known allergy to the study drug or any of its ingredients
  • People who received cancer treatment in the four weeks before starting the study, or who completed palliative radiotherapy within 14 days before the first dose
  • People who have had another active cancer in the past five years
  • People who have cancer that has spread to the brain or spinal cord that has not been treated or is currently active
  • People who have not yet recovered from side effects of previous treatments to an acceptable level (confirm with trial site for specific details)
  • People with interstitial lung disease, non-infectious lung inflammation, severe uncontrolled medical conditions, active infections, or who have had a major operation within the past 28 days or have not yet recovered from one
  • People who have had a bowel blockage, or signs of one, in the six months before starting treatment — unless surgery has fully resolved the blockage
  • People who have had a serious blood clot in the heart, brain, or blood vessels in the six months before joining the study
  • People with immune system conditions present from birth or acquired (such as HIV infection), or those with active hepatitis B or hepatitis C at levels above specified thresholds (confirm with trial site for exact values)
  • People with active tuberculosis in the past year, or a history of tuberculosis from more than a year ago that was never properly treated
  • People who are currently in another clinical trial, or whose last dose in a previous clinical trial was less than four weeks ago (or within five half-lives of that study drug, whichever is shorter)
  • People considered to be at high risk of pancreatitis, including those with elevated levels of certain enzymes (amylase and/or lipase) at three times or more above the normal upper limit
  • People with uncontrolled mental health conditions, or other factors that may affect their ability to complete the study — such as alcohol, drug, or substance misuse, or legal detention
  • People who have had a major surgery (other than for diagnosis or biopsy) within 28 days before the first dose, or a minor invasive procedure (such as a biopsy, endoscopy, or drainage procedure) within seven days before the first dose
  • People whom the trial investigators consider unsuitable for other 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 21 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

Phone: +86-021-64179375

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
14 October 2024
Est. completion
1 March 2027

Where this trial is recruiting

🇨🇳 China

Primary endpoints

Recommended phase II dose (RP2D); Objective Response Rate (ORR)

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