Phase 3 Pancreatic Cancer Trial, Recruiting NCT06601283 Sponsor: Fudan University Condition: Pancreatic Cancer
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Phase 3 Pancreatic Cancer Trial, Recruiting

NCT06601283
Recruiting Phase 3

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 able to understand the study and are willing to sign a written consent form.
  • People aged 18 to 80 years old.
  • People with a general health and activity level rated as fairly good (rated 0–2 on a standard scale used by doctors to measure how cancer affects daily life).
  • People whose pancreatic cancer has spread to other parts of the body (metastatic) and has been confirmed by laboratory testing of tissue or cells as adenocarcinoma (a specific type of pancreatic cancer).
  • People whose blood test results show that major organs such as the liver and kidneys are working well enough.
  • People who have at least one area of cancer that can be measured on a scan, according to standard medical guidelines.
  • People whose haemoglobin (a measure of red blood cells) is at an acceptable level (8 g/dL or above).
  • People whose expected survival is at least 3 months.
  • People who are able to commit to using effective contraception throughout the study (applies to women who could become pregnant and to men).

Who may not be able to join:

  • People who have received cancer treatment for a different type of cancer within the last two years.
  • People who have previously received any cancer treatment for pancreatic cancer.
  • People whose cancer has been confirmed by laboratory testing as a type of pancreatic cancer other than adenocarcinoma.
  • People who have inflammation of the digestive tract, such as pancreatitis (inflamed pancreas), cholecystitis (inflamed gallbladder), or cholangitis (inflamed bile ducts).
  • People who are pregnant or currently breastfeeding.
  • People who have a condition called G6PD deficiency, which is an inherited condition affecting red blood cells.
  • People with serious uncontrolled health conditions that could interfere with the study, including uncontrolled infections, diabetes that cannot be managed with standard treatment, uncontrolled high blood pressure, certain heart conditions (such as severe heart failure, a heart attack in the past 6 months, unstable heart rhythm, or unstable chest pain), or a stroke within the past 3 months.
  • People with kidney disease or who are currently on dialysis.
  • People with a history of serious allergic reactions to gemcitabine, nab-paclitaxel, or similar medicines used in this study.
  • People with other serious health conditions that, in the treating doctor's judgement, could make treatment unsafe.
  • People who are unwilling or unable to follow the study procedures.

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 28 July 2026
Phase 3: approximately ~65% 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 21 64031446

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 3
Registry
ClinicalTrials.gov
Start date
22 November 2024
Est. completion
22 November 2026

Where this trial is recruiting

🇨🇳 China

Primary endpoints

Rate of anemia

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: 28 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