Phase 2 Pancreatic Cancer Trial, Recruiting NCT07480928 Sponsor: Beijing Biotech Condition: Pancreatic Cancer
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Phase 2 Pancreatic Cancer Trial, Recruiting

NCT07480928
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 aged 18 to 75 years old at the time of giving consent to participate.
  • People who have been diagnosed with pancreatic ductal adenocarcinoma (a specific type of pancreatic cancer) confirmed through laboratory testing of tissue or cell samples.
  • People whose cancer cannot be surgically removed, has spread, and has continued to grow after at least one previous standard cancer treatment — or where standard treatment was not tolerated or was not an option.
  • People who have at least one tumour that can be measured using standard imaging criteria.
  • People whose tumour tissue tests positive for certain proteins: Arm A requires the tumour to show mesothelin (MSLN) and/or MUC1; Arm B requires the tumour to show Claudin 18.2 (CLDN18.2) and/or MUC1 — tested on stored or freshly taken biopsy samples (confirm with trial site for exact thresholds).
  • People with a good general level of physical functioning, rated 0 or 1 on a standard scale used by doctors (meaning fully active or able to carry out light activity).
  • People whose blood counts and organ function (including liver and kidneys) meet minimum health thresholds set by the trial (confirm with trial site for exact values).
  • People with a life expectancy of at least 12 weeks.
  • People who are not pregnant (a negative pregnancy test is required for those who could become pregnant), and those who agree to use effective contraception throughout the study and for a set period afterwards.
  • People who are able to understand the study information and are willing to sign a consent form.

Who may not be able to join:

  • People who have active or untreated cancer that has spread to the brain or the lining around the brain and spinal cord.
  • People with a serious, uncontrolled infection (bacterial, fungal, or viral).
  • People with active hepatitis B or hepatitis C where the virus is still detectable in the blood, or people with uncontrolled HIV infection.
  • People who have previously had a bone marrow or stem cell transplant from a donor, or a solid organ transplant (such as a kidney or liver).
  • People who received a gene-modified cell therapy (such as CAR-T or CAR-NK treatment) within the past 6 months, or who have previously had treatment targeting the same proteins this trial focuses on.

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 13076790030

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
Sponsor
Beijing Biotech
Registry
ClinicalTrials.gov
Start date
2 February 2026
Est. completion
14 February 2027

Where this trial is recruiting

🇨🇳 China

Primary endpoints

Incidence of dose-limiting toxicities (DLTs); Incidence and severity of treatment-emergent adverse events (TEAEs); Maximum tolerated dose (MTD)

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