Phase 2 Pancreatic Cancer Trial, Recruiting NCT07627711 Sponsor: Beijing Biotech Condition: Pancreatic Cancer
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Phase 2 Pancreatic Cancer Trial, Recruiting

NCT07627711
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 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 and has either spread or is locally advanced, and has continued to grow after at least one previous standard cancer treatment, or for whom standard treatment was not suitable or not tolerated.
  • People who have at least one tumour that can be measured using standard imaging criteria.
  • People whose tumour tissue tests positive for certain proteins — either mesothelin and/or MUC1 (for one treatment arm), or claudin 18.2 and/or MUC1 (for another treatment arm) — based on laboratory testing of a tissue sample (confirm with trial site for specific thresholds).
  • People who are in reasonably good general health, able to carry out light activity and care for themselves, as assessed by a standard health scale (ECOG score of 0 or 1).
  • People whose blood counts, liver function, and kidney function meet the minimum levels required by the trial.
  • People with a life expectancy of at least 12 weeks.
  • People who are not pregnant, as confirmed by a test, and who agree to use effective contraception during the trial and for a set period afterwards.
  • People who are able to understand the study and are willing to sign a written consent form.

Who may not be able to join:

  • People with active or untreated cancer that has spread to the brain or the lining of the brain or spinal cord.
  • People with a serious, uncontrolled infection at the time of enrolment.
  • People with active hepatitis B or hepatitis C with detectable levels of the virus in their blood, or an uncontrolled HIV infection.
  • People who have previously had a bone marrow transplant using donor cells, or a transplanted solid organ.
  • People who have received a gene-modified cell therapy (such as CAR-T or CAR-NK therapy) within the past 6 months, or who have previously received treatment targeting the same proteins this trial targets.
  • People who require ongoing use of immune-suppressing medicines, such as long-term steroid use above a basic maintenance dose.
  • People with serious heart conditions, such as a recent heart attack, an uncontrolled irregular heartbeat, or severe heart failure, within a timeframe defined by the trial.
  • People with an active autoimmune disease that has required systemic treatment within the past 2 years (hormone or vitamin replacement therapy is generally allowed — confirm with trial site).
  • People who are pregnant or breastfeeding.
  • People with a medical, psychiatric, or personal situation that, in the treating doctor's judgement, could affect safe participation in the trial or the reliability of results.

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 26 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 March 2026
Est. completion
14 April 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: 26 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