Phase 2 Pancreatic Cancer Trial, Recruiting NCT06385925 Sponsor: Tyligand Pharmaceuticals (Suzhou) Limited Condition: Pancreatic Cancer
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Phase 2 Pancreatic Cancer Trial, Recruiting

NCT06385925
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 fully understand what the study involves and have signed the consent form voluntarily.
  • People who are at least 18 years old at the time of signing the consent form (and no older than 75 for certain groups in this trial).
  • People who have a life expectancy of at least 3 months.
  • People whose general health and ability to carry out daily activities meets a specific standard (known as ECOG performance status 0 or 1 — confirm with trial site).
  • For the early phase of the trial: people whose cancer (any solid tumour that has spread or cannot be surgically removed) has been confirmed by lab testing to carry a specific genetic change called KRAS G12D, and where standard treatments have stopped working, are not tolerated, are not available, or the person is not suitable for or has chosen not to pursue standard treatment.
  • For the later phase of the trial: people with confirmed advanced or metastatic pancreatic cancer, bowel cancer, or non-small cell lung cancer that carries the KRAS G12D genetic change, with eligibility also depending on how many prior treatments have been received (confirm with trial site).
  • People whose heart, liver, and kidney function meet the required levels.

Who may not be able to join:

  • People who have cancer that has spread to the membranes surrounding the brain or spinal cord, or who have active cancer spread in the brain or central nervous system.
  • People who have received systemic cancer treatment within 21 days (or within 5 half-lives of the drug, whichever is shorter) before the first dose of the study drug.
  • People who have had intensive radiation therapy within 4 weeks, or lower-dose palliative radiation within 1 week, before the first dose of the study drug.
  • People who still have unresolved moderate or severe side effects (Grade 2 or higher) from previous cancer treatments, except for hair loss.
  • People who have taken part in another clinical trial and received an investigational drug within 21 days or 5 half-lives (whichever is shorter) before the first dose of the study drug.
  • People with a history of certain lung conditions, including interstitial lung disease, drug-related lung damage, active lung inflammation, radiation-related lung inflammation needing treatment, or other uncontrolled lung disease.
  • People who have experienced a heart attack, unstable chest pain, serious heart failure, stroke, mini-stroke, or a blood clot in the lungs within the past 6 months.
  • People who have previously received a treatment specifically targeting the KRAS G12D mutation.
  • People who have any serious medical condition, ongoing treatment, or abnormal test results that the doctor running the trial believes could affect the study results or make participation unsafe.

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 27 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

Principal Investigator: Cindy Li, Tyligand Bioscience (Shanghai) Limited

Phone: +86 021-50720081

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
Tyligand Pharmaceuticals (Suzhou) Limited
Registry
ClinicalTrials.gov
Start date
29 April 2024
Est. completion
30 October 2026

Where this trial is recruiting

🇨🇳 China 🇺🇸 United States

Primary endpoints

Dose limiting toxicities (DLTs) in phase 1 part; Objective response rate (ORR) in phase 2 part

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: 27 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