Phase 1 Pancreatic Cancer Trial, Recruiting NCT06179160 Sponsor: Incyte Corporation Condition: Pancreatic Cancer
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Phase 1 Pancreatic Cancer Trial, Recruiting

NCT06179160
Recruiting Phase 1 🇦🇺 Australian site

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 18 years of age or older.
  • People who have a locally advanced or spreading solid tumour cancer that has a specific genetic change called a KRAS G12D mutation.
  • For certain parts of the trial: People whose cancer has continued to grow despite previous standard treatments, who could not tolerate standard treatments, who are not suitable for standard treatments, who have chosen not to pursue available treatments, or for whom no standard treatment exists to improve their outcome.
  • People who meet additional requirements specific to the particular group or stage of the trial, as defined in the trial protocol (confirm with trial site).
  • People whose general health and ability to carry out daily activities falls within a certain range, measured by a standard medical scale called the ECOG score of 0 or 1 — meaning fully active or restricted in strenuous activity but able to carry out light work (confirm with trial site).

Who may not be able to join:

  • People who have previously received any treatment that targets the KRAS G12D mutation.
  • People who have been diagnosed with another invasive cancer within the past year before starting the trial.
  • People who have a history of having received an organ transplant, including bone marrow or stem cell transplants.
  • People who have a serious medical condition that is not well controlled.
  • People who have a history of, or currently have, an abnormal heart rhythm reading on an ECG (a test that measures the heart's electrical activity).
  • People whose organs such as the liver, kidneys, or bone marrow are not functioning at an adequate level.

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 1: approximately ~10% 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: Incyte Medical Monitor, Incyte Corporation

Phone: 1.855.463.3463

Australian sites

Chris Obrien Lifehouse, Camperdown, New South Wales
St Vincent'S Hospital Sydney, Darlinghurst, New South Wales
Peter Maccallum Cancer Centre, Melbourne, Victoria
The Alfred Hospital, Melbourne, Victoria
Linear Clinical Research, Nedlands, Western Australia

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 1
Sponsor
Incyte Corporation
Registry
ClinicalTrials.gov
Start date
4 January 2024
Est. completion
1 January 2027

Where this trial is recruiting

🇦🇺 Australia 🇧🇪 Belgium 🇨🇦 Canada 🇫🇷 France 🇮🇹 Italy 🇯🇵 Japan 🇪🇸 Spain 🇺🇸 United States

5 site(s) in Australia. Confirm current status and contact details directly with the trial site.

Primary endpoints

Number of participants with Dose Limiting Toxicities (DLTs); Number of participants with Treatment-emergent Adverse Events (TEAEs); Number of participants with TEAEs leading to dose modification or discontinuation

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