Phase 2 Pancreatic Cancer Trial, Recruiting NCT06914128 Sponsor: Bayer Condition: Pancreatic Cancer
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Phase 2 Pancreatic Cancer Trial, Recruiting

NCT06914128
Recruiting Phase 2 🇦🇺 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 (or the legal age of consent in the country where the study takes place) at the time of signing the consent form.
  • People who have at least one tumour that can be measured using standard imaging criteria (known as RECIST 1.1).
  • People whose tumour has tested positive for a specific genetic change called homozygous MTAP-deletion, confirmed through a certified laboratory test.
  • People who are relatively well and able to carry out daily activities, as measured by a standard health scale called ECOG — specifically, those rated 0 (fully active) or 1 (restricted in strenuous activity but able to do light work).

Who may not be able to join:

  • People who have had a different type of cancer in the past 2 years, with some exceptions — such as certain minor skin cancers, early-stage cervical changes, superficial bladder tumours, localised prostate cancer, or other cancers that the treating doctor considers cured or not immediately life-threatening.
  • People whose heart's electrical activity shows a prolonged interval (called QTc greater than 450 ms) on a heart tracing test — though people with a permanent pacemaker may still be considered, based on the treating doctor's assessment.
  • People with a history of significant heart failure (Class II or higher on a standard medical scale), a heart attack within the past 6 months, or serious heart rhythm problems requiring treatment — with the exception of well-controlled atrial fibrillation managed only with digoxin or beta blockers.
  • People who have had unstable chest pain (unstable angina) within the 4 weeks before starting the study treatment.

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

Phone: (+)1-888-84 22937

Australian sites

Chris O'Brien Lifehouse, Camperdown, New South Wales
Concord Repatriation General Hospital (CRGH) (Concord Hospital) - Concord Cancer Centre, Concord, New South Wales
Northern Hospital, Epping, New South Wales
Calvary Mater Hospital Newcastle - Oncology, Waratah, New South Wales

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
Registry
ClinicalTrials.gov
Start date
21 March 2025
Est. completion
17 June 2029

Where this trial is recruiting

🇦🇺 Australia 🇧🇪 Belgium 🇨🇳 China 🇨🇿 Czechia 🇩🇰 Denmark 🇮🇹 Italy 🇯🇵 Japan 🇳🇱 Netherlands 🇸🇬 Singapore 🇪🇸 Spain 🇸🇪 Sweden 🇬🇧 United Kingdom 🇺🇸 United States

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

Primary endpoints

Dose Escalation (Master and Intervention Cohort 1): Number of participants with treatment-emergent adverse events (TEAEs); Dose Escalation (Master and Intervention Cohort 1): Number of participants with treatment-emergent serious adverse events (TESAEs); Dose Escalation (Master and Intervention Cohort 1): Severity of treatment-emergent adverse events (TEAEs) and treatment-emergent serious adverse events (TESAEs); Dose Escalation (Master and Intervention Cohort 1): Incidence of dose-limiting toxicities (DLTs); Dose Escalation (Master and Intervention Cohort 1): Number of participants with DLTs;...

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