Phase 2 Pancreatic Cancer Trial, Recruiting NCT07644559 Sponsor: Verastem, Inc. Condition: Pancreatic Cancer
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Phase 2 Pancreatic Cancer Trial, Recruiting

NCT07644559
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 have been diagnosed with pancreatic ductal adenocarcinoma (a specific type of pancreatic cancer), confirmed by laboratory testing of tissue samples
  • People who have at least one area of cancer that can be measured on a scan, according to a standard set of measurement rules
  • People whose cancer has tested positive for a specific genetic change called a KRAS G12D mutation (a tissue sample is needed for further confirmation testing by the trial laboratory)
  • People who are generally well enough to carry out normal daily activities, with little or no limitation (as rated by a standard medical scale)
  • People whose liver, kidneys, and other organs are functioning adequately
  • For the second-line treatment group: People who have received only one prior treatment for their cancer that has spread to other parts of the body — or whose cancer came back within 6 months of completing an earlier course of treatment after surgery
  • For the first-line treatment group: People who have not yet received treatment for cancer that has spread, or who have received no more than one cycle of standard treatment for it

Who may not be able to join:

  • People whose cancer has other related genetic mutations (in the same family of mutations as KRAS) in addition to the KRAS G12D mutation
  • People who have received any other cancer treatment within 4 weeks before the first trial treatment dose (or within a shorter drug-specific timeframe, whichever comes first)
  • People who have had major surgery within 4 weeks before the first trial treatment dose
  • People who have had radiation therapy within 1 week before the first trial treatment dose, or radiation to the brain or lungs within 2 weeks before the first trial treatment dose
  • People with a history of serious lung inflammation caused by a medication
  • People who have previously been treated with a drug that directly targets the RAS protein
  • People who have cancer that has spread to the brain and is either untreated or currently causing symptoms
  • People who have taken certain medications that strongly affect how the body processes drugs (specific enzyme inhibitors or inducers), or certain other medications with a very narrow safe dosage range, within 14 days before the first trial treatment dose (or within a shorter drug-specific timeframe, whichever comes first)
  • People who have taken proton pump inhibitors (such as medications commonly used for heartburn or stomach acid) or a similar type of stomach acid medication within 5 days before the first trial treatment dose
  • People who are unable to swallow tablets or capsules
  • Additional criteria not listed here may also apply (confirm with trial site)

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 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: 7812924204

Australian sites

ICON Kurralta Park, Kurralta Park, South Australia
08 84740420
ICON Cancer Centre, South Brisbane,

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
Verastem, Inc.
Registry
ClinicalTrials.gov
Start date
16 June 2026
Est. completion
1 June 2027

Where this trial is recruiting

🇦🇺 Australia 🇺🇸 United States

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

Primary endpoints

Confirmed ORR by blinded independent central review (BICR) per RESIST v1.1; To characterize the safety and tolerability of VS-7375 monotherapy or in combination with cetuximab, administered on a daily oral schedule in participants with KRAS G12D-mutated PDAC.

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