Phase 1 Pancreatic Cancer Trial, Recruiting NCT07349537 Sponsor: Revolution Medicines, Inc. Condition: Pancreatic Cancer
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Phase 1 Pancreatic Cancer Trial, Recruiting

NCT07349537
Recruiting Phase 1

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:

  • You are at least 18 years old and are willing to give your consent to take part
  • You are relatively active and able to carry out daily activities with little to no limitation (this is measured on a standard scale called ECOG — confirm with trial site if unsure where you fall)
  • You have been diagnosed with a solid tumour cancer that has spread locally or to other parts of the body, and your tumour has a specific genetic change called "KRAS G12V mutation"
  • You have already received standard treatment for your cancer type, but your cancer got worse during that treatment or you were unable to tolerate it
  • Your cancer can be measured on a scan using standard methods (called RECIST v1.1 — confirm with trial site)
  • Your bone marrow, liver, kidneys, and blood clotting are all working well enough to take part
  • You are able to swallow and take medication by mouth

Who may not be able to join:

  • Your cancer started in the brain or spinal cord
  • You have previously had treatment that specifically targeted the KRAS G12V mutation or any direct RAS-targeted therapy
  • You have any condition that might affect your ability to swallow, digest, or absorb the study drug (confirm with trial site)
  • You have had major surgery within 28 days before starting the study drug
  • You are unable or unwilling to attend the required study visits or follow the study procedures

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 9 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

Phone: 1-844-2-REVMED

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
Revolution Medicines, Inc.
Registry
ClinicalTrials.gov
Start date
8 January 2026
Est. completion
1 April 2028

Where this trial is recruiting

🇺🇸 United States

Primary endpoints

Number of patients with adverse events (AEs); Changes in vital signs; Changes in electrocardiogram (ECG) test values; Changes in clinical laboratory test values; Dose Limiting Toxicities

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: 9 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