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Adding Zoldonrasib to Chemotherapy for Pancreatic Cancer Treatment

NCT07621718 · Recruiting
About this trial

This study looks at how well a new medicine called zoldonrasib works when given with chemotherapy for people with a specific type of pancreatic cancer. The goal is to see if this combination helps patients live longer and have better outcomes compared to a placebo, which is a treatment that looks like the real medicine but has no active ingredients. The trial focuses on patients with metastatic KRAS G12D-mutated pancreatic adenocarcinoma who have not had treatment before.

Locations and contact

This trial is running at 3 locations in the United States. All of them are currently recruiting.

United States3 locations · 3 recruiting
  • Johns Hopkins UniversityBaltimore, MarylandRecruiting
  • Moffitt Cancer CenterTampa, FloridaRecruiting
  • Piedmont HealthcareAtlanta, GeorgiaRecruiting
Who to ask about joining
Revolution Medicines Study Director1-844-2-REVMEDmedinfo@revmed.com
Who can join

Participants must be at least 18 years old and can be men or women. They need to have a confirmed diagnosis of pancreatic adenocarcinoma and a specific KRAS mutation. People who have had other cancer treatments before are not eligible to join. The trial team will confirm who can participate.

What happens during the trial

Participants will be randomly placed into one of two groups. One group will receive zoldonrasib along with a type of chemotherapy chosen by the doctor. The other group will receive a placebo with the same type of chemotherapy. All treatments are given as oral tablets or through IV infusions.

The trial team

The trial is sponsored by Revolution Medicines, Inc., which is responsible for the study.

Important dates

The trial started on May 22, 2026, and is expected to finish by April 22, 2030. It is currently recruiting new participants.

Additional information

The trial's ID number is NCT07621718. This is a Phase 3 trial, which means it is looking at how well the treatment works and how safe it is. It is regulated by the FDA and hopes to include about 670 participants.

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