Plain-English translation of NCT07481383 on ClinicalTrials.gov ↗ · Source last updated · Translation generated · How we translate trials
Phase 1 — Testing in a small group (usually 20–80 people) to find a safe dose and watch for side effects.
This is one of the first times this treatment has been tested in people.
This is a first-in-human study testing a new implantable device called the ACT-IOP-003 that delivers the chemotherapy drug gemcitabine directly to pancreatic cancer tumors. Instead of receiving chemotherapy through an IV in your arm (where it circulates throughout your body), this device is surgically placed on or near the tumor to deliver the medication locally. The trial is designed to see if this approach is safe, well-tolerated, and whether it works better than traditional IV chemotherapy.
Standard chemotherapy for advanced pancreatic cancer can cause significant side effects because the medication travels throughout the entire body. By delivering this medication directly to the tumor site using an implanted device, researchers hope to reduce side effects while potentially improving how well the treatment works against the cancer.
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You will have a surgical procedure to implant the device directly on your pancreas. After surgery, you will receive treatment through the device once or twice per week for 8 weeks, depending on which study group you're assigned to. Over the course of 24 weeks total, you will visit the clinic for regular blood and urine tests, provide stool samples to monitor safety, and have at least three imaging scans (CT scans) to check how your tumor is responding.
AI-generated summary from trial data · Jul 17, 2026 · Not medical advice
United States