Plain-English translation of NCT05786716 on ClinicalTrials.gov ↗ · Source last updated · Translation generated · How we translate trials
Phase 3 — Testing in thousands of people, comparing the treatment against what doctors currently use. This is the last big step before approval.
This trial is testing whether two medications called and work together to treat rare cancers and uncommon types of common cancers that have a specific genetic change. The genetic change—called HER2 amplification or an activating HER2 mutation—is found in your tumor cells. Researchers want to see if this medication combination can help people whose cancers have this genetic marker.
Many people with rare cancers or cancers with rare genetic changes don't have good treatment options. This trial exists to find out whether this medication, already used for some cancers, might work for other cancers with the same genetic change—and eventually bring it to the NHS as a new treatment choice.
You likely qualify if…
You likely don't qualify if…
You'll start by having a biopsy and blood tests to confirm your cancer has the genetic change. Then you'll receive the two medications regularly until your cancer stops responding, you experience unacceptable side effects, or you decide to stop. You'll have blood drawn at regular intervals during treatment and at the end. After treatment ends, you'll have check-in visits every three months for two years to see how you're doing.
AI-generated summary from trial data · Jul 18, 2026 · Not medical advice
United Kingdom