SHERLOCK liquid biopsy trial launched
Analysis based on 10 articles · First reported Jul 08, 2026 · Last updated Jul 08, 2026
The SHERLOCK trial represents a significant step toward personalized cancer care, potentially reducing healthcare costs by avoiding unnecessary treatments and improving patient outcomes. If successful, it could boost the liquid biopsy market and benefit companies developing related technologies.
Researchers at Princess Margaret Cancer Centre in Toronto have launched the SHERLOCK trial, a large-scale study to determine if a blood test (liquid biopsy) can detect molecular residual disease after cancer treatment. The trial, funded by a $50-million donation from the The Peter G. Peterson Foundation, aims to enroll 7,000 patients across multiple cancer types. Lead investigator Dr. Lillian Siu hopes the test can identify patients at high risk of recurrence, allowing early intervention with experimental immunotherapies, while negative results may spare patients from unnecessary treatments. The observational study will follow patients for at least five years. Although promising, liquid biopsies are not yet standard of care, and further trials are needed. The trial is a Canadian-led initiative that has already shown anecdotal success, as in the case of patient Paul Lonergan, who participated in a related study.
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