Clinical Trial

Study of High-Precision Evaluation of Molecular ResiduaL Disease Through a PlatfOrm for Cancer TracKing and Interception (SHERLOCK)

Study acronym: SHERLOCK
Recruiting
View on ClinicalTrials.gov →
Summary
This study will collect, annotate, and sequence biospecimens (blood, tissue, urine, saliva and surgery drainage) from patients across different cancer types to detect molecular residual disease (MRD). Imaging scans and clinical data will also be gathered. This will allow for early cancer interception, and hopefully prolong relapse-free survival across tumor types. Results of ctDNA testing will be provided for clinical decisions and to determine eligibility for other linked interventional interception therapeutic studies, each of which will have a separate protocol.
Protocol Amendment History 1 amendment
This ClinicalTrials.gov record has been amended once since 2026-04-09.
Trial Details
NCT Number NCT07524114
Lead Sponsor University Health Network, Toronto
Collaborators: Princess Margaret Hospital, Canada
Conditions Breast Cancer, Lung Cancer, Melanoma, Gynecologic Cancer, Genitourinary Cancer, Pancreatobiliary Cancer, Gastrointestinal Cancer, Head and Neck Cancer +2 more
Enrollment 7,000 participants
Start Date 2026-03-31
Primary Completion 2031-03-31 (estimated)
Study Completion 2031-03-31 (estimated)
Updated on ClinicalTrials.gov 2026-05-11