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NCT07524114: SHERLOCK

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

Recruiting now Last updated 13 April 2026
What this trial tests

trial in Breast Cancer in 7,000 participants. Currently enrolling.

Timeline
31 March 2026
Primary endpoint
31 March 2031
31 March 2031

Quick facts

Lead sponsorUniversity Health Network, Toronto
StatusRecruiting now
Study typeOBSERVATIONAL
Enrollment7,000
Start date31 March 2026
Primary completion31 March 2031
Estimated completion31 March 2031
Sites1 location across Canada

Conditions studied

Sponsor

University Health Network, Toronto

Who can join

18 and older, any sex, with Breast Cancer or Lung Cancer. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

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.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Breast Cancer

Currently open trials in the same condition.

Other University Health Network, Toronto trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT07524114.