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Study identifier: NCT04903782 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Cancer Predisposition Testing by Family-based Whole-genome Sequencing (WGS) in Every Child With Newly Diagnosed Cancer

Condition: Neoplastic Syndromes, Hereditary · Cancer · Genetic Predisposition to Disease  ·  Sponsor: Sydney Children's Hospitals Network

PhaseN/A
Planned participants270
Who can joinAll sexes, N/A to 21 Years
Healthy volunteersNo

About this study

Assessment of the utility of family-based (trio) whole-genome sequencing for cancer predisposition testing in sequential newly diagnosed paediatric and adolescent cancer patients

This description comes directly from the study's public registry record.

Talk to the study team

Clinical Trials Manager  ·  +61 2 9382 3122  ·  SCHN-PREDICT@health.nsw.gov.au

Always discuss trial participation with your own doctor first.

Locations (3)

John Hunter Children's HospitalNewcastle, New South Wales, AustraliaRecruiting
Sydney Children's HospitalSydney, New South Wales, AustraliaRecruiting
The Children's Hospital at WestmeadSydney, New South Wales, AustraliaRecruiting

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Source record: clinicaltrials.gov/study/NCT04903782