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Rare and childhood cancer multi-omics for precision medicine

Rare and childhood cancer multi-omics for precision medicine

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
TCTR
Registry ID
TCTR20211015001
Enrollment
1000
Registered
2021-10-15
Start date
2022-01-05
Completion date
Unknown
Last updated
2026-08-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

High-risk neuroblastoma, refractory or relapsed Osteosarcoma Non-rhabdosarcoma solid tumors Brain tumors: embryonal tumors &amp

Interventions

patients who are under 18 years of age with diagnosed high-risk, refractory, or relapsed diseases of pediatric neuroblastoma, osteosarcoma, brain tumors (including embryonal germline tumors and glioma
Diagnostic
rare pediatric cancer

Sponsors

Health System Research Institute
Lead Sponsor

Eligibility

Sex/Gender
All
Age
No minimum to 18 Years

Inclusion criteria

Inclusion criteria: Age less than 18 years with High-risk neuroblastoma, refractory or relapsed or Osteosarcoma or Non-rhabdosarcoma solid tumors or Brain tumors: embryonal tumors & diffused/high grade gliomas or Atypical teratoid/rhabdoid tumor

Exclusion criteria

Exclusion criteria: 1. No biological parents available 2. Refusal to participate in the study

Design outcomes

Primary

MeasureTime frame
Cancer predisposing gene 1 month Not statistical method

Secondary

MeasureTime frame
Novel targeted therapy 6 months Not statistical method

Countries

Thailand

Contacts

Public ContactUsanarat Anurathapan

Department of Pediatrics, Faculty of Medicine Ramathibodi Hospital, Mahidol University

usanarat.anu@mahidol.ac.th0642345626

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 9, 2026