Optimal Precision TherapIes to CustoMISE Care in Childhood and Adolescent Cancer

A companion platform trial to test novel targeted agents based on the patient's tumor profile.

Trial Details

NCT ID
NCT06208657
Phase
PHASE1 / PHASE2
Sponsor
Australian & New Zealand Children's Haematology/Oncology Group
Status
RECRUITING
Cancer Type
Brain Cancer
Interventions
  • Paxalisib
  • Opdualag
  • Irinotecan (drug)
  • Temozolomide (TMZ)
Locations (sample)
  • Newcastle, New South Wales, Australia|-32.92953,151.7801
  • Sydney, New South Wales, Australia|-33.86785,151.20732
  • Sydney, New South Wales, Australia|-33.86785,151.20732
  • Brisbane, Queensland, Australia|-27.46794,153.02809
  • Adelaide, South Australia, Australia|-34.92866,138.59863

Key Eligibility Criteria

  • Patients must be diagnosed with a solid tumor, CNS tumor or lymphoma that has progressed despite standard therapy, or for which no effective standa…
  • Age \<21 years at inclusion; patients 21 years and older may be included after approval by the Study Chair if they have a pediatric type recurrent/…
  • Patients must be enrolled on a precision medicine study (i.e. PROFYLE, ZERO or equivalent as agreed with Study Chair).
  • Patients enrolled in a Phase I cohort must have either evaluable or measurable disease.

For full eligibility, visit ClinicalTrials.gov.

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