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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