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DAY101 vs. Standard of Care Chemotherapy in Pediatric Participants With Low-Grade Glioma Requiring First-Line Systemic Therapy (LOGGIC/FIREFLY-2)

Low-grade Glioma | Pediatric Low-grade Glioma | Rapidly Accelerated Fibrosarcoma (RAF) Altered Glioma

This is a 2-arm, randomized, open-label, multicenter, global, Phase 3 trial to evaluate the efficacy, safety, and tolerability of tovorafenib monotherapy versus standard of care (SoC) chemotherapy in participants with pediatric low-grade glioma (LGG) harboring an activating rapidly accelerated fibrosarcoma (RAF) alteration requiring first-line systemic therapy.

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Conditions de participation

  • Sexe:

    ALL
  • Âges admissibles:

    0 to 25

Critères de participation

Inclusion Criteria:

* Less than 25 years of age with LGG with known activating RAF alteration.
* Histopathologic diagnosis of glioma or glioneuronal tumor.
* At least one measurable lesion as defined by RANO criteria.
* Meet indication for first-line systemic therapy.

Exclusion Criteria:

* Participant has any of the following tumor-histological findings:

1. Schwannoma
2. Subependymal giant cell astrocytoma (Tuberous Sclerosis)
3. Diffuse intrinsic pontine glioma, even if histologically diagnosed as World Health Organization (WHO) Grade I-II
* Participant's tumor has additional pathogenic molecular alterations, including but not limited to a) isocitrate dehydrogenase (IDH) 1/2 mutation, b) Histone H3 mutation, and c) neurofibromatosis Type 1 (NF-1) loss of function alteration.
* Known or suspected diagnosis of NF-1/ neurofibromatosis Type 2 (NF-2).
* Prior or ongoing nonsurgical anticancer therapy for this indication (eg, chemotherapy, oral/IV targeted therapy) including radiation.

Lieu de l'étude

McMaster Children's Hospital
McMaster Children's Hospital
Hamilton, Ontario
Canada

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Alberta Children's Hospital
Alberta Children's Hospital
Calgary, Alberta
Canada

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Children's Hospital of Eastern Ontario
Children's Hospital of Eastern Ontario
Ottawa, Ontario
Canada

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British Columbia Children's Hospital
British Columbia Children's Hospital
Vancouver, British Columbia
Canada

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The Montreal Children's Hospital
The Montreal Children's Hospital
Montréal, Quebec
Canada

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Stollery Children's Hospital
Stollery Children's Hospital
Edmonton, Alberta
Canada

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CHU Sainte-Justine
CHU Sainte-Justine
Montréal, Quebec
Canada

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Children's Hospital London Health Sciences Centre
Children's Hospital London Health Sciences Centre
London, Ontario
Canada

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CHU Sainte-Justine
CHU Sainte-Justine
Montreal, Quebec
Canada

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The Montreal Children's Hospital
The Montreal Children's Hospital
Montreal, Quebec
Canada

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Étude parrainée par
Day One Biopharmaceuticals, Inc.
Participants recherchés
Plus d'informations
ID de l'étude: NCT05566795