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tovorafenib

Generic: TOVORAFENIB·Brand: OJEMDA, Ojemda

tovorafenib: 6 clinical trials tracked.

tovorafenib evidence translation

What we can confirm

6 tracked trials

No verified listed company relationship

What it means

AI will separate confirmed drug evidence from unknown company context.

What to watch

Watch trial status, endpoints, and the next source-backed update.
BioSniper AIPage evidence connected

Prepared research question

What is verified about tovorafenib, and what remains unknown?

Run cited research

Traceable citations · Unknowns marked

See linked entities and source evidence8 indications · 1 study sponsors
Clinical Trial Registry Records (6)

A Phase 2 Study of Tovorafenib in Pediatric and Young Adult Patients Newly Diagnosed With High-Grade Glioma (HGG), Including Diffuse Intrinsic Pontine Glioma (DIPG), Which Harbor Alterations in the Mitogen-Activated Protein Kinase (MAPK) Pathway

NCT07206849Registry updated 2026-04-08·Phase 2
Not yet recruiting

Primary endpoint: Progression Free Survival Stratum A

Interventionalopen79 targetStarted 2026-05Completion 2037-05Nationwide Children's Hospital

LOGGIC/FIREFLY-2: A Phase 3, Randomized, International Multicenter Trial of DAY101 Monotherapy Versus Standard of Care Chemotherapy in Patients With Pediatric Low-Grade Glioma Harboring an Activating RAF Alteration Requiring First-Line Systemic Therapy

NCT05566795Registry updated 2026-05-14·Phase 3·DAWN
Active, not recruiting

Primary endpoint: Objective response rate (ORR) of tovorafenib monotherapy versus SoC chemotherapy

InterventionalRandomizedopen418 targetStarted 2023-02Completion 2031-0650 sites · Australia, Austria, Belgium, Brazil…Day One Biopharmaceuticals, Inc.

Tovorafenib for the Treatment of Newly Diagnosed or Recurrent Craniopharyngioma in Children and Young Adults

NCT05465174Registry updated 2026-04-23·Phase 2
Recruiting

Primary endpoint: Progression free survival rate (PFS)

Interventionalopen57 targetStarted 2022-09Completion 2028-0320 sites · Australia, United StatesSabine Mueller, MD, PhD

A Phase 1b/2, Subprotocol of DAY101 in Combination With Pimasertib for Patients With Recurrent, Progressive, or Refractory Solid Tumors and MAPK Pathway Aberrations

NCT07121829Registry updated 2025-08-14·Phase 1·DAWN
Terminated

Primary endpoint: Number of participants who will report Treatment emergent adverse events (TEAEs) and serious TEAEs

Interventionalopen44 targetStarted 2022-05Completion 2024-1210 sites · Canada, United StatesDay One Biopharmaceuticals, Inc.

A Phase 2, Subprotocol of DAY101 Monotherapy for Patients With Recurrent, Progressive, or Refractory Solid Tumors With MAPK Pathway Aberrations

NCT04985604Registry updated 2025-10-02·Phase 2·DAWN
Terminated

Primary endpoint: Overall Response Rate (ORR) by the Investigator

Interventionalopen23 targetStarted 2021-07Completion 2024-0720 sites · Australia, Belgium, Canada, France…Day One Biopharmaceuticals, Inc.

FIREFLY-1: A Phase 2, Open-Label, Multicenter Study to Evaluate the Safety and Efficacy of the Oral Pan-RAF Inhibitor DAY101 in Pediatric Patients With RAF-Altered, Recurrent or Progressive Low-Grade Glioma and Advanced Solid Tumors

NCT04775485Registry updated 2025-04-10·Phase 2·DAWN
Recruiting

Primary endpoint: Arm 1: Overall response rate

Interventionalopen141 targetStarted 2021-04Completion 2027-0535 sites · Australia, Canada, Denmark, Germany…Day One Biopharmaceuticals, Inc.