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206,087 Results for "pediatric brain tumor foundation".
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Ursula Burns, former Xerox CEO, and Jordan Wertlieb, EVP and COO of Hearst, appointed to the Pediatric Brain Tumor Foundation’s Advisory Board as inaugural members
The Pediatric Brain Tumor Foundation announced the appointment of Ursula Burns and Jordan Wertlieb as inaugural members of the organization’s new Advisory Board.
June 25, 2024
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5 min read
Press Releases
The Pediatric Brain Tumor Foundation welcomes Day One Biopharmaceuticals’ renowned Dr. Samuel C. Blackman to its Board of Directors
January 31, 2025
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4 min read
Press Releases
U.S. Food and Drug Administration Approves FoundationOne®CDx as a Companion Diagnostic for OJEMDA™ (tovorafenib) to Treat the Most Common Form of Childhood Brain Tumor in Pediatric Patients
January 17, 2025
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5 min read
Press Releases
CBTN Partners with Day One to Drive New Therapies for Pediatric Brain Tumors
December 17, 2024
·
2 min read
Press Releases
Treovir and Matica Bio Forms Strategic Partnership to Advance Innovative Therapies for Pediatric Brain Tumors
December 4, 2024
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3 min read
FDA
PNOC Foundation, a Leading Non-profit to Further Advancements in Pediatric Brain Cancer, Announces FDA Approval of Tovorafenib (Day101) in Partnership With PNOC Scientific Consortium and Day One Biopharmaceuticals
The Pediatric Neuro-Oncology Consortium Foundation, a platinum rated non-profit dedicated to supporting advancements in childhood brain cancer research and clinical trials, announces the FDA approval of Tovorafenib, a significant advancement in the fight against pediatric low-grade glioma brain tumors.
April 24, 2024
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3 min read
Press Releases
GT Medical Technologies Announces Launch of GammaTile® Center of Excellence Program and First Designation, USC Brain Tumor Center
April 9, 2025
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3 min read
Press Releases
BrainChild Bio, Inc. to Clinically Advance BCB-276, an Autologous B7-H3 Targeting CAR T-cell Therapy for Incurable Pediatric Brain Tumors
January 7, 2025
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5 min read
FDA
Day One’s Ojemda Gets FDA Accelerated Approval for Pediatric Brain Tumor
The FDA on Tuesday approved Day One Biopharmaceuticals’ type II RAF inhibitor Ojemda, which is designed to penetrate the blood-brain barrier, for the treatment of relapsed or refractory pediatric low-grade glioma.
April 24, 2024
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2 min read
·
Tristan Manalac
Press Releases
TippingPoint Biosciences Closes New Funding to Support Drug for Rare Pediatric Brain Tumor
September 4, 2024
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5 min read
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