Orbus Therapeutics Announces Oral Presentation Of Updated Results With Blinded Independent Central Review From The Phase 3 STELLAR Clinical Trial At The Society For Neuro-Oncology Annual Meeting
SNO presentation information:
Title: Updated results of Phase 3 STELLAR trial: Eflornithine improves overall survival and blinded independent central review determined progression free survival in patients with recurrent WHO 2021 grade 3 IDH-mutant astrocytoma
Date and Time: Saturday, November 22, 2025, 11:09 a.m.–11:14 a.m.
Session Name: Clinical Trial Abstracts - Session II
Presenter: Howard Colman, MD, PhD, FAAN, the Jon M. Huntsman Presidential Chair in Neuro-Oncology at the Huntsman Cancer Institute at the University of Utah
Abstract Number: CTNI-58
Location: Hawaii Convention Center, Lili'u Theater 310
About Eflornithine
Eflornithine is a novel cytostatic agent that irreversibly inhibits ornithine decarboxylase, a key enzyme in mammalian polyamine biosynthesis that is upregulated in certain types of cancer. Eflornithine has been granted Orphan Drug Designation and Breakthrough Therapy Designation for the treatment of patients with anaplastic glioma by the U.S. Food and Drug Administration (FDA) and has also been granted Orphan Medicinal Product status for the treatment of glioma by the Committee for Medicinal Products for Human Use (CHMP) at the European Medicines Agency (EMA).
About Orbus Therapeutics
Orbus Therapeutics Inc. is a late-stage, private biopharmaceutical company that is dedicated to developing products that treat rare diseases for which there are few, if any, effective therapies. The Company's lead product candidate, eflornithine, has completed one Phase 3 clinical study in patients with recurrent anaplastic astrocytoma, a rare form of central nervous system cancer. For more information, please visit the Company's website at .

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