Maia Biotechnology Inc. announced a business update highlighting key achievements in 2025 and outlining targeted milestones for 2026. The company reported strong clinical execution in 2025, delivering efficacy data for ateganosine, its telomere-targeting anticancer agent, sequenced with a checkpoint inhibitor in third-line non-small cell lung cancer (NSCLC). Results showed disease control, response rates, and survival data exceeding standard of care benchmarks. Ateganosine received FDA Fast Track designation in 2025, supporting concurrent Phase 2 and Phase 3 trials and positioning the drug for potential Accelerated Approval and Priority Review. Maia Biotechnology also established combination partnerships with Roche for atezolizumab and BeOne Medicines for tislelizumab. The company raised approximately $17.6 million in capital during 2025, with board members participating in nearly all transactions. As of December 31, 2025, directors and officers collectively hold more than 5 million shares, representing approximately 13% of the company. Ateganosine remains the only direct telomere-targeting anticancer agent in clinical development, with anticipated early commercial approval within 18 to 24 months.
Disclaimer: This news brief was created by Public Technologies (PUBT) using generative artificial intelligence. While PUBT strives to provide accurate and timely information, this AI-generated content is for informational purposes only and should not be interpreted as financial, investment, or legal advice. Maia Biotechnology Inc. published the original content used to generate this news brief via GlobeNewswire (Ref. ID: GNW9628149-en) on January 20, 2026, and is solely responsible for the information contained therein.
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