Maia Biotechnology Inc. published a 2026 shareholder letter highlighting updates on ateganosine (THIO) clinical development in non-small cell lung cancer. The letter cites interim Phase 2 THIO-101 results of 88% disease control rate, 38% overall response rate, and 17.8 months median overall survival, and notes FDA Fast Track designation granted in July 2025. The letter also states Phase 3 THIO-104 is underway with up to 300 patients planned and indicates Phase 2 THIO-101 Part C is nearing completion with a potential accelerated approval pathway. The full letter can be accessed through the link below.
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