Annovis Bio (NYSE: ANVS), a late-stage clinical drug platform company developing therapies for neurodegenerative diseases, announced second-quarter 2025 results and corporate updates. The pivotal Phase 3 trial in early Alzheimer’s disease (NCT06709014) now includes 76 secured U.S. sites, with 46 actively enrolling, 38 patients dosed, and nearly 200 in screening. Enrollment is progressing on schedule with a 50% screen failure rate as expected. Recent milestones include presenting four scientific posters at AAIC 2025, hiring a director of biostatistics, hosting a trial update webcast, and securing global IP coverage for crystal buntanetap. As of June 30, 2025, cash and equivalents totaled $17.1 million, up from $10.6 million at year-end 2024. Quarterly R&D expenses were $5.2 million versus $5.8 million in the prior-year period, while G&A expenses declined to $1.1 million from $2.0 million. Net loss per share narrowed to $0.32 from $0.44.
To view the full press release, visit https://ibn.fm/iO1TH
About Annovis Bio Inc.
Headquartered in Malvern, Pennsylvania, Annovis is dedicated to addressing neurodegeneration in diseases such as AD and PD. The Company is committed to developing innovative therapies that improve patient outcomes and quality of life. For more information, visit www.annovisbio.com and follow us on LinkedIn , YouTube , and X .
NOTE TO INVESTORS: The latest news and updates relating to ANVS are available in the company’s newsroom at https://ibn.fm/ANVS
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