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0.021709323583181 -0.0663358579263515 -0.0369548184904675 -0.000750848785583693 -0.0141028989292244 -0.00757377905458348 0.025071820318621 0.0316335857926352
Stock impact report

Annovis Announces FDA Meeting to Discuss Parkinson's Disease Dementia Program; Reaffirms FDA Alignment on Pivotal Phase 3 Alzheimer's Disease Study

Annovis Bio, Inc. (ANVS) 
Company Research Source: GlobeNewswire
MALVERN, Pa., Nov. 18, 2025 (GLOBE NEWSWIRE) -- Annovis Bio, Inc. (NYSE: ANVS) (“Annovis” or the “Company”), a late-stage clinical drug platform company pioneering transformative therapies for neurodegenerative diseases such as Alzheimer's disease (AD) and Parkinson's disease (PD), today announced that the U.S. Food and Drug Administration (FDA) has scheduled a Type C meeting in January 2026 to discuss the Company's pathway for Parkinson's disease dementia (PDD). Annovis also reaffirmed that its ongoing Phase 3 AD clinical trial continues to progress with full regulatory alignment on study design, endpoints, and patient population. "We are pleased with such proactive engagement with the FDA on our PDD program, which represents a significant opportunity to address an underserved patient population," said Maria Maccecchini, Ph.D., President and CEO. "The scheduled January meeting marks a key milestone for our pipeline, underscoring buntanetap's potential across multiple neurodegenera Show less Read more
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