ANVS

FDA Accepts Final Protocol For Annovis Bio's Pivotal Phase 3 Alzheimer's Disease Study

(RTTNews) - Annovis Bio, Inc. (ANVS), a clinical-stage biotechnology company, announced on Tuesday that the FDA has accepted its updated protocol for the pivotal Phase 3 Alzheimer's Disease or AD study, set to begin in January 2025.

The new protocol consolidates the original plan for two separate trials into a single 6/18-month study.

The first 6 months will focus on symptomatic effects, while the subsequent 12-month period will assess the disease-modifying potential of buntanetap.

This streamlined approach accelerates the timeline for development while ensuring scientific rigor. The 6-month symptomatic data could support a New Drug Application (NDA) filing, with the full study continuing to evaluate the long-term impact on disease progression.

Maria Maccecchini, CEO of Annovis Bio, expressed excitement over the design, saying it brings them closer to providing a novel treatment for patients with early-stage Alzheimer's disease.

Currently, ANVS is trading at $5.14 down by 5.14%.

The views and opinions expressed herein are the views and opinions of the author and do not necessarily reflect those of Nasdaq, Inc.

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