Quince Therapeutics Inc. announced a positive outcome from a pre-planned safety analysis conducted by an independent data and safety monitoring board (iDSMB) for its ongoing pivotal Phase 3 NEAT clinical trial. The study is evaluating encapsulated dexamethasone sodium phosphate (eDSP) in patients with Ataxia-Telangiectasia (A-T). The iDSMB identified no safety concerns and recommended that the trial continue without modifications. The Phase 3 NEAT study is a randomized, double-blind, placebo-controlled trial assessing the neurological effects of eDSP. Topline results from the study are expected to be reported in the first quarter of 2026.
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. Quince Therapeutics Inc. published the original content used to generate this news brief via Business Wire (Ref. ID: 20251021956399) on November 10, 2025, and is solely responsible for the information contained therein.
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