Quince Therapeutics Inc. announced topline results from its pivotal Phase 3 NEAT clinical trial evaluating dexamethasone sodium phosphate encapsulated in autologous erythrocytes (eDSP) in patients with Ataxia-Telangiectasia (A-T). The trial did not achieve statistical significance for its primary and key secondary endpoints. eDSP was generally well tolerated, with no clinically meaningful safety concerns identified. Quince Therapeutics will cease clinical development of eDSP and intends to preserve cash and explore available options. The company has already presented these results.
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: 20260129349326) on January 29, 2026, and is solely responsible for the information contained therein.
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