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Neuren Pharmaceuticals Limited (NEU) investor relations material
Neuren Pharmaceuticals Limited Investor Presentation summary
Complete event summary combining all related documents: earnings call transcript, report, and slide presentation.Strategic focus and pipeline
Focus on neurodevelopmental disorders with severe unmet needs, including Rett, Fragile X, Phelan-McDermid, Pitt Hopkins, Angelman, Prader-Willi, SYNGAP1-related disorders, and Hypoxic-Ischemic Encephalopathy (HIE).
NNZ-2591 is being developed as a multi-indication platform, with Phase 3 trials underway for Phelan-McDermid and advancing in Pitt Hopkins and HIE.
Trofinetide (Daybue®) is commercialized for Rett syndrome, with global expansion ongoing.
Orphan Drug and Rare Pediatric Disease designations secured for key programs.
Pipeline includes multiple late-stage and registration-phase assets.
Financial performance and commercial outlook
$490 million income from Daybue® in 2023 to date, with $310 million cash as of September 2025.
Royalty income from Daybue® projected at A$63-66 million in 2025, based on US net sales guidance of $385-400 million.
Tiered royalties from Acadia partnership range from mid-teens to low-20s percent of net sales, with significant milestone payments for US, Europe, and Japan.
Record number of active Daybue® patients in Q3 2025, with 74% of new prescriptions from outside centers of excellence.
Share buyback of A$50 million completed in 2025.
Market expansion and growth drivers
US Rett patient base expanded to 5,500-5,800 diagnosed, with theoretical prevalence up to 9,000.
Global expansion includes Canada (approved), Europe (MAA filed, opinion expected Q1 2026), Japan (Orphan Drug status, clinical trial underway), and named patient programs in other regions.
Key growth drivers: increasing diagnosis, therapy initiation, and patient persistency rates.
Acadia field force expanded by 30% in 2025 to support Daybue® uptake.
Substantial market opportunities in PMS, PTHS, and HIE, with tens of thousands of potential patients globally.
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