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US Congress Extends Rare Pediatric Disease Voucher Program to 2029, Boosting Neuren’s Prospects

The US Congress has reauthorized the Rare Pediatric Disease Priority Review Voucher program through September 2029, a move that could significantly benefit Neuren Pharmaceuticals as it advances its rare disease drug candidates.
Ada Torres
5 Feb 2026

Neuren Advances NNZ-2591 with FDA Guidance for Rare Neurological Disorders

Neuren Pharmaceuticals has received detailed feedback from the US FDA on its clinical development plans for NNZ-2591 targeting hypoxic ischemic encephalopathy and Pitt Hopkins syndrome, paving a clearer path forward despite some delays.
Ada Torres
4 Feb 2026

Acadia Faces Setback in EU Approval for Rett Syndrome Drug Trofinetide

Acadia Pharmaceuticals has received a negative vote from the European Medicines Agency’s committee on its application to market trofinetide for Rett syndrome in the EU, prompting plans for a re-examination request.
Victor Sage
3 Feb 2026

Healthcare Wrap - Week 4 (19 Jan -> 23 Jan) 2026

A small-cap healthcare rally had a clear centre: distribution deals, US regulatory steps, and big cheques. Osteopore, Echo IQ and Anteris led the week, while a handful of names slipped despite solid operational updates.
Logan Eniac
25 Jan 2026

Neuren Confirms DAYBUE Sales Projection Could Boost Royalties to $700m by 2028

Neuren Pharmaceuticals has affirmed the material impact of Acadia’s projection that DAYBUE global net sales could reach approximately US$700 million by 2028, underpinning its royalty revenue outlook.
Ada Torres
19 Jan 2026

Neuren’s DAYBUE Set to Hit US$700m Sales by 2028 with New US and Global Growth

Neuren Pharmaceuticals’ partner Acadia projects DAYBUE sales to reach around US$700 million by 2028, driven by US market expansion and international approvals. The launch of a new formulation and ongoing clinical trials in Japan underpin this optimistic outlook.
Ada Torres
14 Jan 2026

Neuren Advances PMS Treatment with Published Phase 2 Trial and Ongoing Phase 3 Recruitment

Neuren Pharmaceuticals has published promising Phase 2 trial results for NNZ-2591 in Phelan-McDermid syndrome, underpinning its ongoing Phase 3 Koala trial recruiting in the US.
Ada Torres
7 Jan 2026

Health Canada Greenlights Neuren’s Phase 3 Trial for Rare Syndrome Drug

Neuren Pharmaceuticals has secured Health Canada approval to expand its pivotal Phase 3 trial of NNZ-2591 for Phelan-McDermid syndrome into Canadian sites, complementing ongoing US enrolment.
Ada Torres
22 Dec 2025

FDA Greenlights DAYBUE STIX Powder for Rett Syndrome, Boosting Neuren Royalties

Neuren Pharmaceuticals’ partner Acadia secures FDA approval for DAYBUE STIX, a new powder formulation of trofinetide offering greater flexibility for Rett syndrome patients. This milestone expands treatment options and sets the stage for increased royalty revenue in 2026.
Victor Sage
15 Dec 2025

Neuren Hits Record DAYBUE Sales, Royalty Income Surges 24% in Q3 2025

Neuren Pharmaceuticals reported a milestone quarter with DAYBUE net sales reaching US$101.1 million, driving a 24% jump in royalty income. The expanding patient base and community physician uptake signal strong growth ahead.
Victor Sage
6 Nov 2025

FDA Fast Tracks Neuren’s NNZ-2591 for Phelan-McDermid Syndrome

Neuren Pharmaceuticals has secured FDA Fast Track designation for its drug NNZ-2591 targeting Phelan-McDermid syndrome, accelerating its path through clinical development. This milestone underscores the urgent need for treatments in rare neurodevelopmental disorders.
Ada Torres
20 Oct 2025

Neuren Pharmaceuticals Posts 88% Profit Surge, Advances NNZ-2591 Phase 3 Trial

Neuren Pharmaceuticals reported a robust half-year with an 88% increase in net profit, driven by rising royalties from DAYBUE™ sales and progress in its NNZ-2591 clinical program. The company also completed a $39.6 million share buy-back, underscoring confidence in its growth trajectory.
Ada Torres
27 Aug 2025