Welcome to our dedicated page for Acadia Pharmaceuticals news (Ticker: ACAD), a resource for investors and traders seeking the latest updates and insights on Acadia Pharmaceuticals stock.
News and updates for Acadia Pharmaceuticals Inc. (NASDAQ: ACAD) focus on its activities in neurological and rare diseases, including commercial performance and clinical development. Company press releases highlight revenue trends from its marketed medicines NUPLAZID for hallucinations and delusions associated with Parkinson’s disease psychosis and DAYBUE for Rett syndrome, as well as guidance ranges for total revenues and net product sales.
Investors following ACAD news can see announcements of quarterly financial results, participation in major healthcare and investor conferences, and business updates presented at events such as the J.P. Morgan Healthcare Conference. These updates often describe how NUPLAZID and DAYBUE are performing commercially and how Acadia views the growth outlook for its neurology and neuro‑rare franchises.
Acadia’s news flow also covers regulatory and clinical milestones. Examples include U.S. Food and Drug Administration approval of DAYBUE STIX, a powder formulation of trofinetide for oral solution for Rett syndrome in adults and pediatric patients 2 years of age and older, approval of DAYBUE oral solution by the Ministry of Health in Israel, and progress toward regulatory opinions and late‑stage studies for trofinetide in other regions. The company issues updates on its pipeline, such as timelines for Phase 2 and Phase 3 trials of remlifanserin (ACP‑204) in Alzheimer’s disease psychosis and Lewy body dementia psychosis, and data presentations on ACP‑711 and NUPLAZID at scientific congresses.
Readers of this ACAD news page can use it to track Acadia’s financial disclosures, regulatory approvals, clinical trial readouts, and strategic commentary from management over time. The news archive provides context on how the company’s commercial portfolio and pipeline in central nervous system and neuro‑rare diseases are evolving.
Acadia Pharmaceuticals (Nasdaq: ACAD) will present new analyses of pimavanserin clinical data for dementia-related psychosis at the 13th Clinical Trials on Alzheimer's Disease Conference (CTAD) from November 4-7, 2020. Presentations will cover the impact of pimavanserin on cognition and motor function in neurodegenerative conditions, alongside safety assessments. Notable presentations include findings from the Phase 3 HARMONY Study and a literature review on antipsychotic treatments for dementia-related psychosis. The FDA accepted Acadia's supplemental application for pimavanserin in this indication, with a PDUFA date set for April 3, 2021.
Acadia Pharmaceuticals (ACAD) plans to report its third-quarter financial results on November 4, 2020, after market close. A conference call will follow at 4:30 PM ET to discuss the results. Participants can access the call via various numbers provided for U.S. and international callers. The call will also be available as a live webcast on Acadia's website, which will remain archived until December 2, 2020. Acadia focuses on neuroscience breakthroughs, notably the only approved therapy for Parkinson's disease psychosis, and is exploring treatments for other neuropsychiatric conditions.
Acadia Pharmaceuticals and the Lewy Body Dementia Association have announced a partnership to produce an educational adaptation of the film Robin's Wish. This new version, titled SPARK - Robin Williams and his Battle with Lewy Body Dementia, aims to increase awareness and educate healthcare professionals about Lewy body dementia (LBD), which affects 1.4 million people in the U.S. The film will be available in late October for academic institutions to aid in outreach and education on LBD symptoms and management.