Acadia Pharmaceuticals (ACAD)

Overall impact
B (71)

Commentary

Acadia Pharmaceuticals is a strong overall performer. With a 'B' rating of 70.7 for overall impact (83rd percentile compared to all companies), Acadia Pharmaceuticals ranks 261st out of 585 industry peers, behind Biogen, Gilead Sciences, Amgen and 257 others, and ahead of Grifols, Ionis Pharmaceuticals, Jazz Pharmaceuticals and 321 others. On top material causes for Acadia Pharmaceuticals's industry (Pharmaceuticals & Biotech), Acadia Pharmaceuticals performs well in Access to Affordable Healthcare (95.6 score), Child and Maternal Health (89.3), Child and Maternal Health (95.8) and 3 other causes where it received an 'A' score and performs poorly in Decent, Safe Work Opportunities (36.3 score) and Humane Treatment of Animals (3.3).
Impact
Cause ACAD
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Company
Employees
796
Sector
Health Care
Industry
Biotechnology
Sub-industry
Biotechnology
SASB industry
Biotechnology & Pharmaceuticals
Headquarters
Ca, United States
Share classes
ACAD
Description
ACADIA Pharmaceuticals Inc., a biopharmaceutical company, focuses on the development and commercialization of medicines for central nervous system (CNS) disorders and rare diseases in the United States. The company offers NUPLAZID (pimavanserin) for the treatment of hallucinations and delusions associated with Parkinson's disease psychosis, and DAYBUE, a novel synthetic analog of the amino-terminal tripeptide of insulin-like growth factor 1 for the treatment of Rett Syndrome. It also develops Pimavanserin, which completed Phase III clinical trial to treat the negative symptoms of schizophrenia; ACP-101, which completed Phase III clinical trial for the treatment of hyperphagia in Prader-Willi syndrome; ACP-204 that completed Phase II clinical trial for the treatment of Alzheimer's disease psychosis and Lewy Body Dementia with psychosis; ACP-711, which is in phase I clinical trial for the treatment of essential tremor; ACP-211 that is in phase I clinical trial for the treatment of treatment-resistant depression; ACP-2591 that is in Phase I development for Rett syndrome and Fragile X syndrome; and ACP-271, a GPR88 agonist used in evaluation of neurology and is in the IND-enabling stage. The company has a license agreement with Neuren Pharmaceuticals Limited to trofinetide for Rett syndrome and other indications, and a license and collaboration agreement with Stoke Therapeutics, Inc. to discover, develop, and commercialize novel RNA-based medicines for the potential treatment of severe and rare genetic neurodevelopmental diseases of the CNS. The company was formerly known as Receptor Technologies, Inc. and changed its name to ACADIA Pharmaceuticals Inc. in 1997. ACADIA Pharmaceuticals Inc. was incorporated in 1993 and is headquartered in San Diego, California.
Material causes
Ethos considers the following causes material for Acadia Pharmaceuticals, based on its industry sub-industry Biotechnology. Learn more about material causes in our methodology overview.

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