Arrowhead Pharmaceuticals (ARWR)

Overall impact
C (59)

Commentary

Arrowhead Pharmaceuticals is an average overall performer. With a 'C' rating of 59.2 for overall impact (61st percentile compared to all companies), Arrowhead Pharmaceuticals ranks 424th out of 585 industry peers, behind Biogen, Ionis Pharmaceuticals, Gilead Sciences and 420 others, and ahead of Grifols, Jazz Pharmaceuticals, Bluebird Bio and 158 others. On top material causes for Arrowhead Pharmaceuticals's industry (Pharmaceuticals & Biotech), Arrowhead Pharmaceuticals performs well in Technology Innovation (92.6 score) and Disease Eradication (96.4) and performs poorly in Accountable Institutions (35.6 score), Equal Pay and Opportunity (36.1), Humane Treatment of Animals (3.3) and 2 other causes where it received a 'D' or 'F' score.
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Cause ARWR
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Company
Employees
711
Sector
Health Care
Industry
Biotechnology
Sub-industry
Biotechnology
SASB industry
Biotechnology & Pharmaceuticals
Headquarters
Ca, United States
Share classes
ARWR
Description
Arrowhead Pharmaceuticals, Inc. develops medicines for the treatment of intractable diseases in the United States. The company's product pipeline includes Plozasiran, which has completed Phase 3 clinical trial to treat hypertriglyceridemia, dyslipidemia, and familial chylomicronemia syndrome; Olpasiran that is in Phase 3 clinical trial to reduce the production of apolipoprotein A; and Fazirsiran that is in Phase 3 clinical trial for the treatment of liver disease associated with alpha-1 antitrypsin deficiency. It also develops Zodasiran that is in Phase 2b clinical trial for the treatment of dyslipidemia and hypertriglyceridemia; GSK-4532990 to treat metabolic-dysfunction associated steatohepatitis (MASH); and Daplusiran/Tomligisiran which is in Phase 2 clinical trial for the treatment of Chronic Hepatitis B. In addition, the company is developing ARO-PNPLA3, which is in Phase 1 clinical trial to treat patients with MASH; ARO-INHBE to reduce the hepatic expression of the INHBE gene and its secreted gene product; ARO-RAGE to treat inflammatory lung disease; ARO-MUC5AC to treat muco-obstructive pulmonary diseases; and ARO-MMP7 for the treatment of idiopathic pulmonary fibrosis that is in Phase 1/2a clinical trials. Further, it develops ARO-DUX4 for the treatment of facioscapulohumeral muscular dystrophy; ARO-DM1 to treat patients with Type 1 Myotonic Dystrophy; ARO-C3 to treat complement-mediated renal disease; ARO-CFB for the treatment of complement-mediated kidney disease that is in Phase 1/2a clinical trial; and ARO-ATXN2 for the treatment of Spinocerebellar Ataxia Type 2 that is in Phase 1 clinical trial. Arrowhead Pharmaceuticals, Inc. has collaboration and license agreements with Glaxosmithkline Intellectual Property (No. 3) Limited; Horizon Therapeutics Ireland DAC; Takeda Pharmaceutical Company Limited; and with Amgen Inc. The company was founded in 2003 and is headquartered in Pasadena, California.
Material causes
Ethos considers the following causes material for Arrowhead Pharmaceuticals, based on its industry sub-industry Biotechnology. Learn more about material causes in our methodology overview.

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