Alnylam Pharmaceuticals (ALNY)

Overall impact
B (73)

Commentary

Alnylam Pharmaceuticals is a strong overall performer. With a 'B' rating of 73.5 for overall impact (86th percentile compared to all companies), Alnylam Pharmaceuticals ranks 69th out of 262 industry peers, behind Assembly Biosciences, Piramal Enterprises, Evoke Pharma and 65 others, and ahead of Catalyst Pharmaceuticals, Agios Pharmaceuticals, Pharmaron Beijing H and 190 others. On top material causes for Alnylam Pharmaceuticals's industry (Pharmaceuticals), Alnylam Pharmaceuticals performs well in Child and Maternal Health (84.7 score), Child and Maternal Health (84.7), Child and Maternal Health (95.0) and 60 other causes where it received an 'A' score and performs poorly in Accountable Institutions (29.2 score), Sustainable Use of Water (37.0), Accountable Institutions (29.2) and 12 other causes where it received a 'D' or 'F' score.
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Company
Founded
2002
Employees
2,500
Sector
Health Care
Industry
Pharmaceuticals
Sub-industry
Pharmaceuticals
SASB industry
Biotechnology & Pharmaceuticals
Headquarters
Ma, United States
Share classes
ALNY
Mission
Dedicated to proving that innovative science, perseverance, and passion can come together to improve the lives of patients.
Description
Alnylam Pharmaceuticals, Inc. discovers, develops, manufactures, and commercializes therapeutics based on ribonucleic acid interference in the United States, Europe, and internationally. The company offers ONPATTRO for hereditary transthyretin-mediated (hATTR) amyloidosis; AMVUTTRA for ATTR and hATTR amyloidosis; Leqvio for hypercholesterolemia; Qfitlia for hemophilia A or B; GIVLAARI for acute hepatic porphyria; and OXLUMO for primary hyperoxaluria type 1. It also develops a range of products in Phase 3 trial, such as Nucresiran for ATTR amyloidosis; Zilebesiran for hypertension; Cemdisiran for myasthenia gravis, paroxysmal nocturnal hemoglobinuria, and geographic atrophy; and Elebsiran for hepatitis D virus infections. In addition, the company is developing various products in Phase 2 trial, including Rapirosiran for metabolic dysfunction-associated steatohepatitis; ALN-ANG3 for diabetic kidney disease; ALN-4324 for type 2 diabetes mellitus; Mivelsiran for cerebral amyloid angiopathy, as well as in Phase 1 trial for Alzheimer's disease; and ALN-6400 for bleeding disorders. Further, it develops a range of products in Phase 1 trial, such as ALN-2232 for obesity and weight management; ALN-PNP for non-alcoholic fatty liver disease; ALN-APOC3 for dyslipidemia; ALN-CIDEB for metabolic dysfunction-associated steatohepatitis; ALN-HTT02 for Huntington's disease; ALN-5288 for Alzheimer's disease; ALN-SOD for SOD1 amyotrophic lateral sclerosis; ALN-SNCA for Parkinson's disease; AG-236 for polycythemia vera; ALN-CFB for paroxysmal nocturnal hemoglobinuria; ALN-BCAT for hepatocellular carcinoma; and ALN-4285, ALN-4915, and ALN-F1202 for healthy volunteers. The company has collaborations with Regeneron Pharmaceuticals, Inc.; Roche Holding AG; Sanofi S.A.; Novartis AG; PeptiDream, Inc; Dicerna Pharmaceuticals, Inc.; and Ionis Pharmaceuticals, Inc. Alnylam Pharmaceuticals, Inc. was founded in 2002 and is headquartered in Cambridge, Massachusetts.
Material causes
Ethos considers the following causes material for Alnylam Pharmaceuticals, based on its industry sub-industry Pharmaceuticals. Learn more about material causes in our methodology overview.

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