Alnylam Pharmaceuticals (ALNY)

Overall impact
B (75)

Commentary

Alnylam Pharmaceuticals is a strong overall performer. With a 'B' rating of 75.0 for overall impact (89th percentile compared to all companies), Alnylam Pharmaceuticals ranks 146th out of 585 industry peers, behind Biogen, Amgen, Regeneron Pharmaceuticals and 142 others, and ahead of Grifols, Ionis Pharmaceuticals, Gilead Sciences and 436 others. On top material causes for Alnylam Pharmaceuticals's industry (Pharmaceuticals & Biotech), Alnylam Pharmaceuticals performs well in Disease Eradication (96.5 score), Child and Maternal Health (96.0), Improved Mental Health (81.6) and 5 other causes where it received an 'A' score and performs poorly in Disaster Readiness and Effective Aid (39.3 score) and Humane Treatment of Animals (3.3).
Impact
Cause ALNY
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Company
Founded
2002
Employees
2,230
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, and commercializes therapeutics based on ribonucleic acid interference. It offers ONPATTRO and AMVUTTRA for hereditary transthyretin-mediated amyloidosis; GIVLAARI for acute hepatic porphyria; OXLUMO for primary hyperoxaluria type 1; and Leqvio for hypercholesterolemia. It also develops vutrisiran, which is in phase III clinical trial for transthyretin amyloidosis (ATTR) with cardiomyopathy; Nucresiran that is in phase I clinical trial for ATTR amyloidosis; Fitusiran, which is in phase III clinical trial for hemophilia; cemdisiran that is in phase III clinical trial for Myasthenia Gravis and paroxysmal nocturnal hemoglobinuria, and geographic atrophy; and ALN-6400, which is in phase I clinical trial for bleeding disorders. In addition, the company is also developing Zilebesiran, which is in phase II clinical trial for hypertension; Rapirosiran that is in phase II clinical trial for Metabolic dysfunction-associated steatohepatitis; ALN-4324, which is in phase I clinical trial for type 2 diabetes mellitus; ALN-PNP that is in phase I clinical trial for non-alcoholic fatty liver disease; ALN-APOC3, which is in phase I clinical trial for dyslipidemia; Mivelsiran that is in phase II clinical trial for cerebral amyloid angiopathy, and phase I clinical trial for Alzheimer's disease; and ALN-HTT02 that is in phase I clinical trial for Huntington's disease. Further, it develops ALN-SOD, which is in phase II clinical trial for SOD1 Amyotrophic lateral sclerosis; Elebsiran that is in phase II clinical trial for Hepatitis B and D virus infections; ALN-BCAT that is in phase I clinical trial for hepatocellular carcinoma; and ALN-ANG3. It has collaborations with Regeneron Pharmaceuticals, Inc.; Roche Holding AG; Regeneron Pharmaceuticals, Inc.; Sanofi S.A.; Novartis AG; PeptiDream, Inc; Dicerna Pharmaceuticals, Inc.; and Ionis Pharmaceuticals, Inc. The company 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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