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GLOBAL
Alnylam has led the translation of RNAi (RNA interference) from Nobel Prize-winning discovery into an entirely new class of medicines. In 2018, our first medicine, ONPATTRO® (patisiran), became the world’s first approved RNAi therapeutic. Our second medicine, GIVLAARI® (givosiran), was approved by the FDA in 2019. We are advancing a robust pipeline of innovative RNAi-based medicines in four therapeutic areas: genetic medicines, cardio-metabolic diseases, infectious diseases, and central nervous system (CNS) and ocular diseases.
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Updated as of July 2020
* 2 approved in the U.S., European Union, and Brazil; 1 of which is approved in Canada, Switzerland, and Japan
Patients are at the core of everything we do. Alnylam was founded to help people who lack adequate treatment options live fuller, healthier lives. Their needs drive our discoveries, and their stories further our commitment to delivering innovative therapies.
A Family Living with
hATTR Amyloidosis
Ania: Living with
Porphyria
A Family Living with
Primary Hyperoxaluria Type 1 (PH1)
Our robust pipeline contains therapies in late-stage (Phase 3) and early-stage (Phase 2 or earlier) trials. Our RNAi therapies leverage two distinct approaches to enable delivery of small interfering Ribonucleic Acid (siRNA): lipid nanoparticles (LNP) and GalNAc-conjugates.
Learn more about our investigational therapies in hereditary ATTR amyloidosis, hemophilia, hypercholesterolemia, and primary hyperoxaluria type 1.
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Learn more about our investigational therapies across multiple disease areas.
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We are growing quickly and hiring across North America, Europe, Asia, and Latin America for a wide variety of roles. We’re seeking smart, passionate, “change the world” kind of people who are ready to say, “challenge accepted” to our mission.
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