Where most other types of medicines target proteins that cause or contribute to disease after they're made, RNAi therapeutics prevent those proteins from being made in the first place.
This approach is unlocking new possibilities for treating diseases and reducing the frequency with which medicines need to be taken.
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As cutting-edge as this sounds, research into the safety and effectiveness of RNAi therapeutics is extensive and is based on over a decade of clinical trials.
The world’s first RNAi therapeutic, and Alnylam’s first commercial medicine, was approved in 2018. Since then, five other therapies have been approved in the United States and around the world.