To those who say “impossible, impractical, unrealistic,” we say:

Challenge Accepted

We are developing an innovative new class of medicines called RNAi therapeutics that we believe have the potential to transform the lives of people living with rare diseases.

To those who say “impossible, impractical, unrealistic,” we say:

Challenge Accepted

We are developing an innovative new class of medicines called RNAi therapeutics that we believe have the potential to transform the lives of people living with rare diseases.

RNAi: A REVOLUTION IN BIOLOGY BUILT ON NOBEL PRIZE-WINNING RESEARCH

RNA interference (RNAi) is a breakthrough in understanding how genes are regulated in cells. It also represents a completely new approach to drug discovery and development. The 2006 Nobel Prize for Physiology or Medicine, awarded to Craig Mello and Andrew Fire, recognised the importance of RNAi as a major scientific discovery.

 

Learn More ›

Learn more about RNAi

Learn more about our research, programs, company, culture, patient stories and more.

Visit our YouTube channel ›

OUR FOCUS

Our pipeline of investigational RNAi therapeutics is focused on diseases with high unmet medical need that fall under 4 Strategic Therapeutic Areas (STArs): genetic medicines, cardio-metabolic diseases, infectious diseases, and central nervous system (CNS) and ocular diseases.

Our products approved for patients in the European Union treat hereditary ATTR (hATTR) amyloidosis with polyneuropathy, acute hepatic porphyria (AHP), primary hyperoxaluria type 1 (PH1), and hypercholesterolemia. Our therapeutic product candidates in late-stage (Phase 2 – Phase 3) development focus on hereditary ATTR (hATTR) amyloidosis, haemophilia and rare bleeding disorders and complement-mediated diseases. We have a number of early-stage programmes in development.

See our pipeline ›

career-uk-2023

JOIN OUR TEAM

As we pursue our goal of becoming a commercial organization that can independently deliver medicines to patients, we are seeking individuals with diverse skills, experiences, and backgrounds to help us build a world-class team. We are based in Cambridge, USA, with offices in Zug, Switzerland, and Maidenhead, UK, but we are also hiring throughout Europe.

View current job openings ›

CONTACT US

Alnylam UK Ltd.

Braywick Gate, Braywick Road, Maidenhead, Berkshire SL6 1DA

info@alnylam.co.uk
+44 (0) 1255 444 400

For medical information, clinical trial questions or to report an adverse event or product complaint:

Toll: +44 1628878592
Toll-free: 08001412569 (also hidden caller ID)

medinfo@alnylam.com

LEARN MORE ABOUT ALNYLAM

In-depth information about our science, our pipeline, resources for medical professionals and patients, and the latest news about Alnylam.

View lists of the past UK patient organizations that Alnylam supported in 2018, 2019, 2020, 2021 and 2022.

View the Executive Summaries for Joint Working Agreements with Alnylam UK below:

University Hospital Birmingham.

National Amyloidosis Centre - hATTR amyloidosis Therapeutic Review.

National Amyloidosis Centre - hATTR amyloidosis Genetic Counselling and Testing.

This website is intended for residents of the UK only.

Alnylam UK Ltd.

Date of prep November 2023
Corp-UK-00020