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The United Kingdom

Alexion Mission

Pioneering New Possibilities for the Rare Disease Community 

We are driven by a mission to change what it means to live with a rare disease. Built on a legacy of turning pioneering science into transformative treatments, we listen to and partner with the rare disease ecosystem to help improve outcomes for more people impacted by rare diseases across the globe.

Developing breakthrough therapies for rare diseases is only possible because of the tireless efforts of our global community of researchers and scientists, advocates and caregivers, and most important, patients.

As part of AstraZeneca, we have the potential to impact the lives of even more people around the world.

Rare Diseases Supported in the UK

Alexion works across various rare diseases, including:

Paroxysmal Nocturnal Haemoglobinuria (PNH)

A rare, chronic, progressive and potentially life-threatening blood disorder. It is characterised by red blood cell destruction within blood vessels (also known as intravascular haemolysis) and white blood cell and platelet activation, which can result in thrombosis (blood clots).

Atypical Haemolytic Uraemic Syndrome (aHUS)

A rare disease that can cause progressive injury to vital organs, primarily the kidneys, via damage to the walls of blood vessels and blood clots.

Neurofibromatosis Type 1 (NF1) Plexiform Neurofibromas (PN)

A rare, progressive, genetic condition characterized by non-malignant (non-cancerous) tumors called plexiform neurofibromas (PN) that develop in the brain, and along the spinal cord and nerve.

Generalised Myasthenia Gravis (gMG)

A rare, autoimmune neuromuscular disease characterised by loss of muscle function and severe muscle weakness.

Neuromyelitis Optica Spectrum Disorder (NMOSD)

A rare autoimmune disease of the central nervous system, characterised by unpredictable relapses which can result in cumulative disability.

Hypophosphatasia (HPP)

A rare, inherited, metabolic disease characterized by impaired mineralization (“calcification”), the process that hardens and strengthens bones and teeth. This can lead to poor growth and development, weakness and deformity of bones and other skeletal abnormalities, and premature loss of teeth with the root intact.

Lysosomal Acid Lipase Deficiency (LAL-D)

A genetic, and progressive ultra-rare metabolic disease associated with multiorgan damage in infant, paediatric and adult patients, and premature death in infants.

Clinical Trials

Clinical Trials

Alexion is committed to serving people affected by rare diseases through the discovery, development and delivery of life-changing medicines. Our goal is to bring safe and effective medicines to as many patients as possible by conducting rigorous clinical trials and obtaining marketing approval by regulatory authorities around the world. Our work is marked by a commitment to the highest standards of preclinical and clinical research, and an acute sense of urgency. As such, we prioritize access to our investigational medicines through participation in a clinical trial.

Transparency and Disclosure

Alexion is committed to operating with integrity, accountability, and transparency, and to complying with all applicable laws and regulations. Alexion fully participates in the Association of British Pharmaceutical Industry’s (ABPI) Disclosure UK initiative, to increase transparency about the relationships we have with doctors, nurses, pharmacists, and other healthcare professionals.

Careers

Career Opportunities

Uniting our teams driven by our commitment to pioneer life-changing outcomes for the rare disease community and the health systems we operate in.

At Alexion, we foster an environment that attracts and retains the best talent.

Alexion Pharma UK Ltd

Customer Operations - Customer Order queries

6th Floor
2 Pancras Square London,
N1C 4AG

UK 0800 1300 212

Veeva ID: M/UK/UNB-U/0495

Date of Preparation: March 2026