Alemtuzumab
Brand names: Lemtrada, MabCampath
A humanised anti-CD52 monoclonal antibody used as a disease-modifying therapy for highly active relapsing-remitting multiple sclerosis.
ClinCalc Pro is rebuilding its dose data from primary open sources — the manufacturer SmPC (eMC), the WHO Model Formulary and other official references — under clinician review. This drug's structured dose is not yet published here. Confirm all doses against the product SmPC and your local formulary before prescribing.
Clinical monograph
How it works
It binds CD52 on lymphocytes causing antibody-dependent cell lysis and profound depletion, followed by immune reconstitution that is thought to reduce inflammatory disease activity.
Prescribing in practice
- It carries serious risks including secondary autoimmune disorders (notably thyroid disease, immune thrombocytopenia and anti-GBM nephropathy), serious infusion reactions, stroke and cardiovascular events, so MHRA-mandated restrictions, premedication and a long-term monthly monitoring programme apply.
- Use is restricted to specified relapsing multiple sclerosis populations under specialist neurology supervision with a controlled-access and monitoring scheme.
- Antiviral and other infection prophylaxis is required around treatment courses, with screening for latent infections beforehand.
Monitoring
Perform monthly blood and urine monitoring (including full blood count, renal function and urinalysis) and periodic thyroid function tests for several years after the last course.
Counselling the patient
- Continue the monthly blood and urine tests for years after treatment even when you feel well.
- Report symptoms such as easy bruising or bleeding, neck swelling, dark urine or signs of infection promptly.
- Seek urgent care for chest pain, severe headache or sudden weakness shortly after an infusion.
Evidence & guidelines
Use is informed by the CARE-MS trials and is subject to MHRA risk-minimisation measures restricting its indication.
Reference: ABN MS prescribing 2024; MHRA DSU April 2020; SmPC Lemtrada; Drug verified in RxNorm (NLM); confirm dosing against the manufacturer SPC (eMC). Verify against your local formulary and current prescribing references before prescribing. Monograph status: clinician-reviewed (2026-07-04).
Related
Curated clinical cross-links plus same-class fallbacks.
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