Anpheros Search · Treatment

Alemtuzumab

Also known as: Lemtrada · Campath

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In short

In the European Union, alemtuzumab is indicated for adult patients with relapsing-remitting multiple sclerosis with active disease defined by clinical or imaging features. In the United States, it is indicated as a single agent for the treatment of B-cell chronic lymphocytic leukemia. Alemtuzumab is listed by the cited source as having an approved use for multiple sclerosis.

From: Source: European Medicines Agency (EMA), Lemtrada — EPAR, 27/10/2025. © European Medicines Agency. · Data provided by the U.S. Food and Drug Administration. · Source: European Medicines Agency (EMA) — EPAR. © European Medicines Agency.

AI-generated summary of the sources cited on this page, checked automatically against them. Not reviewed by a clinician; not medical advice.

Codes

RxNorm
117055 alemtuzumab
EMA
EMEA/H/C/003718

Official indications

Quoted unchanged from official product information, in English. Listed alphabetically by product, not ranked.

FDA (USA) Campath

1 INDICATIONS AND USAGE CAMPATH is indicated as a single agent for the treatment of B-cell chronic lymphocytic leukemia (B-CLL). CAMPATH is a CD52-directed cytolytic antibody indicated as a single agent for the treatment of B-cell chronic lymphocytic leukemia (B-CLL). ( 1 )

Data provided by the U.S. Food and Drug Administration.

Document date: 20251105 · Official document →

EMA (EU) Lemtrada

Lemtrada is indicated for adult patients with relapsing-remitting multiple sclerosis (RRMS) with active disease defined by clinical or imaging features.

Source: European Medicines Agency (EMA), Lemtrada — EPAR, 27/10/2025. © European Medicines Agency.

Document date: 27/10/2025 · Official document →

Related terms in the cited sources

Has an official indication for

In alphabetical order.

Other treatments A–Z

What people report

Not enough data yet. Anonymous counts appear here only for groups of at least 20 people who agreed to share them.

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External resources

Questions

What is Alemtuzumab approved for in the European Union?

Lemtrada is indicated for adult patients with relapsing-remitting multiple sclerosis (RRMS) with active disease defined by clinical or imaging features. (Source: European Medicines Agency (EMA), Lemtrada — EPAR, 27/10/2025. © European Medicines Agency.)

Sources and attribution

  • Source: European Medicines Agency (EMA) — EPAR. © European Medicines Agency.
  • Data provided by the U.S. Food and Drug Administration.
  • Names other than the official source titles: Anpheros translations and plain-language names, made with AI assistance and checked automatically; the source names are in English.
  • This product uses publicly available data from the U.S. National Library of Medicine (NLM), National Institutes of Health, Department of Health and Human Services; NLM is not responsible for the product and does not endorse or recommend this or any other product.
  • Source: European Medicines Agency (EMA), Lemtrada — EPAR, 27/10/2025. © European Medicines Agency.

Anpheros Search catalog 2026.10.5, published 17 October 2026. About the data →