Sutimlimab

Therapeutic-first for cold agglutinin disease haemolytic anaemia

21 November 2022 | By Catherine Eckford (European Pharmaceutical Review)

The European Commission has approved Enjaymo®, the first-and-only approved therapeutic for haemolytic anaemia in adults with cold agglutinin disease.

drug products of various forms in various types of packaging, including liquid in glass vials and pills/capsules in blister packages - idea of medicines or pharmaceuticals

news

EMA human medicines committee (CHMP) highlights, September 2022

21 September 2022 | By Hannah Balfour (European Pharmaceutical Review)

In its latest meeting, the Committee for Medicinal Products for Human Use (CHMP) recommended 12 medicines for approval, including those for rare diseases, osteoporosis and cancer.

news

FDA grants priority review to Biologics License Application for sutimlimab

20 May 2020 | By Victoria Rees (European Pharmaceutical Review)

The FDA has granted priority review of the Biologics License Application for sutimlimab to treat haemolysis in patients with cold agglutinin disease (CAD).

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Sutimlimab

Therapeutic-first for cold agglutinin disease haemolytic anaemia

EMA human medicines committee (CHMP) highlights, September 2022

FDA grants priority review to Biologics License Application for sutimlimab