Liver Safety Issues Lead The EMA To Restrict Biogen's MS Drug

The European Medicines Agency restricts the use of Biogen’s MS medication Zinbryta until the completion of a liver safety investigation.

The EMA will allow the treatment for those with highly active relapsing MS who aren’t responding to other treatments or those with rapidly evolving relapsing MS that aren’t eligible for other treatments.

Patients with liver injuries should not receive Zinbryta, and those with autoimmune diseases apart from MS should express caution when considering the drug.

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