EMA’s PRAC Suggests Restricting Zinbryta in Certain MS Patients

The European Medicines Agency is provisionally restricting the use of the multiple sclerosis medicine Zinbryta (daclizumab) to patients with highly active relapsing disease that has failed to respond to certain other treatment, and to patients with rapidly evolving relapsing disease who cannot be treated with other medicines.
Source: International Pharmaceutical Regulatory Monitor