UPDATE: On July 19, 2013, Biogen Idec announced that the United States Food and Drug Administration (FDA) had accepted their application for the marketing approval of Plegridy™ in the United States. The FDA will review the drug under its standard review timeline. The European Medicines Agency (an agency in Europe similar to the FDA in the United States) is also reviewing an application for the approval of Plegridy in the European Union.
On May 21, 2013, Biogen Idec submitted a new treatment for multiple sclerosis (MS) to the United States Food and Drug Administration (FDA) for approval. This potential new disease-modifying therapy (DMT) for the long-term treatment of MS is a pegylated version of interferon beta-1a. Using the brand name of “Plegridy™,” if approved, this new product would require fewer injections than the other presently approved self-injectable DMTs for MS.
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