A second approval for Shingrix, now in the world's largest market

21 October 2017

Late Friday, the US Food and Drug Administration approved Shingrix (zoster vaccine recombinant, adjuvanted) for the prevention of shingles (herpes zoster) in adults aged 50 years and older.

Shingrix, from UK pharma major GlaxoSmithKline (LSE: GSK), is a non-live, recombinant subunit vaccine given intramuscularly in two doses.

The approval was widely expected as just a month ago the FDA’s Vaccines and Related Biological Products Advisory Committee (VRBPAC) voted unanimously that the data support the efficacy and safety of Shingrix for the prevention of herpes zoster or shingles in adults ages 50 and over.

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