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GSK Wins U.S. Shingles Vaccine Approval, U.K. Nod for Gene Therapy

Ben Hirschler  |  October 23, 2017

Older adults are most at risk of shingles, a painful, often debilitating blistering rash that results from reactivation of the varicella zoster virus that causes chickenpox and remains latent in those who have had that disease.

Shingrix contains a component from Agenus, which is entitled to royalties on future sales.

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Meanwhile, Britain’s National Institute for Health and Care Excellence (NICE) said on Monday that it had approved GSK’s gene therapy Strimvelis for treating ADA-SCID—better known as “bubble boy” disease—despite its steep price tag of 594,000 euros ($698,000).

Infants with the condition need to be kept in isolation to avoid infections and the cost to the state health service can run to millions of pounds, so a one-off genetic cure can prove cost-effective even at a very high price.

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Filed under:Conditions Tagged with:FDA approvalshinglesShingrixU.S. Food and Drug Administration (FDA)vaccine

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