Drug

Varicella zoster virus envelope glycoprotein e

As of the edition of 20 October 2026, Varicella zoster virus envelope glycoprotein e is a vaccine component: marketed, first approved in 2017 (US); US protection ends in 2029.

Sources: FDA Orange Book and Purple Book, other approval registers, ClinicalTrials.gov, ChEMBL.

The drug

Status
Marketed; latest approval 2017
Kind
Vaccine component
Brand name
Shingrix
First approved
20 October 2017 (US)
Approvals on record
3 in 1 region
Holder of the most recent approval
GSK
Registered trials
51, 2 stopped early
Disease areas
Infections; Immune system; Nervous system; Skin and connective tissue; Blood and lymph; Cancer

US protection

US protection ends in 2029.

US protection ends in 2029, computed as 12 years from the first US licence because FDA publishes no date for this product. The application that gives this date is held by GSK. The date is computed, not published.

This is the US only, and it is not the date generics or biosimilars can enter.

The exact date and the listings behind it

In the product

1 listing counts towards this date. The exact date and each listing are in the product.

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Registered trials

PhaseTrialsCompletedActiveStopped early
Phase not stated2011
Phase 15310
Phase 210640
Phase 3232110
Phase 411091
All trials51

Who ran its trials

CompanyRoleYears
GSKLead sponsor of trials2007 to now