A Phase 3b, Open-label, Multi-country, Multi-centre, Long-term Follow-up Study of ZOSTER-049 (Follow-up of ZOSTER-006/022 Studies) to Assess the Prophylactic Efficacy, Safety and Persistence of Immune Response of a Herpes Zoster Subunit Vaccine and Assessment of Persistence of Immune Response and Safety of 1 or 2 Additional Doses Administered in ZOSTER-049 in 2 Subgroups of Older Adults
Latest Information Update: 24 Jan 2024
At a glance
- Drugs GSK 137173A (Primary)
- Indications Herpes zoster
- Focus Adverse reactions; Registrational
- Acronyms ZOSTER-101
- Sponsors GlaxoSmithKline; GSK
Most Recent Events
- 17 Jan 2024 Planned number of patients changed from 3662 to 3038.
- 17 Jan 2024 Planned End Date changed from 24 Aug 2027 to 23 Aug 2027.
- 17 Jan 2024 Planned primary completion date changed from 23 Jan 2024 to 23 Aug 2027.