Skip to Main Content
Skip Nav Destination

The requirements to gain licensure and manufacture a vaccine for human use are multifaceted, costly, and time-consuming. Despite the expenditure and challenges, preventative vaccines are considered one of the most cost-effective and efficient means to contain outbreaks and prevent epidemics. In the face of the 2013–2016 Ebolavirus disease (EVD) outbreak, which was the largest EVD outbreak to date and the third Public Health Emergency of International Concern in history, numerous partners from the public and private sectors combined efforts and resources to develop an investigational Zaire ebolavirus (EBOV) vaccine candidate (rVSVΔG–ZEBOV–GP) as quickly as possible. The rVSVΔG–ZEBOV–GP vaccine was approved as ERVEBO™ by the EMA and FDA in late 2019 after five years of clinical development. This chapter describes the development program of this EBOV vaccine.

You do not currently have access to this chapter, but see below options to check access via your institution or sign in to purchase.
Don't already have an account? Register
Close Modal

or Create an Account

Close Modal
Close Modal