( 2 images )<\/span><\/figcaption>CureVac has not publicly determined at which checkpoint it would publish first results but has said it expects to file for European authorization in late May or early June.<\/p>\n
Current infection rates in participating country Peru, in particular, have put CureVac well on track to meet its timetable, Haas said.<\/p>\n
As CureVac\u2019s only major supply deal, the European Union in November last year secured up to 405 million doses of the shot, of which 180 million are optional.<\/p>\n
The Nasdaq-listed firm, which is backed by investor Dietmar Hopp, GlaxoSmithKline as well as the German government, has said it aims to produce up to 300 million doses of the vaccine in 2021 and up to 1 billion in 2022.<\/p>\n
The CEO, which has flagged equipment and material supply issues due to the U.S. Defense Production Act, confirmed the production target, but said that some volumes may not be cleared for delivery before the first quarter of 2022.<\/p>\n
This is due to \u201cvalidation by regulators\u201d that is needed for the release of the produced volumes to customers, which may require additional time, he said.<\/p>\n
For the trial read-out expected later this month, CureVac will publish details on its primary goal of preventing COVID-19 across all virus variants.<\/p>\n
It also aims to disclose efficacy data specifically on the variant known as B117 that was first detected in Britain, as well as on the initial variant that emerged in Chinese city of Wuhan.<\/p>\n
All infections in the trial will undergo genetic sequencing of any variant, offering a unique picture of the variations of the pathogen in Europe and Latin America.<\/p>\n
\u201cWe\u2019ll have the only study that will offer real-world data on the current distribution of variants,\u201d said Sarah Fakih, the firm\u2019s head of investor relations.<\/p>\n
Source: Read Full Article<\/a><\/p>\n","protected":false},"excerpt":{"rendered":"
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