<?xml version="1.0" encoding="UTF-8"?><rss version="2.0"
    xmlns:content="http://purl.org/rss/1.0/modules/content/"
    xmlns:dc="http://purl.org/dc/elements/1.1/"
    xmlns:atom="http://www.w3.org/2005/Atom"
    xmlns:sy="http://purl.org/rss/1.0/modules/syndication/"
    xmlns:media="http://search.yahoo.com/mrss/">
<channel>
    
        <item>
            <title>Moderna says vaccine 100% effective against severe Covid - The Daily Guardian</title>
            <link>https://latest.thedailyguardian.com/others/moderna-says-vaccine-100-effective-against-severe-covid/</link>
            <guid>https://latest.thedailyguardian.com/others/moderna-says-vaccine-100-effective-against-severe-covid/</guid>
            <pubDate>December 1, 2020, 7:04 am</pubDate>
            <description><![CDATA[US biotech company Moderna will apply for US and European emergency authorisation for its Covid-19 vaccine on Monday after full results from a late-stage study showed it was 94.1% effective with no serious safety concerns, the company said. It also said that its vaccine candidate had 100 per cent efficacy against severe disease. According to [&hellip;]
]]></description>
            <content:encoded><![CDATA[
<p>US biotech company Moderna will apply for US and European emergency authorisation for its Covid-19 vaccine on Monday after full results from a late-stage study showed it was 94.1% effective with no serious safety concerns, the company said. It also said that its vaccine candidate had 100 per cent efficacy against severe disease.</p>



<p>According to an official statement by the company, the primary efficacy analysis of the “Phase 3 study of mRNA-1273 conducted on 196 cases confirms the high efficacy observed at the first interim analysis. The data analysis indicates a vaccine efficacy of 94.1 per cent. Safety data continue to accrue and the study continues to be monitored by an independent, NIH-appointed Data Safety Monitoring Board (DSMB).”</p>



<p>Moderna said the 196 CCovid-19 cases in its trial included 33 adults over 65 years old and 42 volunteers from racially diverse groups, including 29 Latinos, 6 Blacks, 4 Asian Americans and 3 multiracial participants. There was one death related to Covid-19 in the placebo group.</p>



<p>Moderna plans to request an Emergency Use Authorization (EUA) from the US Food and Drug Administration (FDA) and conditional approval from the European Medicines Agency (EMA).</p>



<p>The Phase 3 study, known as the COVE study, enrolled more than 30,000 participants in the US and is being conducted in collaboration with the National Institute of Allergy</p>
]]></content:encoded>
            <media:content url="https://latest.thedailyguardian.com/wp-content/uploads/2020/11/Moderna.jpg" type="image/jpeg" width="1200" height="675"/>
            <dc:creator>Correspondent</dc:creator>
            <category>newsx</category>
        </item>
</channel>
</rss>