Global Statistics

All countries
548,935,393
Confirmed
Updated on June 26, 2022 8:18 pm
All countries
520,730,887
Recovered
Updated on June 26, 2022 8:18 pm
All countries
6,350,765
Deaths
Updated on June 26, 2022 8:18 pm
Tuesday, February 7, 2023

Global Statistics

All countries
548,935,393
Confirmed
Updated on June 26, 2022 8:18 pm
All countries
520,730,887
Recovered
Updated on June 26, 2022 8:18 pm
All countries
6,350,765
Deaths
Updated on June 26, 2022 8:18 pm
Molderizer and Safe Shield

FDA emails show how vaccine leader questioned ‘hyper-accelerated’ 2021 review of Pfizer shot – Endpoints News

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..COVID-19 upsurge in China poses worldwide threat – Office of Communications and Marketing

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FDA Roundup: February 7, 2023 – PR Newswire

FDA Roundup: February 7, 2023  PR Newswire Source link


Less than a week after Eisai and Biogen won accelerated approval from the FDA for their Alzheimer’s drug lecanemab, Executive Editor Drew Armstrong spoke one-on-one with Eisai’s US CEO Ivan Cheung, who also leads the company’s Alzheimer’s efforts. This transcript has been edited for brevity and clarity.

Drew Armstrong:

Welcome everybody. I am Drew Armstrong, the executive editor over at Endpoints News, and I’m exceptionally pleased to be joined by Ivan Cheung from Eisai. He runs the US business and oversees the Alzheimer’s program there. Obviously, you all have had some enormous news in the last week with the accelerated approval of Lecanemab, and congratulations on that. It’s obviously a huge moment for the field, huge moment for your company. I want to jump right in because we have 30 minutes and so much to cover. I’m incredibly excited to get this chance to talk to you. Now, that I’m in San Francisco, you’re in New Jersey. I’m sorry we aren’t able to be together in person, but tons of news from you all. You’ve gotten this accelerated approval.

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