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Britain Approves Emergency Use of Pfizer’s COVID Vaccine

The Pharma Data

2, 2020 – Britain became the first Western country to allow emergency use of a coronavirus vaccine on Wednesday, after approving Pfizer’s candidate in the race to inoculate millions of people around the globe. But there are daunting obstacles to the vaccine’s delivery to the masses. WEDNESDAY, Dec.

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COVID Hospitalizations in U.S. Hit Record High

The Pharma Data

As health officials brace for still another surge in cases following Thanksgiving gatherings across the country, some Americans returning from the holiday break faced strict new coronavirus containment measures on Monday, the Associated Press reported. ” Moderna to request emergency approval for its vaccine. .”

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Emotional empathy is driving brand equity

pharmaphorum

million to small businesses to support the Local Initiatives Support Corporation and has offered special prices for nurses and teachers. To take one local example, in the UK Pfizer is working with the National Schools Partnership to make its Superbugs and Vaccines education program suitable for home learning. Verizon also donated $2.5

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Pfizer Responds to Research Claims

Pfizer

In the ongoing development of the Pfizer-BioNTech COVID-19 vaccine, Pfizer has not conducted gain of function or directed evolution research. This research provides a way for us to rapidly assess the ability of an existing vaccine to induce antibodies that neutralize a newly identified variant of concern.

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Clinical Catch-Up: January 18-22 | BioSpace

The Pharma Data

Gritstone Oncology , based in Emeryville, California, announced that it is advancing development of its own second-generation vaccine against COVID-19. It inked a deal with the National Institute of Allergy and Infectious Diseases (NIAID) to launch a Phase I trial. COVID-19-Related. The drug was licensed from Immutep Limited.

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New Data Show Treatment with Lilly’s Neutralizing Antibodies Bamlanivimab (LY-CoV555) and Etesevimab (LY-CoV016) Together Reduced Risk of COVID-19 Hospitalizations and Death by 70 Percent

The Pharma Data

Lilly has received feedback from front-line nurses and doctors administering these infusions regarding the complexity and time requirements for preparation and administration. It remains under review by the FDA. It was identified from a blood sample taken from one of the first U.S. patients who recovered from COVID-19. . www.lilly.com?and?www.lilly.com/news.?P-LLY.

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COVID Daily Death Toll Sets New U.S. Record, Soars Past 4,400

The Pharma Data

health officials have about containing the coronavirus in the coming months, U.S. Health Secretary Alex Azar said Tuesday that the federal government would now release all available vaccine doses and told states to vaccinate every American aged 65 and older. COVID vaccine recommended for all Americans over 65.