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BioWorld - Tuesday, May 5, 2026
Home » Topics » Infection » Coronavirus

Coronavirus
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Other news to note for Feb. 3, 2022

Feb. 3, 2022
Biopharma happenings, including deals and partnerships, grants, preclinical data and other news in brief: Amylyx, Glaxosmithkline, Johnson & Johnson, Merck, Mitsubishi Tanabe Pharma America, Pfizer, Qilu Regor, Regor, Ridgeback, Vir, Xbiotech.
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Flag of the Russian Federation

Russia preparing for WHO accreditation

Feb. 2, 2022
By Mari Serebrov
Russia’s Ministry of Health is looking to extend its role on the global stage. Over the next few months, the ministry, along with other regulatory agencies in Russia, said it plans to start the accreditation process of coming into compliance with World Health Organization (WHO) standards.
Read More

Crossing boundaries: HDT takes the COVID-19 battle to the world

Feb. 2, 2022
By Lee Landenberger
HDT Bio Corp. looked at the world and saw health care inequity, so it built itself to help countries with developing economies help themselves. The company is bringing RNA technology for handling COVID-19 to underserved areas such as Brazil so they can develop, manufacture and distribute their own vaccine instead of relying on big pharma or developed-nation governments.
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Pandemic lessons fuel reignition of US cancer moonshot

Feb. 2, 2022
By Mari Serebrov
Since COVID-19 hit the U.S. in 2020, the pandemic has taken more than 800,000 American lives. In that same time, cancer has claimed 1.2 million lives, President Joe Biden said Feb. 2 as he “reignited” the cancer moonshot he first launched in 2016 when he was serving as vice president.
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US FDA begins review of vaccine for youngest Americans

Feb. 2, 2022
By Mari Serebrov
Amid pressure to get a COVID-19 vaccine authorized for infants and toddlers sooner than later, Pfizer Inc. and Biontech SE initiated a rolling submission seeking to amend the U.S. FDA’s emergency use authorization for their mRNA vaccine to include children 6 months through 4 years of age.
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Man having temperature check

UK challenge trial lays foundation for accelerated COVID-19 studies

Feb. 2, 2022
By Nuala Moran
LONDON – The first human challenge study of SARS-CoV-2 infection has reported initial results, showing it is safe to infect healthy volunteers with the virus in controlled conditions, and paving the way for the model to be used to accelerate clinical trials of COVID-19 vaccines, antivirals and diagnostics.
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Regulatory actions for Feb. 2, 2022

Feb. 2, 2022
Regulatory snapshots, including global drug submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Azafaros, Brand Institute, Denovo, Immune-Onc, Janssen, Moderna, Mydecine, Ose, Pharmather, Veloxis, Viiv.
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In the clinic for Feb. 2, 2022

Feb. 2, 2022
Clinical updates, including trial initiations, enrollment status and data readouts and publications: Aldeyra, Anavex, Arcutis, Biofrontera, Clarity, Cytokinetics, Immunitybio, Lava, Minerva, Neuvivo, Oncorena, Reviva, Sellas, Trevi, Windtree, Valneva.
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Packaging and kit components

Testing shortage persists in US despite billions spent by federal government

Feb. 1, 2022
By Mark McCarty
The availability of rapid antigen tests for the COVID-19 pandemic has been far short of ideal in recent weeks despite a recent order by the Biden administration for half a billion tests. The question of whether additional federal dollars are forthcoming for additional tests is up in the air, however, due to congressional concerns that there is roughly $800 million in unspent federal dollars, a signal that any additional monies might not be made available any time in the near term.
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Russia preparing for WHO accreditation

Feb. 1, 2022
By Mari Serebrov
Russia’s Ministry of Health is looking to extend its role on the global stage. Over the next few months, the ministry, along with other regulatory agencies in Russia, said it plans to start the accreditation process of coming into compliance with World Health Organization (WHO) standards.
Read More
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