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BioWorld - Thursday, June 25, 2026
Home » Topics » Infection » Coronavirus

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Regulatory actions for Feb. 23, 2022

Feb. 23, 2022
Regulatory snapshots, including global submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Chromacode, Dyad Medical, Medtronic.
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Government regulator, research scheme getting back to normal in the UK

Feb. 23, 2022
By Mari Serebrov
A sense of normalcy is returning to the U.K., at least from a regulatory perspective. The U.K.’s Medicines and Healthcare Products Regulatory Agency will continue to support COVID-19 clinical trials with ongoing regulatory and scientific input, but all further applications and meeting requests for COVID-19 products will be considered according to usual timelines rather than on an emergency basis, the agency said Feb. 23.
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Coronavirus and antibodies

Sanofi-GSK poised to seek approval for new COVID-19 vaccine

Feb. 23, 2022
By Lee Landenberger
In the quest for regulatory approval for their COVID-19 vaccine, Sanofi SA and Glaxosmithkline plc (GSK) said they plan to submit their phase III and booster efficacy study data showing it induced a significant increase in neutralizing antibodies after a primary series of mRNA or adenovirus vaccines.
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Regulatory actions for Feb. 23, 2022

Feb. 23, 2022
Regulatory snapshots, including global drug submissions and approvals, clinical trial approvals and other regulatory decisions and designations: 4D Pharma, AB Science, Abbvie, Armata, Bharat Biotech, Beigene, Cansino, Homology, Ocugen, Provention, RDIF.
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Other news to note for Feb. 23, 2022

Feb. 23, 2022
Biopharma happenings, including deals and partnerships, grants, preclinical data and other news in brief: Ariana, Atma Journey, Aulos, Cyclerion, Filament, Foresee, Jnana, Synaptogenix, Trpharm and Vicore.
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British pound symbol

Oxdx raises funds for pathogen identification technology

Feb. 22, 2022
By Nuala Moran
LONDON – Oxford University spinout Oxdx Ltd. has raised £2.6 million (US$3.6 million) in pre-seed funding to advance development of a technology for directly identifying infectious pathogens without the need to purify, culture or amplify samples first. The instant testing method uses a mixture of a single universal reagent, high resolution microscopy and machine learning, to identify specific species and strains of bacteria, viruses and other pathogens within minutes.
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Architectural pillars

Cytodyn’s promotion of leronlimab lands it in trouble again

Feb. 22, 2022
By Mari Serebrov
Once again, the U.S. FDA is calling out Cytodyn Inc. for promoting its investigational new drug, leronlimab, as safe and effective against COVID-19.
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Regulatory actions for Feb. 22, 2022

Feb. 22, 2022
Regulatory snapshots, including global submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Abbott, Foundation Medicine, Gramercy Extremity Orthopedics, Lumiradx, Olympus, Precisis.
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Synairgen shares smashed after phase III trial of inhaled COVID therapy fails

Feb. 22, 2022
By Richard Staines
Shares in Synairgen plc have cratered after a phase III trial of its inhaled COVID-19 therapy SNG-001 failed to produce conclusive results, with the company blaming improvements in standard care for the disappointing findings in patients hospitalized with the disease. The Southampton, U.K.-based biotech’s shares (LSE:SNG) touched lows of 10 pence, down 94%, and stabilized around 85% below their previous closing price of £25.36 after the announcement on Monday.
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COVID-19 vaccine and syringe with flag of China

China widens COVID-19 booster choices

Feb. 22, 2022
By Mari Serebrov
China is the latest country mixing things up when it comes to COVID-19 boosters. Since boosters were implemented in China in October, adults have been given a third dose of their primary vaccine regimen, which has consisted of one of three inactivated vaccines produced by Sinopharm Group Co. Ltd. and Sinovac Biotech Ltd.
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