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BioWorld - Monday, May 18, 2026
Home » Topics » Infection » Coronavirus

Coronavirus
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Other news to note for Feb. 24, 2022

Feb. 24, 2022
Biopharma happenings, including deals and partnerships, grants, preclinical data and other news in brief: Astrazeneca, Atamyo, Conserv, Endpoint, Grifols.
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Regulatory actions for Feb. 24, 2022

Feb. 24, 2022
Regulatory snapshots, including global drug submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Glaxosmithkline, Hightide, Sanofi.
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Mitsubishi, GSK harvest plant-based COVID-19 vaccine win in Canada

Feb. 24, 2022
By Randy Osborne
With the first global approval by Health Canada in hand, Medicago Inc. aims to provide 20 million doses this year of Covifenz – which itself represents another first, as a plant-originated, virus-like particle, recombinant, adjuvanted COVID-19 vaccine. “Hopefully, if all goes well, we’ll be able to do it faster than the last day of the last month” of the year, said Brian Ward, medical officer of Quebec City-based Medicago, a unit of Mitsubishi Tanabe Pharma Corp., which partnered on Covifenz with Glaxosmithkline plc (GSK).
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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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