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BioWorld - Wednesday, May 13, 2026
Home » Topics » Infection » Coronavirus

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Regulatory actions for April 14, 2022

April 14, 2022
Regulatory snapshots, including global submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Fosun Diagnostics.
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Valneva vaccine vials

Dumped by UK government, Valneva turns to Scotland as regulator approves COVID-19 shot

April 14, 2022
By Richard Staines
The U.K.’s drugs regulator has approved the COVID-19 vaccine from Valneva SE – although the shot is likely only to be offered to health workers in Scotland after the Westminster government rejected it because rivals beat it to market.
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Regulatory actions for April 14, 2022

April 14, 2022
Regulatory snapshots, including global drug submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Affamed, Atyr, Biogen, Boehringer, Briacell, Direct, Eli Lilly, Novavax, Recbio.
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Other news to note for April 14, 2022

April 14, 2022

Biopharma happenings, including deals and partnerships, grants, preclinical data and other news in brief: Biontech, Dyadic, Epygen, Emergex, Excellthera, Hookipa, Inotrem, Insilico, Gain, Geneuro, ICER, Longeveron, Magenta, Matinas, Micros, Oncolytics.


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In the clinic for April 14, 2022

April 14, 2022
Clinical updates, including trial initiations, enrollment status and data readouts and publications: Adiso, Addex, Amryt, Imcyse, Lineage, Medicinova, Oncternal, Phosplatin, Recce, Sonnet, Syneurx, Turning Point.
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COVID-19 vaccine vials

Big pharma CEOs lambast IP waiver and worry over US funding for COVID meds

April 13, 2022
By Richard Staines
Pharma CEOs have pushed back strongly against intellectual property (IP) waivers for COVID-19 vaccines and therapies, saying that pricing is not the reason why middle- and low-income countries have not received pharmaceutical countermeasures against the pandemic. Senior execs from Pfizer Inc., Eli Lilly and Co., and Roche Holding AG, also expressed concerns about the latest funding package from the U.S. government, which at $10 billion is less than half that originally requested by the White House.
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Shionogi’s COVID treatment could disturb fetal development, impact regulatory approval

April 13, 2022
By Gina Lee
Shionogi & Co. Ltd.’s plan to make ensitrelvir, an oral antiviral for COVID-19, the first domestically approved COVID-19 treatment has hit a snag. Animal studies showed the drug, also known as S-217622, disturbed fetal development, according to media reports.
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In the clinic for April 13, 2022

April 13, 2022
Clinical updates, including trial initiations, enrollment status and data readouts and publications: Mallinckrodt, Natera.
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Regulatory actions for April 13, 2022

April 13, 2022
Regulatory snapshots, including global drug submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Aeglea, Affamed, Bharat Biotech, Biocardia, Blue Earth, Fera, Gilead, Henlius, Medilink, Myovant, Ocugen, Paradigm, Poxel, Secura, Vistagen, Xortx.
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Other news to note for April 13, 2022

April 13, 2022

Biopharma happenings, including deals and partnerships, grants, preclinical data and other news in brief: Abbvie, Affyxell, Appili, Applied, Artelo, Artiva, Ascletis, Autigen, Avacta, Bioasis, Biomice,  Blumentech, Boehringer, Captor, China Meheco, Coeptis, Cybin Daewoong, Cyclacel, Cytodyn, Edigne, Janssen, Lysogene, Mallinckrodt, Merck & Co., Mymd, Neuropathix, Oncternal, Oxford, Proqr, Spikimm, Statera, Terran, Yeda.


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