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BioWorld - Monday, May 11, 2026
Home » Topics » Infection » Coronavirus

Coronavirus
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UK biotech RQ Bio emerges with $157M COVID-19 antibody deal with Astrazeneca

May 17, 2022
By Richard Staines
An unknown U.K. biotech, RQ Biotechnology Ltd., has emerged from stealth mode with a $157 million licensing deal with Astrazeneca plc for its monoclonal antibodies, aimed at protecting vulnerable and immunosuppressed people against SARS-CoV-2.
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Regulatory actions for May 17, 2022

May 17, 2022
Regulatory snapshots, including global submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Exactech, Jointmedica, Labcorp. 
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Regulatory actions for May 17, 2022

May 17, 2022
Regulatory snapshots, including global drug submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Astrazeneca, Atamyo, Eli Lilly, Faron, Galera, Gedeon, Inmagene, Junshi, Mitsubishi, Point, Scpharmaceuticals, Sifi, Travere, Valneva, Zenas.
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Other news to note for May 17, 2022

May 17, 2022
Biopharma happenings, including deals and partnerships, grants, preclinical data and other news in brief: Abeona, Astrazeneca, Benevolentai, Brim, Canbridge, Capsida, Codiak, Coeptis, Cytrx, Kallyope, Kempharm, Mannkind, Nimble, Ora, Orphazyme, Osivax, Poseida, Scholar Rock, Som, Sosei, Surrozen, Ultragenyx, Vivera, Zealand.
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In the clinic for May 17, 2022

May 17, 2022
Clinical updates, including trial initiations, enrollment status and data readouts and publications: Alvotech, Angion, Aruvant, Astrazeneca, Atyr, Avillion, Blade, BMS, Boehringer, Immunicum, Neoleukin, Pharnext, Prota, Puretech, Recordati, Rocket, Synairgen, Urovant.
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GAO sees need for more clarity in FDA enforcement discretion for pandemic tests

May 16, 2022
By Mark McCarty
Among the policies the U.S. FDA’s device center leveraged for testing during the COVID-19 pandemic was the long-standing enforcement discretion lever, which drew less attention than the agency’s use of emergency use authorizations (EUAs). Nonetheless, the Government Accountability Office (GAO) urged the FDA to develop a formal policy for the use of enforcement discretion for pandemic-related tests, including some metrics for when that discretion would come to an end.
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Henley Ion prototype device

Henley Ion reports positive results for viral protection device

May 16, 2022
By Catherine Longworth
Henley Ion LLC has released data showing its filter-less respirator device can remove more than 99% of SARS-CoV-2 bioaerosols. The mask prototype developed by physician and surgeon Julian Henley, uses micronized electrostatic precipitation (mEP) to remove infectious aerosol particles from both inhaled and exhaled air. Results from the study have been published in the Viruses journal and confirm the device can provide equivalent protection from infectious bioaerosols as N95 respirators.
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Europe scraps order for 60M doses of Valneva COVID vaccine

May 16, 2022
By Richard Staines
Valneva SE’s share price plummeted May 16 after the European Commission decided to terminate an advance purchase agreement for millions of doses of its COVID-19 vaccine candidate VLA-2001 because of delays in development. The company’s shares (Paris:VLA) fell more 19% to €9.65 (US$10.07) after it said it would reconsider its financial guidance for 2022.
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Regulatory actions for May 16, 2022

May 16, 2022
Regulatory snapshots, including global drug submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Checkpoint, Clearmind, Editas, Hansa, Mitsubishi Tanabe, Neurocrine, Polarityte, UCB, Yiling.
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In the clinic for May 16, 2022

May 16, 2022
Clinical updates, including trial initiations, enrollment status and data readouts and publications: Affimend, Akston, Altrubio, Astex, C4, Dizal, Hua, Inhibrx, Xeris.
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