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BioWorld - Monday, April 13, 2026
Home » Topics » Infection » Coronavirus

Coronavirus
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Colorized transmission electron micrograph of SARS-CoV-2.
Infection

Preclinical data show potential of Maxwell Biosciences' Claromers for SARS-CoV-2

Sep. 30, 2022
Maxwell Biosciences Inc. has announced data on the utility of its Claromer drug discovery platform for the treatment and prevention of SARS-CoV-2, and potentially other respiratory viruses, through a series of preclinical in vitro and in vivo studies.
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Lasker awards 2022

Laskers go for integrins, prenatal testing, COVID-19 dashboard

Sep. 29, 2022
By Anette Breindl
The 2022 Albert Lasker Basic Medical Research Award has been awarded to Richard Hynes, of the Massachusetts Institute of Technology, Erkki Ruoslahti, of the Sanford Burnham Prebys Medical Discovery Institute, and Timothy Springer, of Harvard Medical School “for discoveries concerning the integrins, key mediators of cell-matrix and cell-cell adhesion in physiology and disease.”
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In the clinic for Sept. 29, 2022

Sep. 29, 2022
Clinical updates, including trial initiations, enrollment status and data readouts and publications: Altimmune, Alumis, CNS, Eisai, Evommune, SAB, Shanghai Henlius, Shionogi, Sparrow.
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Other news to note for Sept. 28, 2022

Sep. 28, 2022
Biopharma happenings, including deals and partnerships, grants, preclinical data and other news in brief: Arsenal, Aquestive, Biolinerx, Chimerix, Cognition, Contera, Eagle, Eclipse, Emergent, Enalare, Hitgen, Idorsia, Kbio, Leaf, Maxcyte, Mindset, Ocrugen, Pharmanovia, Pinetree, Resverlogix, Vertex, Visus, Viewpoint.
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In the clinic for Sept. 28, 2022

Sep. 28, 2022
Clinical updates, including trial initiations, enrollment status and data readouts and publications: Achieve, Acticor, Aquestive, Atyr, Aura, Bergenbio, Bio-Thera, Cinrx, Cornerstone, Equillium, Harbour, Ichnos, Kempharm, Medicenna, Modus, Neurosense, Neurophth, Nykode, Ocular, Odyssey, Oncternal, Pepgen, Rallybio, Synthetic Biologics, TCR2, Telix, X4.
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FDA tightens eligibility for COVID-19 emergency use authorization program

Sep. 27, 2022
By Mark McCarty
The COVID-19 pandemic may or may not be over, depending on which member of the U.S. government’s executive branch one asks, but the FDA’s device center has drawn much tighter lines around its emergency use authorization (EUA) program for COVID-19 tests.
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Regulatory actions for Sept. 27, 2022

Sep. 27, 2022
Regulatory snapshots, including global drug submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Aqualung, Atea, Catalym, Everest, Pfizer, Y-mabs.
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Other news to note for Sept. 27, 2022

Sep. 27, 2022
Biopharma happenings, including deals and partnerships, grants, preclinical data and other news in brief: AC Immune, Amerisourcebergen, Celsion, Cytrx, Lipocine, Navigo, Novavax, Outlook, Sciwind, Seagen, Synerk, Zai.
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Valneva vaccine vials

Talks with partner over next-gen COVID-19 shot may take months and could fail, Valneva warns

Sep. 26, 2022
By Richard Staines
Valneva SE is approaching a crucial point with its troubled efforts to develop a COVID-19 vaccine, having announced Sept. 26 it’s in talks with a potential partner for its next-generation jab. The company cautioned the negotiations could take several months and may not succeed. The company’s problems with its COVID-19 vaccine, which is based on an inactivated whole virus, have weighed on its shares (Paris:VLA), which collapsed from a 52-week high of more than €29 (US$28.29) in December 2021 to €5.74 at the close of trading Sept. 26.
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Regulatory actions for Sept. 26, 2022

Sep. 26, 2022
Regulatory snapshots, including global drug submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Amniotics, Avenue, Bausch + Lomb, Biontech, Ferring, Glenmark, Infant Bacterial, Oncopeptides, Pfizer, Rebiotix, Spectrum.
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