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BioWorld - Wednesday, July 1, 2026
Home » Topics » Infection » Coronavirus

Coronavirus
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Gloved hand holding Veros platform

$65M investment says instrument-free COVID-19 testing makes Sense

Nov. 18, 2021
By Annette Boyle
Sense Biodetection Ltd. closed a $65 million series B investment round on a high note with an additional $15 million pouring in from previous investors. The Abingdon, England-based company raised $50 million in a first tranche of the round in April. Koch Disruptive Technologies LLC, a subsidiary of Koch Industries Inc., led both parts of the round.
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Vials, syringes, pills and masks

Feds show EPIC-PEP for Pfizer’s Paxlovid in COVID-19; gusto garners near-$5.3B contract

Nov. 18, 2021
By Randy Osborne
Pfizer Inc. scored a $5.29 billion deal with the U.S. government to provide 10 million courses of the company’s oral antiviral candidate Paxlovid (PF-07321332; ritonavir) for COVID-19, as Astrazeneca plc and Novavax Inc. also generated news in the space. Paxlovid, if approved or authorized, would be the first oral antiviral of its kind: a 3CL protease inhibitor specifically designed to combat SARS-CoV-2. New York-based Pfizer is seeking emergency use authorization (EUA) from the FDA. Rolling submissions have also commenced in several other countries, and the company continues to build its case for regulatory agencies around the world.
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Regulatory actions for Nov. 18, 2021

Nov. 18, 2021
Regulatory snapshots, including global drug submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Abbvie, Astrazeneca, Biogen, Biohaven, Cytodyn, Eisai, Mirati, Moderna, Novavax, Owp, Pfizer, Prilenia, Santhera, Serum Institute, Zentalis.
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Other news to note for Nov. 18, 2021

Nov. 18, 2021
Biopharma happenings, including deals and partnerships, grants, preclinical data and other news in brief: Abeona, Aglaia, Arcus, Artizan, Biohaven, Clover, Entheotech, Enveric, Eqrx, Filament, Genomma, Gilead, Linus, Mymd, Oramed, Oravax, Owkin, Pierre Fabre, Ribonexus, Sanofi.
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Virus and drug illustration

Roche steps away from COVID-19 development deal with Atea

Nov. 17, 2021
By Lee Landenberger
Roche Holding AG is walking away from a deal with Atea Pharmaceuticals Inc. to co-develop the COVID-19 oral antiviral treatment AT-527 after the mid-October failure of a global phase II study testing the medicine in non-hospitalized adults with mild or moderate disease missed its primary endpoint. Roche’s decision tosses the rights and licenses back to Atea so it can continue its development and commercialization efforts.
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Other news to note for Nov. 17, 2021

Nov. 17, 2021
Biopharma happenings, including deals and partnerships, grants, preclinical data and other news in brief: Abintus, Acceleron, BMS, Bright Peak, Coimmune, Denali, Epivax, GSK, ICER, Imugene, Leidos, Livzon, Merck & Co., Merck KGaA, Mirum, Orange Grove, Pyramid, Pfizer, RDIF, Takeda, Trillium, Vir, Voronoi and Yeda.
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In the clinic for Nov. 17, 2021

Nov. 17, 2021
Clinical updates, including trial initiations, enrollment status and data readouts and publications: Aadi, Aimmune, Amarin, Apnimed, Aobiome, Biohaven, Cellectar, Cend, Codiak, Cytokinetics, Glycomimetics, Hansa, Imara, Inovio, Kezar, Lexicon, Mesoblast, Milestone, Mind Medicine, Moderna, Molecular Partners, Northsea, Oncotelic, Orexo, Ose, Outlook, Phasebio, Pluristem, Puretech, Spruce, Tevogen, Vigeo.
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Health professional holding stethoscope with health icons

Jefferies report: Investor appetite for health care is strong

Nov. 16, 2021
By Catherine Longworth
A research report by global investment bank Jefferies has found increased investor optimism in the health care market amid COVID-19, with respondents expecting stocks to rise throughout 2022. The Jefferies Healthcare Temperature Check summarizes the views of 500 leaders across the health care sector. Sixty percent of respondents said they believed the MSCI World Health Care Index would be higher by the end of 2022 than at present.
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FDA Approved stamp

US approvals slip, delays mount, during busy year for regulatory actions

Nov. 16, 2021
By Karen Carey
A busy regulatory environment globally throughout most of 2021 has translated into more than 15% of all actions taken relating to the COVID-19 pandemic, yet only one product has been approved in the U.S. for the SARS-CoV-2 virus.
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Patient recruitment to stop in Molecular Partners’ COVID-19 phase III study of ensovibep

Nov. 16, 2021
By Lee Landenberger
A futility analysis of Molecular Partners AG’s ensovibep for treating hospitalized COVID-19 adults prompted an independent data safety monitoring board to recommend discontinuing recruitment of patients in the phase III ACTIV-3 study.
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