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BioWorld - Tuesday, July 28, 2026
Home » Topics » Infection » Coronavirus

Coronavirus
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Other news to note for Nov. 5, 2021

Nov. 5, 2021
Biopharma happenings, including deals and partnerships, grants, preclinical data and other news in brief: Ares, Omeros, Oncopeptides, Resverlogix, Reven Holdings, Spirovant Sciences, Tranquis.
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DNA illustration

Fapon Biotech takes over DNA sequencing firm Sequlite ahead of planned IPO

Nov. 4, 2021
By Doris Yu
Fapon Biotech Inc. expanded its presence in the global next-generation sequencing (NGS) market by acquiring all of the shares in U.S. firm Sequlite Genomics US Inc. With the acquisition, the Dongguan, China-based Fapon Biotech will manage Sequlite’s product development and business operation.
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Molnupiravir capsules

UK authorizes high-profile COVID-19 pill

Nov. 4, 2021
By Michael Fitzhugh
A closely watched oral antiviral for the treatment of mild to moderate COVID-19 will soon be available in Britain after a conditional authorization by the U.K. Medicines and Healthcare products Regulatory Agency. Developed by Ridgeback Biotherapeutics Inc. and Merck & Co. Inc., the drug will be marketed as Lagevrio (molnupiravir) and made available via a national study this winter, the government said.
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Regulatory actions for Nov. 4, 2021

Nov. 4, 2021
Regulatory snapshots, including global drug submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Allena, Astrazeneca, BMS, Biontech, Daiichi, Inovio, Effrx, Enlivex, Epizyme, Innovent, Inovio, Kangtai, Lipocine, Macrogenics, Menarini, Merck, Merus, Minerva, Neurona, Novavax, Ocugen, OS, Pfizer, Rafael, Ridgeback, Transthera, Union, Y-mabs.
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Other news to note for Nov. 4, 2021

Nov. 4, 2021
Biopharma happenings, including deals and partnerships, grants, preclinical data and other news in brief: 2seventy, AC Immune, Affimed, Alterity, Amgen, Aptose, Ardelyx, Astrazeneca, Betterlife, Bluebird, Cassava, Cour, Epivax, Hanmi, Inspirna, Ironwood, Karolinska, Maruho, Omass, Oncternal, Orion, Phagelux, Recode, Soligenix, Tranquis, Umecrine Cognition, Uvax, Vyne, Xoma.
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Regulatory actions for Nov. 3, 2021

Nov. 3, 2021
Regulatory snapshots, including global submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Insightec, Lumos Diagnostics, Mim Software.
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Other news to note for Nov. 3, 2021

Nov. 3, 2021
Med-tech happenings, including deals and partnerships, grants, preclinical data and other news in brief: Aditxt, Betternight, Clario, Cytek Biosciences, Exact Sciences, Heartflow, Innovia, Molex, Nanostring Technologies, Peerbridge Health, Phillips-Medize, Sleep Data Services.
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Covaxin gets nod from WHO as CDC endorses Pfizer’s COVID-19 vaccine for children

Nov. 3, 2021
By Lee Landenberger
A few hours after the U.S. CDC Advisory Committee on Immunization Practices’ Nov. 2 recommendation to allow children ages 5 through 11 to be administered Pfizer Inc. and Biontech SE’s COVID-19 vaccine, Comirnaty (tozinameran), the agency’s director, Rochelle Walensky, endorsed the recommendation. The recommendation came as the World Health Organization (WHO) expanded the COVID-19 vaccines it recommends in the fight against the pandemic by endorsing Bharat Biotech International Ltd.’s Covaxin.
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Financial chart

Biopharma stocks boosted by pandemic, pressured by changing landscape

Nov. 3, 2021
By Karen Carey
Although the BioWorld Biopharmaceutical Index has recovered slightly within the last month, it is showing only a small gain since the start of the year. Up by 2.82%, it is somewhat in line with the Nasdaq Biotechnology Index gain of 4.83%, but significantly beneath the broader markets. The Dow Jones Industrial Average, for example, was up by 17.03% at the end of October.
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Bamlanivimab and etesevimab

Lilly pulls EU filing for COVID-19 antibody cocktail as authorities back rivals, US places $1.29B order

Nov. 3, 2021
By Richard Staines
Eli Lilly and Co. has withdrawn a filing for its COVID-19 antibody cocktail in Europe after health authorities backed rivals – the day after a $1.29 billion purchase of the same medicines from the U.S. government. Indianapolis-based Lilly began filing data from the combination of bamlanivimab and etesevimab in March to enable a fast authorization by the European Medicines Agency.
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