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BioWorld - Friday, July 10, 2026
Home » Topics » Infection » Coronavirus

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Regulatory front

ICER adjusts Veklury price models – again

Nov. 11, 2020
By Mari Serebrov
The latest global regulatory news, changes and updates affecting biopharma, including: MHRA advises on minimizing trial disruptions.
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Regulatory actions for Nov. 11, 2020

Nov. 11, 2020
Regulatory snapshots, including global drug submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Angiocrine, Bioxcel, Gyroscope, Inventiva, Sebela, Sorrento, Surface.
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Other news to note for Nov. 11, 2020

Nov. 11, 2020
Biopharma happenings, including deals and partnerships, grants, preclinical data and other news in brief: Agenus, Adaptive, Alcresta, Biontech, Biovaxys, Curis, Glaxosmithkline, Hebecell, Immuron Intellia, Myokardia, Nanoviricides, Oncimmune, Origimed, Parexel, PDS, Pfizer, Proteintech, Puretech, Recce, Reven, Revive, Takeda, Tiziana, Vapogenix, Xoma.
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In the clinic for Nov. 11, 2020

Nov. 11, 2020
Clinical updates, including trial initiations, enrollment status and data readouts and publications: AGTC, Ampio, Asieris, Blueberry, Cynata, Deciphera, Edgewise, Five Prime, Gyroscope, Henlius, Lineage, Lumos, Mesoblast, Oncternal, Pfizer, Prilenia, RDIF, Reven, Sagent, Xbrane.
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Illustration of mouths coughing into hands

Quick cough tests reliably ID asymptomatic COVID-19, other conditions

Nov. 10, 2020
By Annette Boyle
As cases skyrocket and more questions arise about the high rate of false negatives returned by rapid testing in COVID-19 cases, a simple, new diagnostic test offers far greater accuracy. Researchers around the globe have found that artificial intelligence can detect coronavirus infections in recorded forced coughs, with nearly 100% accuracy in asymptomatic or presymptomatic cases, making it an ideal quick screening test. Forced cough or voice analysis shows strong results in other conditions, too, including pulmonary hypertension and, surprisingly, Alzheimer's disease.
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Regulatory front

FDA announces class I recall of Stryker Trevo XP

Nov. 10, 2020
By Mark McCarty
The latest global regulatory news, changes and updates affecting medical devices and technologies, including: CDC updates vaccine guidance; Russia launches doctor-driven shortage reporting service.
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Regulatory actions for Nov. 10, 2020

Nov. 10, 2020
Regulatory snapshots, including global submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Biocartis, Icotec, Materialise, Medcad.
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Other news to note for Nov. 10, 2020

Nov. 10, 2020
Med-tech happenings, including deals and partnerships, grants, preclinical data and other news in brief: Anpac Bio-Medical Science, Applied DNA Sciences, Argentum Medical, Ascendum Solutions, Beckman Coulter, Bone Therapeutics, Casetabs, Contakt World Technologies, Dnanudge, Exergen, Foshion Dental, GE Healthcare, Genesiscare, Genosity, GT Medical Technologies, Hologic, Hst Pathways Systems & Technologies, Igentify, Intervenn Biosciences, Iremedy Healthcare Companies, Logicink, Luxcreo, Oxford Immunotec Global, Penumbra, Precision Genetics, Promaxo, Rapid AI, Speedx, Tscan Therapeutics, Wheeler Labs.
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Dollar sign droplet above test tube

R&D investments soar as biopharmas focus on therapies to tackle COVID-19

Nov. 10, 2020
By Peter Winter
According to an analysis conducted by BioWorld of the third-quarter 2020 financial reports filed by public biopharmaceutical companies with market caps greater than $1 billion, and excluding big pharma companies, the amount that was invested in research and development (R&D) during the nine-month period increased by almost 21% compared to the same period last year. The spending was bolstered by companies turning their attention to focus their research on therapies and vaccines to tackle COVID-19.
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Lilly’s COVID-19 antibody has emergency use authorization; who will receive it?

Nov. 10, 2020
By Lee Landenberger
Now that the FDA has granted emergency use authorization to Eli Lilly and Co.’s bamlanivimab, the company plans to manufacture up to 1 million doses of the therapy by year-end with worldwide distribution to mild to moderate COVID-19 patients ages 12 and older in early 2021.
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