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BioWorld - Thursday, March 12, 2026
Home » Topics » Infection » Coronavirus

Coronavirus
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CEO holding Febridx

Lumos Diagnostics nabs $17.9M for rapid POC test

Oct. 7, 2020
By Meg Bryant
Lumos Diagnostics Holdings Pty. Ltd. scooped up AU$25 million (US$17.9 million) in an oversubscribed pre-IPO ahead of its anticipated 2021 listing on the Australian Securities Exchange (ASX). The funds will be used to expand manufacturing operations in California and Florida and to grow the commercial footprint of Febridx, a rapid point-of-care (POC) test that can determine if a person has a viral or bacterial infection within 10 minutes.
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Coronavirus and coins
2020 Medical Innovation Summit

Panelists address challenges related to health care investment in the wake of COVID

Oct. 7, 2020
By Liz Hollis
The ongoing pandemic brought about several challenges for investors looking for the next big thing, but some areas still have experienced growth. Experts addressed this topic and other issues during a panel discussion Tuesday at the Cleveland Clinic’s 2020 Medical Innovation Summit. Moderator Lydia Ramsey Pflanzer, health care editor, Business Insider, highlighted a bright spot, noting that by the end of the third quarter, digital health startups were doing well, raising $9.4 billion, according to Rock Health.
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Surgeon at workstation for surgical robot
Virtual Medtech Conference

The future of robotic-assisted surgery looks bright despite COVID-19

Oct. 7, 2020
By Mary Ellen Schneider
The COVID-19 pandemic has been a bump in the road for developers of digital surgical systems that include robotics, but the technology is still in demand. That was the message from industry leaders at the Advanced Medical Technology Association’s Virtual Medtech Conference.
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Regulatory actions for Oct. 7, 2020

Oct. 7, 2020
Regulatory snapshots, including global submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Hologic.
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Other news to note for Oct. 7, 2020

Oct. 7, 2020
Med-tech happenings, including deals and partnerships, grants, preclinical data and other news in brief: 20/20 Bioresponse, Adm Tronics Unlimited, Ambu, Anpac Bio-Medical Science, Capillary Biomedical, Cb2 Insights, Decipher Biosciences, lectromedical Technologies, Ellume, Evicore Healthcare, Exact Sciences, Exonbio, Imagin Medical, Imed Surgical, Lequest, Lighthouse Imaging, Maverick County Medical, Medicine Discovery Catapult, Integrated Health, Oncimmune, Oncomfort, Origin, Orthex, Orthopediatrics, Paley Orthopedic and Spine Institute, Pfizer, Polarean Imaging, Philips, Qosina, Quanterix, Resolution Medical, Sonic Healthcare, Squadron Capital, Synthace, Todos Medical, Ubiquitome, Vygon.
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In the clinic for Oct. 7, 2020

Oct. 7, 2020
Clinical updates, including trial initiations, enrollment status and data readouts and publications: Medmira, Pulse Biosciences.
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Coronavirus and antibodies

Lilly seeks EUA for COVID-19 antibody treatment

Oct. 7, 2020
By Michael Fitzhugh
With an ongoing phase II trial showing that a pair of its SARS-CoV-2 neutralizing antibodies has so far reduced viral load, symptoms and COVID-19-related hospitalization and ER visits, Eli Lilly and Co. has asked the FDA to consider an emergency use authorization (EUA) for one of the components, LY-CoV555.
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Vaccine guidance, adcom a matter of raising public trust

Oct. 7, 2020
By Mari Serebrov
With COVID-19 cases once again surging across the globe and several countries considering targeted lockdowns, vaccines remain the best hope of restoring a sense of normalcy amidst the pandemic. For vaccines to work though, people must have enough confidence in the efficacy and safety that they’re willing to get vaccinated when the vaccines become available. That’s why the emergency use authorization (EUA) guidance the FDA released Oct. 6 for COVID-19 vaccines is so important.
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U.K. flag on stethoscope

Growing concerns over decline in non-COVID-19 clinical testing, says U.K.’s ABPI

Oct. 7, 2020
By Nuala Moran
LONDON – Industry is calling on the government to set out a plan for the safe and sustainable restart of non-COVID-19 clinical studies that were put on hold when the pandemic struck.
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Regulatory actions for Oct. 7, 2020

Oct. 7, 2020
Regulatory snapshots, including global drug submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Aprea, Arca, Arch, Biomarin, Eton, Lilly, OWP, Pluristem, Polarean, TLC, Y-Mabs.
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