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BioWorld - Monday, February 9, 2026
Home » Topics » Infection » Coronavirus

Coronavirus
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BioWorld MedTech’s Oncology Extra for Aug. 18, 2020

Aug. 18, 2020
By Mark McCarty and Anette Breindl
Keeping you up to date on recent developments in oncology, including: New and less expensive approach to digital PCR may improve cancer detection; Stromal cell subtypes identified in TNBC; Microbiome metabolites as immunotherapy adjuvants; Pandemic significantly impeded breast cancer follow-up.
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Europe under magnifier/petri dish with coronavirus

Backed by IMI, Europe’s CARE consortium joins COVID-19 fight

Aug. 18, 2020
By Nuala Moran
LONDON – A pan-European consortium backed by 11 pharma companies is pooling resources in a €77.7 million (US$92.5 million) five-year plan to advance development of therapeutics for COVID-19 and other coronaviruses.
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Regulatory front for Aug. 18, 2020

Aug. 18, 2020
The latest global regulatory news, changes and updates affecting biopharma.
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Regulatory actions for Aug. 18, 2020

Aug. 18, 2020
Regulatory snapshots, including global drug submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Astrazeneca, Emmaus, Immatics, Kimera, Krystal.
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In the clinic for Aug. 18, 2020

Aug. 18, 2020
Clinical updates, including trial initiations, enrollment status and data readouts and publications: Acepodia, Aligos, Arrowhead, Clovis, Deciphera, Follicum, GSK, Immatics, Immunicum, Immutep, Intravacc, Maxcyte, Novartis, Organicell, Poseida, Telix, The University of Texas MD Anderson Cancer Center, Ultimovacs, Vanda.
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Digital illustration of U.S., coronavirus

Giroir touts Yale saliva test for COVID-19 as a ‘testing innovation game changer’

Aug. 17, 2020
By Mark McCarty
The COVID-19 pandemic has spurred a considerable amount of testing innovation, including more extensive use of saliva as a medium for detection of pathogens. The U.S. FDA has announced an emergency use authorization (EUA) to Yale School of Public Health for the Salivadirect testing protocol that requires no extraction of the SARS-CoV-2 virus’s RNA, a feature that Assistant Secretary for Health Brett Giroir said is “yet another testing innovation game changer that will reduce demand for scarce testing resources.”
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Rapid testing result for COVID-19

Self-testing from home seen as a valid COVID-19 tracking method

Aug. 17, 2020
By Nuala Moran
LONDON – A large scale population study has shown that home self-testing with low-cost lateral flow diagnostics is a valid way of tracking the COVID-19 pandemic. A total of 105,651 people across the U.K. tested themselves for SARS-CoV-2 antibodies with a fingerprick blood test as part of the REACT (REaltime Assessment of Community Transmission) study.
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Regulatory front for Aug. 17, 2020

Aug. 17, 2020
The latest global regulatory news, changes and updates affecting medical devices and technologies, including: Becton Dickinson, Cartiva, C.R. Bard, Stryker ENT.
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Regulatory actions for Aug. 17, 2020

Aug. 17, 2020
Regulatory snapshots, including global submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Baxter.
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Other news to note for Aug. 17, 2020

Aug. 17, 2020
Med-tech happenings, including deals and partnerships, grants, preclinical data and other news in brief: Angiodynamics, Anthem, Avateramedical, Brain Scientific, Carterra, Endospan, Forwardttc, Genmark Diagnostics, Hengrui Therapeutics, Magle Chemoswed, Microbot Medical, Quest Diagnostics, Sectra, Sirtex Medical, Swift Biosciences, Thermo Fisher Scientific, Tissue Regenix Group, Todos Medica.
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