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BioWorld - Sunday, January 18, 2026
Home » Topics » Infection » Coronavirus

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Microscope and coronavirus illustration

Potential COVID-19 cell therapy treatments in development

July 27, 2020
By Peter Winter
Biopharma companies that are focused on cell therapies have reported promising clinical trial results in their ability to treat acute respiratory distress syndrome (ARDS), a condition that has shown to be a significant contributor to higher mortality in COVID-19 cases.
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Week in review for July 20-24 , 2020: Three COVID-19 vaccines generate T-cell responses

July 27, 2020
By Peter Winter
A quick look back at top stories.
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Regulatory actions for July 27, 2020

July 27, 2020
Regulatory snapshots, including global drug submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Astrazeneca, Beigene, Can-Fite, Carisma, Celltrion, Checkmate, Diffusion, Eton, Generex, Gilead, Kite, Kyowa, Merus, Neoimmunetech, Ocugen, Oculis, Pharmacyte, Scpharmaceuticals, Solid.
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Other news to note for July 27, 2020

July 27, 2020
Biopharma happenings, including deals and partnerships, grants, preclinical data and other news in brief: Amag, Amyris, Anacura Group, Astrazeneca, Axoprotego, Biocomo, Boehringer, Centogene, Cerevel, Cyclica, Clearside, Elevar, Eli Lilly, Emergent, Envisionrx, Farmacore, Heat, Immodulon, LGM, Lynk, Medicinova, Nexgen, Novartis, Oasmia, Onconova, Palatin, PDS, Pfizer, Redhill, Rite Aid, Sandoz, Tanner, Tvardi, Venatorx, Zentalis.
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In the clinic for July 27, 2020

July 27, 2020
Clinical updates, including trial initiations, enrollment status and data readouts and publications: 4D Molecular, Aerie, AI Therapeutics, Amarin, Dalcor, Dare, Destiny, Eyepoint, Immunic, Jcyte, Moderna, NGM, Opthea, Promab, Puma, Rezolute, Rigel, TCR2.
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U.S. FDA headquarters

FDA’s Stenzel says agency ‘very interested’ in fingerstick serology as POC screening test

July 24, 2020
By Mark McCarty
The question of screening for the COVID-19 pandemic continues to absorb the interest of both the U.S. FDA and test developers, and Tim Stenzel, director of the FDA’s Office of In Vitro Diagnostics and Radiological Health (OIR), said in a July 22 webinar that the FDA is “very interested” in a fingerstick test at the point of care for screening purposes, adding that the agency sees any such applications as a priority.
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Device in heart

Edwards exceeds Wall Street expectations in Q2, in spite of COVID-19

July 24, 2020
By Meg Bryant
Edwards Lifesciences Corp. reported better-than-expected results when it released its second quarter earnings late July 23, with revenue down 15% to $924 million, from $1.1 billion in the same period of 2019. The results beat Wall Street consensus of $797.5 million, and reflected an uptick in surgical procedures that had been delayed by the COVID-19 pandemic. The Irvine, Calif.-based company sustained a net loss of $121.9 million, or $0.20 per share, based on generally accepted accounting principles (GAAP), a sharp drop from $242.3 million, or $0.38 per share, in the same quarter last year. However, adjusted earnings looked brighter at $0.34 per share.
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Other news to note for July 24, 2020

July 24, 2020
Med-tech happenings, including deals and partnerships, grants, preclinical data and other news in brief: Aroa Biosurgery, A*Star, Baxter International, Bionano Carequality, Dt Medtech, Genetworx, Genomics, Haemonetics, HintMD, Inlog Holdings France, Joimax, Lifehealthcare, Medalliance, Microgendx, Mp Biomedicals, Progenity, Redox, Revance, Synchron, Vilex, Vipun Medical.
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In the clinic for July 24, 2020

July 24, 2020
Clinical updates, including trial initiations, enrollment status and data readouts and publications: enscript, Polarityte.
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BioWorld MedTech’s Neurology Extra for July 24, 2020

July 24, 2020
By Andrea Applegate
Keeping you up to date on recent developments in neurology, including: Novel drug delivery particles use neurotransmitters as a 'passport' into the brain; SARS-CoV-2 infection of non-neuronal cells, not neurons, may drive loss of smell in patients with COVID-19; Pandemic to accelerate adoption of electronic patient portal for epilepsy.
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