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BioWorld - Thursday, May 21, 2026
Home » Topics » Infection » Coronavirus

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Australian flag on laptop screen with health professional

Australia’s TGA delays overhaul of medical device regulations due to COVID-19

June 22, 2020
By Tamra Sami
PERTH, Australia – Australia’s Therapeutic Goods Administration (TGA) is pushing back implementation dates for numerous medical device reforms due to delays caused by the COVID-19 pandemic.
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Coronavirus microscopic model

Evelo Bio's anti-inflammatory to be tested in hospitalized COVID-19 patients

June 22, 2020
By Michael Fitzhugh
A new U.K. trial evaluating drugs for hospitalized patients in the early stages of COVID-19 has elected to test Evelo Biosciences Inc.'s anti-inflammatory monoclonal microbial, EDP-1815, after an earlier trial found it led to favorable anti-inflammatory activity in psoriasis patients.
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Regulatory actions for June 22, 2020

June 22, 2020
Regulatory snapshots, including global submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Conformis, Mainstay Medical, Medtronic, Omnipathology.
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Other news to note for June 22, 2020

June 22, 2020
Med-tech happenings, including deals and partnerships, grants, preclinical data and other news in brief: Agena Bioscience, Avita, Astrazeneca, Caprion-Histogenex, Clinical Logistics, Gendius, Lantheus, Mevion, Microdermics, Natera, National Jewish Health, Novateur Ventures, Nuprobe, Orfit, Progenics, Qualtrics, Thermo Fisher Scientific, Weigao Group.
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India’s Glenmark Pharmaceuticals gets green light to launch $1 COVID-19 treatment tablets

June 22, 2020
By David Ho
HONG KONG - Mumbai-based Glenmark Pharmaceuticals Ltd. has been granted manufacturing and marketing approval for the launch of its antiviral drug, favipiravir, for the treatment of mild to moderate COVID-19, a move it deems a “landmark development for COVID-19 patients in India.”
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Week in review for June 15-19, 2020: CNS disease-focused companies adjusting clinical programs

June 22, 2020
By Peter Winter
A quick look back at top stories.
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Nabriva's Contepo NDA derailed by COVID-19

June 22, 2020
By Michael Fitzhugh
A second attempt by Nabriva Therapeutics plc to win U.S. approval for the antibiotic Contepo (fosfomycin) has been undone by COVID-19. Manufacturing issues stymied the original NDA. This time, restrictions of FDA staff travel to Europe sunk the venture, leading to a new complete response letter (CRL) for the candidate as a potential treatment of complicated urinary tract infections (cUTI), including acute pyelonephritis.
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Other news to note for June 22, 2020

June 22, 2020
Biopharma happenings, including deals and partnerships, grants, preclinical data and other news in brief: Agenus, Applied Genetic Technologies, Allogene, Amicrobe, Betta, CARB-X, Codiak, Drishti Discoveries, Enhanc3D Genomics, G1, Genor, Halozyme, Immunoprecise, Intravacc, Janssen, La Jolla, Lantheus, Leidos, Litevax, Melinta, Merck, Minerva, Nervgen, Orgenesis, PDS, Precigen, Progenics, Sarepta, Semarion, Spirea, Tetraphase.
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In the clinic for June 22, 2020

June 22, 2020
Clinical updates, including trial initiations, enrollment status and data readouts and publications: Arcutis, Aridis, Aurinia, Evelo, FSD, Heat, Hookipa, Janssen, Merck, Myokardia, Onconova, Pfizer, Revolution, Springworks, Tarsius, Ziopharm.
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Regulatory front for June 22, 2020

June 22, 2020
The latest global regulatory news, changes and updates affecting biopharma, including: Auromedics and Somerset.
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