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BioWorld - Saturday, February 14, 2026
Home » Topics » Infection » Coronavirus

Coronavirus
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J&J says its booster is OK

Sep. 21, 2021
By Lee Landenberger
Fresh data from Johnson & Johnson show COVID-19 protection dramatically increased with a booster shot of its single-dose vaccine, adding momentum to the U.S. drive for boosters.
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Australian flag on laptop screen with health professional

TGA provides clarity on software for rapid antigen tests for COVID-19

Sep. 21, 2021
By Mark McCarty
The COVID-19 pandemic is still swirling about, and rapid antigen tests are still playing a vital role in pushing back against the COVID-19 pandemic, and Australia’s TGA has responded with a guidance on when software used with rapid antigen tests qualifies as a regulated device. The TGA has classified such software as a class 3 device when used with a rapid antigen self-test, thus requiring a separate regulatory application before it can be eligible for entry in the Australian Register of Therapeutic Goods (ARTG).
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Regulatory actions for Sept. 21, 2021

Sep. 21, 2021
Regulatory snapshots, including global drug submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Biogen, Biontech, Celltrion, Exelixis, Forge, Incyte, Luye, Marinus, Pfizer, Rhythm, Samsung.
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In the clinic for Sept. 21, 2021

Sep. 21, 2021
Clinical updates, including trial initiations, enrollment status and data readouts and publications: Gemina Labs, Medalliance, Merit Medical, Retina-AI Health.
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Other news to note for Sept. 20, 2021

Sep. 21, 2021
Biopharma happenings, including deals and partnerships, grants, preclinical data and other news in brief: 180, 4C Biomed, Accession, Adaptimmune, Amgen, Appili, Aruvant, Attillaps, Blade, Boehringer Ingelheim, Celltrion, Celularity, Defence, Dyne, Elicio, Evgen, Fujifilm, Galapagos, Glaukos, Immunocore, Intracellular, Mindset, Nanomerics, Novartis, Oncolytics, Oncternal, Oxford, Partner, PTC, Spectrumx, Trigone, Verastem, Virpax.
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Coronavirus and antibodies

FDA clears Memed’s point-of-care infectious disease test

Sep. 20, 2021
By Catherine Longworth
The U.S. FDA has cleared Memed Diagnostics Ltd.'s blood test for distinguishing between bacterial and viral infections. The diagnostic test has been tipped as an essential step in the fight against antimicrobial resistance. While most infectious disease tests look for the pathogen, Memed BV is an advanced host immune response test that measures the levels of immune system proteins and applies proprietary algorithms to generate an immune signature.
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Deals vie for the top with neuro, cancer therapies leading the way

Sep. 20, 2021
By Karen Carey
While 2020 is certainly a hard year to beat, 2021 has so far recorded a respectable amount of biopharma deals and is on track to exceed every other year.
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Jeito extends global reach in oversubscribed $625M venture fund

Sep. 20, 2021
By Nuala Moran
LONDON – There were well-deserved celebrations in Paris on Sept. 20, as Jeito Capital toasted the oversubscribed close of its first fund at €534 million (US$625.5 million). This is claimed as the largest European venture fund dedicated to life sciences, exceeding the original target of €500 million, and with €340 million of the total raised under the constraints of the pandemic from January 2020 onward.
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Other news to note for Sept. 20, 2021

Sep. 20, 2021
Med-tech happenings, including deals and partnerships, grants, preclinical data and other news in brief: Aikido, Attillaps, Bluegrass Vascular, Glaukos, Grail, Kerna, Masvida, Medifocus, N2 Biomedical, Orasure Technologies, Precision Coating, Smartlabs.
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Celltrion wins full approval for COVID-19 treatment in South Korea

Sep. 20, 2021
By Gina Lee
Celltrion Inc. is riding high after receiving full approval for Regkirona (regdanvimab), as a treatment for COVID-19 in South Korea, seven months after the Ministry of Food and Drug Safety (MFDS) granted it conditional marketing approval in February 2021.
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