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BioWorld - Thursday, March 23, 2023
Home » Topics » Infection » Coronavirus

Coronavirus
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Shionogi advances oral COVID-19 antiviral ensitrelvir to phase III

Feb. 16, 2023
By Tamra Sami
No Comments
After gaining emergency regulatory approval in Japan for its oral COVID-19 antiviral, 3CL protease inhibitor Xocova (ensitrelvir/S-217622), Shionogi & Co. Ltd. is advancing several global phase III trials across a wide range of COVID-19 patient populations. Branded as Xocova in Japan, ensitrelvir received emergency regulatory approval from Japan’s Ministry of Health, Labour and Welfare in late November 2022 for SARS-CoV-2 infection based on the results from phase II/III trials in non-hospitalized patients in Asia.
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Regulatory actions for Feb. 15, 2023

Feb. 15, 2023
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Regulatory snapshots, including global drug submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Albireo, Athersys, Avidity, Biocon, Healios, Lemonex, Mirum, Neurona, Soligenix, Verve, Viatris.
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Infection

Thylacine licenses exclusive rights to antiviral peptide platform developed at Columbia University

Feb. 15, 2023
No Comments
Thylacine Biotherapeutics Inc. has entered into a license agreement with Columbia University for worldwide exclusive rights to develop and commercialize a novel antiviral peptide platform invented and refined at Columbia.
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In the clinic for Feb. 14, 2023

Feb. 14, 2023
No Comments
Clinical updates, including trial initiations, enrollment status and data readouts and publications: Acer, Acumen, Akari, Alligator, BMS, Boan, Clene, Dermavant, Ena, Frequency, G1, Gensight, IMV, Luye, Moleculin, Ocular, Recbio, Regenxbio, Scancell, Seelos, Silver Creek, Skye.
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Coronavirus and antibodies
Infection

Tonix exercises option to license anti-SARS-CoV-2 monoclonal antibodies from Columbia University

Feb. 14, 2023
No Comments
Tonix Pharmaceuticals Holding Corp. has exercised an option to obtain an exclusive license from Columbia University for the development of a portfolio of fully human (TNX-3600) and murine (TNX-4100) monoclonal antibodies for the treatment or prophylaxis of SARS-CoV-2 infection.
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Illustration of coronavirus blocked by the no symbol
Infection

Novel receptor stymies SARS-CoV-2, study shows

Feb. 14, 2023
By Tamra Sami
No Comments
Scientists at the University of Sydney have discovered a protein in the lung that blocks SARS-CoV-2 infection and forms a natural protective barrier in the human body. Leucine-rich repeat-containing protein 15 (LRRC15) is an inbuilt receptor that binds the SARS-CoV-2 virus without passing on the infection. The discovery opens a new area of immunology research around LRRC15 and suggests a pathway to develop new drugs to prevent viral infection from coronaviruses like COVID-19, but also to deal with fibrosis in the lungs.
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Regulatory actions for Feb. 10, 2023

Feb. 10, 2023
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Regulatory snapshots, including global drug submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Alvotech, Bellerophon, Medicinova, Mesoblast, Regeneron.
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In the clinic for Feb. 10, 2023

Feb. 10, 2023
No Comments
Clinical updates, including trial initiations, enrollment status and data readouts and publications: Artios, Awkn, Biomedical Research & Bio-Products, Cara, Celyad, Cognition, Eiger, Galapagos, Immvira, Kite, Kura, Nexcella, Redx..
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Other news to note for Feb. 10, 2023

Feb. 10, 2023
No Comments
Additional early-stage research and drug discovery news in brief, from: PDS Biotechnology, Tonix Pharmaceuticals.
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Patient receiving shot

Despite strong data, Eiger’s COVID-19 treatment remains blocked

Feb. 9, 2023
By Lee Landenberger
No Comments
Strong data for pegylated interferon lambda, Eiger Biopharmaceuticals Inc.’s experimental COVID-19 treatment, boosted the company stock (NASDAQ:EIGR) 23% on Feb. 9 as the company continues to seek regulatory approval. That approval path is blocked as interferon lambda is not currently approved by the U.S. FDA for any use. In October, the company said it would not submit emergency authorization use request after feedback from the FDA.
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