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BioWorld - Sunday, March 22, 2026
Home » Topics » Infection » Coronavirus

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Other news to note for Sept. 1, 2022

Sep. 1, 2022
Med-tech happenings, including deals and partnerships, grants, preclinical data and other news in brief: Alnylam, Bio-Techne, Cerveau, Fluidx, Openeye, Pharmajet, Sense Biodetection, Tecomedical.
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Other news to note for Sept. 1, 2022

Sep. 1, 2022
Biopharma happenings, including deals and partnerships, grants, preclinical data and other news in brief: Arcturus, Finch, Liquidia.
Read More

In the clinic for Sept. 1, 2022

Sep. 1, 2022
Clinical updates, including trial initiations, enrollment status and data readouts and publications: Amgen, Biocardia, Bright Minds, Futura, Hepion, Hightide, Hillevax, Immunogen, Lannett, Madrigal, Recordati, Regenxbio.
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Illustration of COVID-19 virus cells affecting brain

FDA warning to COVID test maker suggests no quality system was in place

Aug. 31, 2022
By Mark McCarty
The COVID-19 pandemic encouraged a lot of things, including shoddy product quality, but a recent FDA warning letter suggests that the associated need for tests also encouraged a few operations that had less than a full commitment to quality management. 
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Regulatory actions for Aug. 31, 2022

Aug. 31, 2022
Regulatory snapshots, including global drug submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Astrazeneca, Bavarian Nordic, Biocytogen, Biogen, Curis, Daiichi, Jaguar, Moderna, Novavax, Okyo, Outlook, Sanofi, Sobi, Stemcyte, Takeda, Y-mabs.
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Other news to note for Aug. 31, 2022

Aug. 31, 2022
Biopharma happenings, including deals and partnerships, grants, preclinical data and other news in brief: Codiak, Marinus, Myovant, Pfizer.
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In the clinic for Aug. 31, 2022

Aug. 31, 2022
Clinical updates, including trial initiations, enrollment status and data readouts and publications: Aim, Aristea, Clover, Connect, Cybin, Forge, Hemostemix, Janssen, Jounce, Journey, Poxel, Sangamo, Vascular.
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Vaccine administration

Bivalent COVID-19 boosters coming to the US next week

Aug. 31, 2022
By Mari Serebrov
Right on cue, the U.S. FDA authorized bivalent COVID-19 vaccines from Moderna Inc. and Pfizer Inc.-Biontech SE to be given as boosters at least two months following a primary vaccine series or a previous booster. “These updated boosters present us with an opportunity to get ahead of the next wave of COVID-19,” FDA Commissioner Robert Califf said, following the Aug. 31 announcement.
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Chinese flag and pills

Hansoh acquires global rights to oral antiviral for COVID-19

Aug. 30, 2022
By Doris Yu
Hansoh Healthtech Co. Ltd., part of Jiangsu Hansoh Pharmaceutical Group Co. Ltd., has acquired exclusive worldwide rights to develop and commercialize an oral SARS-CoV-2 3C-like protease inhibitor from Beijing Huayi Health Drug Discovery Institute, also known as the Global Health Drug Discovery Institute (GHDDI). The deal includes ¥12 million (US$1.8 million) up front and up to ¥1.68 billion in potential milestone payments, plus tiered royalties on net sales.
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Regulatory actions for Aug. 30, 2022

Aug. 30, 2022
Regulatory snapshots, including global drug submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Bluebird, Innovent, Moderna, Pfizer, Pharmazz, Plus, Polpharma, Tracon.
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