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BioWorld - Wednesday, May 27, 2026
Home » Topics » Infection » Coronavirus

Coronavirus
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Syringe, bottles of COVID-19 vaccine on U.K. map

U.K. launches mixed COVID-19 vaccine trial

Feb. 4, 2021
By Nuala Moran
LONDON – The U.K has started the world’s first trial alternating an adenoviral vectored COVID-19 vaccine with one that delivers the virus spike protein instructions encoded in messenger RNA. The heterologous prime boost trial will recruit 820 participants into an eight-arm study comparing different combinations of the Astrazeneca plc/Oxford University and Pfizer Inc./Biontech SE vaccines, administered in a different order and at different intervals.
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Regulatory actions for Feb. 4, 2021

Feb. 4, 2021
Regulatory snapshots, including global drug submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Astellas, Astrazeneca, EMD, Intrommune, Karyopharm, Sinovac, Theratechnologies.
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Other news to note for Feb. 4, 2021

Feb. 4, 2021
Biopharma happenings, including deals and partnerships, grants, preclinical data and other news in brief: Active, Angelini, Angiotensin, Arvelle, Astrazeneca, Beximco, BMS, BNC, Connectyx, Diamond, Evotec, Famar, Gensight, Golden, Molecular Partners, Neogenomics, Novartis, Novavax, Serum Institute, Sio, Sunshine, Wuxi.
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In the clinic for Feb. 4, 2021

Feb. 4, 2021
Clinical updates, including trial initiations, enrollment status and data readouts and publications: ADC, Agenus, Aldeyra, Aligos, Atea, Biogen, Botanix, Calliditas, Codiak, Corvus, Crinetics, Curevac, Dynavax, Eucure, Gilead, Golden, I-Mab, Innocare, Neurorx, Reistone, Surface Ophthalmology.
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Regulatory front

Industry: Stop Trump’s Part D changes

Feb. 4, 2021
By Mari Serebrov
The latest global regulatory news, changes and updates affecting biopharma, including: FDA weighing Xeljanz safety results; EMA initiates OPEN collaboration; NICE evaluating guidance processes; TGA seeking comments; USPTO extends program with Japan’s, Korea’s patent offices; NICE recommends Keytruda in NSCLC; Florida researcher indicted.
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Digital illustration of U.S., coronavirus

Stenzel says FDA making nine EUA decisions per day vs. one at outset of pandemic

Feb. 3, 2021
By Mark McCarty
The U.S. FDA is still struggling to keep up with the volume of diagnostic emergency use authorizations (EUAs), but it is not for want of effort. Tim Stenzel, director of the FDA’s Office of In Vitro Diagnostics and Radiological Health (OIR), said on the Feb. 3 testing town hall that the agency is processing nine such applications per day, a big jump over the rate of one per day in the early weeks of the COVID-19 pandemic.
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Coronavirus variants

Seegene develops COVID-19 test kit capable of detecting multiple variants

Feb. 3, 2021
By Gina Lee
HONG KONG – Seegene Inc. has developed a COVID-19 test kit that is able to both detect and identify multiple mutant variations of the virus. “Getting test results from the Allplex SARS-CoV-2 Variants Ⅰ Assay takes two hours, which is normally how long getting results from a PCR test takes,” a Seegene spokesperson told BioWorld.
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Regulatory front for Feb. 3, 2021

Feb. 3, 2021
By Mark McCarty
The latest global regulatory news, changes and updates affecting medical devices and technologies, including: Task force gives CAS screening another thumbs down; USPTO expands program with Japan’s, South Korea’s patent offices; Boston Sci recalls electrode for ICD due to risk of fracture; CDSCO posts lists of approved tests.
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Other news to note for Feb. 3, 2021

Feb. 3, 2021
Med-tech happenings, including deals and partnerships, grants, preclinical data and other news in brief: Ardent Health Services, Ams, Axim Biotech, Bendcare, Botanisol Analytics, Casenet, Centene, Color, Colossal Contracting, Congenica, Decipher, Epredia, Extra Horizon, Fujifilm, Gabriel Precision Oncology, Gpm, Histosonics, Inspiremd, McGinley Orthopedics, Medline, Meridian Bioscience, Mobile Heartbeat, Netsmart, New England Biolabs, Ocean Insight, Quantumdx, Veeva, Veracyte, Vizient, Zyter.
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U.S. vaccine illustration

U.S. lawmakers warned to prepare for worse days ahead in pandemic

Feb. 3, 2021
By Mari Serebrov
While the Biden administration’s America Rescue Plan began its journey through Congress Feb. 3 as the next U.S. effort to address the COVID-19 pandemic, lawmakers came together to identify steps to improve vaccine distribution and curb ongoing supply shortages.
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