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BioWorld - Thursday, May 14, 2026
Home » Topics » Infection » Coronavirus

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Other news to note for Dec. 10, 2021

Dec. 10, 2021
Med-tech happenings, including deals and partnerships, grants, preclinical data and other news in brief: Cambridge Orthopaedic, Eurofins, Exthera, Leica, Predicate HPG, Surgicalone, Tianrong, Wilton Management.
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Regulatory actions for Dec. 10, 2021

Dec. 10, 2021
Regulatory snapshots, including global drug submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Acer, Aprea, Bayer, Brii, Cytodyn, Cytokinetics, Heron, Intercept, Nrx, Ocugen, Reata, Sesen, VBI.
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Other news to note for Dec. 10, 2021

Dec. 10, 2021
Biopharma happenings, including deals and partnerships, grants, preclinical data and other news in brief: Abbvie, Atai, Altasciences, Biotheranostics, Candel, Cara, CB, Eli Lilly, Enteris, Hologic, Incyte, Iteos, Novozymes, Regor, Relay, Springworks, SWK, Synergia, Syndax, Tryptage, Xortx.
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Map of Europe

EIB issues $22M loan for rapid COVID-19 PCR test

Dec. 9, 2021
By Catherine Longworth
The European Investment Bank (EIB) is continuing a streak of investments in the med-tech space, signing a €20 million (US$22 million) loan agreement with Midiagnostics NV, to scale-up a new rapid COVID-19 PCR test. Leuven, Belgium-based Midiagnostics is developing a rapid PCR test for SARS-CoV-2, which can achieve an accuracy speed 20 times faster than classic PCR machines. A nasopharyngeal swab sample is transferred on a PCR testcard, from which the results are read by a compact reader. Pilot programs for the test began at Brussels Airport this month, with a market launch pegged for Spring 2022.
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Antibodies attacking SARS-CoV-2 virus

Brii Biosciences wins China's first approval for COVID-19 MAb therapy

Dec. 9, 2021
By David Ho
A cocktail of monoclonal neutralizing antibodies developed by Brii Biosciences Ltd. has become “the first locally-discovered and approved SARS-CoV-2 target-specific treatment in China, through a randomized, double-blind and placebo-controlled trial,” Rogers Luo, president and general manager of greater China at the company, told BioWorld. The NMPA approved a combination of Brii’s amubarvimab and romlusevimab as a treatment for both adults and pediatric patients, ages 12 to 17, with mild and “normal type” COVID-19 at high risk for progression to severe disease, including hospitalization or death.
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Cansino partners with Aerogen for inhalable COVID vaccine

Dec. 9, 2021
By Gina Lee
Cansino Biologics Inc. has entered a development and commercial supply partnership with Aerogen Ltd. for an inhalable version of its COVID-19 vaccine, Convidecia, also known as Ad5-nCoV. Cansino will combine Convidecia with Aerogen’s vibrating mesh aerosol drug delivery technology to produce a consistent droplet size for optimal lung deposition. The technology delivers up to six times more medication to the lungs compared to jet nebulizers. It also enables consistency and drug denaturing to improve efficacy. Cansino and Aerogen did not disclose the deal’s commercial terms.
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Health professional recording info from patient

Smacked by COVID-19: Recruitment to UK’s cancer trials plummets 60%

Dec. 9, 2021
By Nuala Moran
LONDON – New figures underline the devastating effect the pandemic is having on cancer clinical research, with recruitment to U.K. studies falling by 60%. A total of 27,734 patients were recruited in 2020/21, compared to an average of 67,057 in the three years previously. Over those three years, recruitment had been on the rise, going from 61,810 in 2017/18 to 71,709 in 2019/20, according to figures compiled by the Institute of Cancer Research in London.
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3D Euro symbol

Apogenix raises $29M to push COVID-19 drug into phase III

Dec. 9, 2021
By Richard Staines
As Omicron spreads throughout Europe there’s a pressing need for new therapies that could reduce the burden on hospitals by preventing COVID-19 symptoms from escalating to a critical point. Apogenix GmbH, of Heidelberg, Germany, is pushing a potential new therapy into phase III that could be added to the armamentarium against COVID-19 with €20.7 million (US$23.4 million) government funding.
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Glass globe
In vitro diagnostics on the rise

Regulatory flux, patent law issues negatively impacting IVD market

Dec. 9, 2021
By Mark McCarty
Makers of vitro diagnostics (IVDs) are facing several significant challenges in the next few years, thanks to existing and impending revisions to a number of regulatory frameworks. There are other considerations that are adding to the headwinds, such as a poor patent protection environment in the U.S., the net effect of which is to make life unusually miserable for developers of these tests.
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Regulatory actions for Dec. 9, 2021

Dec. 9, 2021
Regulatory snapshots, including global drug submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Aytu, Bioinvent, Biontech, Cybin, Cytodyn, Daré, Moderna, Neurop, Nuvation, Pfizer, Saol, Supernus.
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