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BioWorld - Friday, March 24, 2023
Home » Topics » Infection » Coronavirus

Coronavirus
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Capsule with Swiss flag

Swiss biotech investment slipped 25% in 2019 as sector braced for COVID-19 disruption

April 21, 2020
By Cormac Sheridan
No Comments
DUBLIN – The Swiss biotech sector raised about CHF1.2 billion ($$1.2 billion) in equity investment in 2019, a significant downward dip on the last two years, but well ahead of its average annual raise of CHF800 million over the past decade, according to the newly published Swiss Biotech Report 2020.
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Australia and coronavirus

Australia’s biotech sector tests multiple agents to fight COVID-19

April 21, 2020
By Tamra Sami
No Comments
PERTH, Australia – The Australian Government is providing AU$13 million (US$8 million) to fast-track research into treatments for COVID-19, and a number of promising candidates are about to enter the clinic.
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Regulatory actions for April 21, 2020

April 21, 2020
No Comments
Regulatory snapshots, including global drug submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Alk-Abello, Bayer, Beigene, Boehringer Ingelheim, Hope, Myovant, Passage.
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Other news to note for April 21, 2020

April 21, 2020
No Comments
Biopharma happenings, including deals and partnerships, grants, preclinical data and other news in brief: Acerus, Adamis, Aikido, Allterum, Bayer, Biogen, Biosig, Cipher, Edesa, Forma, Galephar, Innovation, Merck, Mogrify, Novan, Novimmune, Opgen, Pharming, Polarityte, Redhill, Revive Therapeutics, Sangamo, Sun, Suono Bio, Twoxar Pharmaceuticals, Upsher-Smith, Vaxart, VBL, Viravaxx, Vivacelle.
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COVID-19 therapies will be needed by fall

April 21, 2020
By Mari Serebrov
No Comments
It’s all hands on deck as government agencies, researchers, startups, biopharma giants, health care workers and payers combine their resources to develop proven COVID-19 therapies that can be ready for market by fall when the pandemic is expected to pick up steam again in the U.S. and other northern reaches of the world.
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Regulatory front for April 21, 2020

April 21, 2020
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The latest global regulatory news, changes and updates affecting biopharma.
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vent-multiplexor.png

Vent Multiplexor’s ventilator-sharing device wins FDA nod for emergency use

April 20, 2020
By Meg Bryant
No Comments
The U.S. FDA has granted emergency use authorization (EUA) to New Haven, Conn., startup Vent Multiplexor LLC for its emergency rescue co-ventilation device. Developed in collaboration with Yale New Haven Hospital, the Vent Multiplexor enables individualized mechanical ventilation of two adults on a single ventilator – lessening demand for more critical care machines in the ongoing COVID-19 outbreak.
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Ortho-vitros-antibody-blood-test.png

Ortho Clinical Diagnostics scores win with total antibody test for COVID-19

April 20, 2020
By Liz Hollis
No Comments
The COVID-19 pandemic has moved rapidly over the past few weeks, and Ortho Clinical Diagnostics Inc. is doing its part to help during the crisis. To that end, the Raritan, N.J.-based company has worked to successfully secure an emergency use authorization (EUA) for its total antibody assay for COVID-19, the Vitros Immunodiagnostic Products Anti-SARS-CoV-2 total reagent pack and calibrators.
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Microscope image of SARS-CoV-2

Osang becomes first Korean company to win FDA emergency authorization

April 20, 2020
By Gina Lee
No Comments
HONG KONG – South Korea’s Osang Healthcare Co. Ltd. became the first Korean company to receive the U.S. FDA’s emergency use authorization (EUA) for its COVID-19 test kit. In a letter dated April 18, 2020, the FDA informed Osang of its authorization for the company’s Genefinder COVID-19 Plus Realamp Kit.
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Regulatory actions for April 20, 2020

April 20, 2020
No Comments
Regulatory snapshots, including global submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Cytosorbents, Endospan, Fosun Pharma, Foundation Medicine, Genosensor, Osang Healthcare.
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