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BioWorld - Tuesday, January 27, 2026
Home » Topics » Infection » Coronavirus

Coronavirus
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Sinovac COVID-19 vaccine gets approved in China; doors opening elsewhere

Feb. 8, 2021
By David Ho and Gina Lee
HONG KONG – Sinovac Biotech Ltd.’s COVID-19 vaccine, Coronavac, received conditional approval for use by the general public from China’s National Medical Productions Administration, two days after filing for conditional market authorization.
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South African flag and syringe

South Africa shifts vaccination plan on SARS-CoV-2 variant data

Feb. 8, 2021
By Nuala Moran
LONDON – South Africa has decided against using the 1 million doses of Astrazeneca plc’s COVID-19 vaccine already in the country to start the rollout of its national vaccination program, in favor of opening a phase IIIb study of Johnson & Johnson’s single shot product. “Over the next few days, we expect to announce a plan to expedite vaccination using [J&J’s] investigational vaccine in health care professionals in South Africa,” said Glenda Gray, CEO of the South African Medical Research Council and chair of the country’s research committee on COVID-19.
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Regulatory actions for Feb. 8, 2021

Feb. 8, 2021
Regulatory snapshots, including global drug submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Anpac, Astrazeneca, Catapult, Elevar, Ellodi, Ideaya, Janssen, Passage, RDIF, Sinovac, Supernus, Viiv.
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Other news to note for Feb. 8, 2021

Feb. 8, 2021
Biopharma happenings, including deals and partnerships, grants, preclinical data and other news in brief: 4D Pharma, Atara, Azurity, Bayer, Chamishi, Elicio, Entera, Eton, Lineage, Moleculin, Nanoviricides, Navigo, Neurgain, Olix, Orion, Orpha, Q-State, Repligen, Seneca, Sigilon, Therapeutic Solutions, Unity.
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In the clinic for Feb. 8, 2021

Feb. 8, 2021
Clinical updates, including trial initiations, enrollment status and data readouts and publications: AC Immune, Avrobio, Cassava, Covaxx, Cue, Dong-A, Eiger, Erytech, Freeline, Jasper, Magenta, Sinovac, Uniqure, Veru.
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Regulatory front

FDA: Guidance coming to help with variants

Feb. 8, 2021
By Mari Serebrov
The latest global regulatory news, changes and updates affecting biopharma, including: CBO model touts savings of H.R. 3; FDA to ODAC: Are data ripe for 2nd TNBC Keytruda approval?; Fifth Circuit reiterates no liability remedy for generics; Consultant faces insider trading charges.
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Illustration of head, brain blood flow with Novaguide

Novasignal launches app to rapidly communicate cerebral ultrasound data

Feb. 5, 2021
By Mary Ellen Schneider
Novasignal Corp. has a launched a cloud-based app to provide alerts to clinicians directly from its cerebral ultrasound device. The new app allows physicians to get instant notifications from the company’s Novaguide device, a transcranial doppler ultrasound technology that allows for real-time assessment of blood flow in the brain by combining robotics and artificial intelligence (AI).
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IPO money

Lucira Health launches $153M IPO

Feb. 5, 2021
By Meg Bryant
Infectious diseases diagnostics company Lucira Health Inc. launched an IPO of 9 million shares of common stock at $17 per share, for expected gross proceeds of $153 million. Friday’s Wall Street debut was a show of confidence, upsized from an original plan to offer 7.8 million shares at $15 to $17. The Emeryville, Calif.-based company has granted the underwriters a 30-day option to acquire up to an additional 1,350,000 shares of common stock at the initial public offering price, less underwriting discounts and commissions.
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Chess board and pieces, blocks spelling out M&A

Earlysense distributes its remote monitoring tech to Hillrom

Feb. 5, 2021
By David Ho
HONG KONG – Earlysense Ltd. has sold a contact-free continuous monitoring technology to global med-tech provider Hillrom Holdings Inc. Ramat Gan, Israel-based Earlysense will receive licensing for all intellectual property and technology sold to Chicago-based Hillrom for use outside the hospital along with $30 million in cash, commercial milestone payments and a portion of Hillrom's equity investment
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Astrazeneca-COVID-19-vaccine-vials

Positive news: Astrazeneca vaccine still effective in B.1.1.7 SARS-CoV-2 variant

Feb. 5, 2021
By Nuala Moran
LONDON – A follow-up study of participants in the phase II/III U.K. trial of Astrazeneca plc’s COVID-19 vaccine has shown it remains effective against the new B.1.1.7 variant of SARS-CoV-2.
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