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BioWorld - Friday, January 2, 2026
Home » Topics » Infection » Coronavirus

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Evusheld carton and vials

Full data published on Evusheld, Astrazeneca’s ‘last MAb standing’ in COVID-19

April 21, 2022
By Randy Osborne
Astrazeneca plc led the handful of firms rolling out COVID-19-related news, as the company said detailed results from the Provent phase III pre-exposure prophylaxis (prevention) trial with Evusheld (tixagevimab and cilgavimab), were published in the New England Journal of Medicine, the “culmination of about 19 months of pretty intensive work,” said Mark Esser, vice president of microbial sciences.
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Regulatory actions for April 21, 2022

April 21, 2022
Regulatory snapshots, including global submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Clarius Mobile Health.
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Other news to note for April 21, 2022

April 21, 2022
Biopharma happenings, including deals and partnerships, grants, preclinical data and other news in brief: Aim Immunotech, Biogen, Blue Water Vaccines, Humanigen, Immvira, Roche, Samsung Bioepis, Selva, Sihuan Pharma, Tonix, Xortx, Xuansheng Pharma.
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In the clinic for April 21, 2022

April 21, 2022
Clinical updates, including trial initiations, enrollment status and data readouts and publications: Arcturus, Bavarian Nordic, Clover, Fibrogen, Navidea, Otonomy, Snipr, Trevena, Ultragenyx, Windtree.
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US booster study next after Arcturus’ self-amplifying mRNA COVID-19 vaccine hits endpoints

April 20, 2022
By Jennifer Boggs
Arcturus Therapeutics Holdings Inc. reported that ARCT-154, its self-amplifying mRNA COVID-19 vaccine, showed efficacy of 55% against infection and 95% efficacy against severe disease, meeting the primary and key secondary endpoints of the ongoing phase I/II/III trial. While the company’s stock (NASDAQ:ARCT) regained much of its initial 25% drop to close the day, investors continue to await further data to determine where Arcturus’ vaccine will fit in with available COVID-19 vaccines.
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Regulatory actions for April 20, 2022

April 20, 2022
Regulatory snapshots, including global submissions and approvals, clinical trial approvals and other regulatory decisions and designations: The Orthopaedic Implant Company, Zeiss.
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Coronavirus, mRNA and syringe

ACIP warns against COVID-19 ‘booster fatigue’

April 20, 2022
By Mari Serebrov
The U.S. COVID-19 vaccine program is at risk of “booster fatigue,” which will undermine public confidence in the vaccines, several members of the CDC’s Advisory Committee on Immunization Practices (ACIP) said April 20 as they met to discuss the future of the vaccines. Rather than relying on boosters, “we need to use our expertise to advocate for something that’s better,” something that resolves the ill effects of COVID-19, whether it’s mild or severe, said Lynn Bahta, an immunization program clinical consultant for the Minnesota Department of Health.
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Regulatory actions for April 20, 2022

April 20, 2022
Regulatory snapshots, including global drug submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Adicet, Astrazeneca, Axsome, Aytu, Daiichi Sankyo, Hansa, Innovative Cellular, Merck, Navidea, Novavax, NTC, Ribomic, Serum Institute, Takeda..
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Other news to note for April 20, 2022

April 20, 2022
Biopharma happenings, including deals and partnerships, grants, preclinical data and other news in brief: Abbvie, Aclipse, Aptinyx, Benevolentai, Diamyd, Dragonfly, Endevica, Heat, Hoth, Neuropore, Nextcure, PDS, Pharmacyte, Soligenix, Therapeutic Solutions.
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In the clinic for April 20, 2022

April 20, 2022

Clinical updates, including trial initiations, enrollment status and data readouts and publications: Acadia, Amgen, Beigene, Bioage, Biorestorative, Clover, Cyclacel, Kempharm, Moderna, Neuraly, Synaptogenix, TFF, Urovant.


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