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BioWorld - Monday, April 27, 2026
Home » Topics » Infection » Coronavirus

Coronavirus
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Patient in hospital bed

Tubulin test: Veru coming through as COVID-19 queue debated

Sep. 7, 2022
By Randy Osborne
Wall Street trimmed shares of Veru Inc. (NASDAQ:VERU) by upwards of 20% in the wake of an editorial published Aug. 23 in The New England Journal of Medicine publication NEJM Evidence. The opinion piece, by two critical-care pulmonologists, added verve to the debate about the efficacy of drugs for people hospitalized with COVID-19.
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Regulatory actions for Sept. 7, 2022

Sep. 7, 2022
Regulatory snapshots, including global drug submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Alvotech, Amylyx, Aston, Astrazeneca, Bausch + Lomb, Novaliq, Novavax, Tenaya.
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In the clinic for Sept. 7, 2022

Sep. 7, 2022
Clinical updates, including trial initiations, enrollment status and data readouts and publications: Abivax, Alaunos, Bavarian Nordic, Boehringer Ingelheim, Clarity, Dizal, Dyne, Immutep, Innovent, Ironwood, Iveric, Jacobio, Laekna, Mannkind, Regeneron, Sanofi, Yingli, Zymeworks.
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Disintegrating coronavirus
Infection

Tetra Bio-Pharma and Cellvera to develop ARDS-003 in combination with favipiravir for COVID-19

Sep. 7, 2022
Tetra Bio-Pharma Inc. has signed an agreement with Cellvera Global Holdings LLC for the co-development of ARDS-003 (onternabez) as a combination product with Qifenda (favipiravir) 400 mg, a commercial-stage broad-spectrum antiviral drug.
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Immune

Biovaxys announces in vivo study of pan-sarbecovirus vaccine

Sep. 7, 2022
Biovaxys Technology Corp. has announced that Millipore-Sigma, the contract manufacturer for its preclinical viral vaccine program, has completed the bioproduction and batch release endotoxin screening of BVX-1021, the company's vaccine for SARS-CoV, which is being used in the collaboration with The Ohio State University (OSU) to develop a pan-sarbecovirus vaccine.
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Green approved stamp

China clears two new COVID-19 boosters for emergency use

Sep. 6, 2022
By Doris Yu
China’s NMPA has granted emergency use authorization for two COVID-19 vaccines as boosters, Cansino Biologics Inc.’s inhaled vaccine Convidecia Air and Livzon Pharmaceutical Group Inc.’s recombinant protein vaccine. Convidecia Air is an aerosolized adenovirus type 5 vector-based vaccine. It is the first inhaled COVID-19 vaccine to be approved globally, according to Cansino.
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Regulatory actions for Sept. 6, 2022

Sep. 6, 2022
Regulatory snapshots, including global drug submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Azurity, Bayer, Boehringer, Immuneering, Intellia, Moderna, Novavax, Y-mabs.
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Regulatory actions for Sept. 2, 2022

Sep. 2, 2022
Regulatory snapshots, including global drug submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Amneal, Aston, Biontech, Genentech, Immusoft, Moderna, Pfizer, Roche, Sanofi.
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Other news to note for Sept. 2, 2022

Sep. 2, 2022
Biopharma happenings, including deals and partnerships, grants, preclinical data and other news in brief: Bridge, Celsion, Ensysce, Helsinn, I-Cordis, Juniper, MC2, Quotient.
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In the clinic for Sept. 2, 2022

Sep. 2, 2022
Clinical updates, including trial initiations, enrollment status and data readouts and publications: Algernon, Algo, Anaptysbio, Avacta, Axsome, Coya, Pliant, Reveragen, Santhera, Vaxart, Vyluma, Werewolf.
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