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BioWorld - Thursday, January 1, 2026
Home » Topics » Infection » Coronavirus

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Other news to note for July 14, 2022

July 14, 2022
Biopharma happenings, including deals and partnerships, grants, preclinical data and other news in brief: Act, Adipopharma, Altamira, Anthos, Bicycle, Coagulant, Comera, Currax, Epicentrx, Genscript, Hemab, Hoth, Immunoprecise, Intron, Mymd, Nilogen, Novo Nordisk, Relief, Renovacor, Roche, Siga, SQZ, Swedish Orphan, Teva, Turn, Vivus.
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In the clinic for July 14, 2022

July 14, 2022
Clinical updates, including trial initiations, enrollment status and data readouts and publications: Atara, Bio-Thera, Endevica, Evolus, Glenmark, Humanigen, Hutchmed, Optinose, Pluristem, Rhythm, Sanotize, Vaxcyte, Xortx.
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Box of Astrazeneca COVID-19 vaccine vials

Humanigen’s COVID-19 vaccine underperforms as AZ matches the mRNAs

July 13, 2022
By Lee Landenberger
Lenzilumab, Humanigen Inc.’s lead candidate, undershot statistical significance on the primary endpoint in the U.S. NIH-sponsored ACTIV-5/BET-B study of treating hospitalized COVID-19 patients. The Short Hills, N.J.-based company’s stock (NASDAQ:HGEN) crumpled in the wake of the results.
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Regulatory actions for July 13, 2022

July 13, 2022
Regulatory snapshots, including global drug submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Basilea, Bellus, Byondis, Citius, Cyxone, Dyne, Fresenius, Greenwich, Novartis, Y-mabs.
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U.S. Capitol building, Washington D.C.

FDA’s Califf says delays in user fee legislation could trigger layoffs

July 12, 2022
By Mark McCarty
Legislation that would renew the U.S. FDA’s user fee programs is stuck in process on Capitol Hill, a predicament that seems to resist resolution to date. FDA commissioner Robert Califf said on a July 12 webinar that the FDA “is a decision-making machine” that is reliant on both user fees and congressional appropriations, and that a failure on the part of Congress to act on user fee legislation may force the agency to halt new hires and possibly lay off some FDA staff.
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Regulatory actions for July 12, 2022

July 12, 2022
Regulatory snapshots, including global drug submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Anthos, Arcutis, Can-Fite, Iterum, Lipocine, Perrigo, Pfizer, SCG.
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In the clinic for July 12, 2022

July 12, 2022
Clinical updates, including trial initiations, enrollment status and data readouts and publications: ADC, Aquestive, Biomica, Exelixis, Freeline, Genentech, Hansa, Immunocore, Ionis, Macrogenics, Mediwound, Moderna, Novo Nordisk, Pliant, Sanofi, Swedish Orphan, Telix, Tonix.
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European Union map and coronavirus

European regulators recommend second COVID-19 booster dose, as Moderna files fresh data from omicron shot

July 11, 2022
By Richard Staines
European regulators and health experts have recommended a second booster dose of mRNA COVID-19 vaccines for people between 60 and 79 years of age and for vulnerable people with medical conditions, as Moderna Inc. filed fresh data from its omicron subvariant-adapted shot.
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In the clinic for July 11, 2022

July 11, 2022
Clinical updates, including trial initiations, enrollment status and data readouts and publications: Inventiva, Moleculin, Myrtelle, Optinose, Regenxbio.
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Regulatory actions for July 11, 2022

July 11, 2022
Regulatory snapshots, including global drug submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Alimera, Horizon, MGC, Puma, Siga.
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