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BioWorld - Sunday, May 17, 2026
Home » Topics » Infection » Coronavirus

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U.S. Capitol and $100 bills

US lawmakers question budget fulcrum for ARPA-H, NIH

May 11, 2022
By Mari Serebrov
With its focus on transformative high-risk, high-reward research to drive biomedical breakthroughs, the new Advanced Research Projects Agency for Health (ARPA-H) may be a good concept, but it shouldn’t come at the expense of increased investment in basic research at the NIH, according to the bipartisan leadership of U.S. House appropriators.
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Inovio_CELLECTRA-devices-5-11.png

New CEO Shea to lead Inovio’s shift to COVID-19 vaccine booster strategy

May 11, 2022
By Jennifer Boggs
Newly appointed President and CEO Jackie Shea looks to have her work cut out for her, as Inovio Pharmaceuticals Inc. decided to ditch its phase II/III COVID-19 vaccination trial in favor of pursuing a booster strategy with INO-4800. That update, disclosed during Inovio’s first-quarter earnings late May 10 alongside a likely delay in filing for approval of HPV immunotherapy candidate VGX-3100, sent the stock (NASDAQ:INO) falling 27% May 11. Over the past year, shares have fallen more than 70%.
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Regulatory actions for May 11, 2022

May 11, 2022
Regulatory snapshots, including global drug submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Abbvie, Eisai, Gilead, Kadmon, Moleculin, Neogene, Novo Nordisk, Turning Point, Zai Lab.
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Other news to note for May 11, 2022

May 11, 2022
Biopharma happenings, including deals and partnerships, grants, preclinical data and other news in brief: Alvotech, Anges, Beckley, Bioasis, Corbus, Dare, Eiger, Entrada, Incannex, Inmune, Lophora, Mycrodose, Neuramedy, Rallybio, Rational.
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Digital illustration of U.S., coronavirus

Contamination at root of class I recall of Mesa Biotech’s Accula COVID test

May 10, 2022
By Mark McCarty
The in vitro diagnostics industry has turned in an impressive response to the COVID-19 pandemic, but a few problems are bound to surface. The U.S. FDA reported May 10 that the Accula test by San Diego-based Mesa Biotech Inc. has been recalled due to contamination of test materials at the manufacturing site, a problem that could lead to false negative findings with the test.
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US Oversight report sheds light on Emergent GMP issues

May 10, 2022
By Mari Serebrov
A congressional investigation into COVID-19 vaccine manufacturing failures at Emergent Biosolutions Inc. unveiled more troubling issues at the company’s Bayview facility in Baltimore, which had been awarded a lucrative U.S. government contract to produce vaccines for Johnson & Johnson.
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Vaccine administration

Second booster dose increases immunity, according to Cov-Boost data

May 10, 2022
By Nuala Moran
First results from the U.K. Cov-Boost trial, looking at responses to a fourth dose of an mRNA COVID-19 vaccine, show that antibody levels increase more than after the third dose, confirming the precautionary move to give the most vulnerable a second COVID-19 booster in advance of immune response data being available.
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Regulatory actions for May 10, 2022

May 10, 2022
Regulatory snapshots, including global drug submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Acer, Elpiscience, Logicbio, Resverlogix, Selection, Teva, Therapeutics Solutions.
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Other news to note for May 10, 2022

May 10, 2022
Biopharma happenings, including deals and partnerships, grants, preclinical data and other news in brief: Aum, Blade, Bristol, Celsion, Comera, Cortexyme, Dyadic, Evotec, FSD, Ibio, Merck, Modex, Novosteo, Opko, Pfizer, Roche, Venus.
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US FDA to consider lower efficacy for kids’ vaccine

May 9, 2022
By Mari Serebrov
The U.S. FDA’s efficacy bar for COVID-19 vaccines for the youngest children may be lower than the 50% required for the adult vaccines, according to Peter Marks, director of the agency’s Center for Biologics Evaluation and Research.<
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