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BioWorld - Sunday, May 22, 2022
Home » Topics » Infection » Coronavirus

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COVID-19 research illustration

US NIH COVID-19 technologies going global

May 12, 2022
By Mari Serebrov
No Comments
In an effort to increase global access to COVID-19 technologies, the World Health Organization’s COVID-19 Technology Access Pool and the Medicines Patent Pool finalized a licensing agreement May 12 with the U.S. NIH for research tools, early stage vaccines and diagnostics.
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Regulatory actions for May 12, 2022

May 12, 2022
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Regulatory snapshots, including global submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Accelus, Cepheid, Medmira, Remedee Labs, Wysa.
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Regulatory actions for May 12, 2022

May 12, 2022
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Regulatory snapshots, including global drug submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Amicus, Ascletis, Cue, Eli Lilly, Immuron, Incyte, Iterum, Kiromic, Regulus, Spine, Veru.
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Other news to note for May 12, 2022

May 12, 2022
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Biopharma happenings, including deals and partnerships, grants, preclinical data and other news in brief: CSL, Enveric, Gain, Juvenescence, Neximmune, Propanc, Rakovina, Selah, Sound, Vifor, Zealand.
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In the clinic for May 12, 2022

May 12, 2022
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Clinical updates, including trial initiations, enrollment status and data readouts and publications: Abbvie, Arcellx, Cognition, Genentech, Glyscend, Inovio, Medicenna, Mind, Myeloid, Rhovac, Sanofi, Scilex, Spine.
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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
No Comments
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
No Comments
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
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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
No Comments
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
No Comments
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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