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BioWorld - Monday, February 9, 2026
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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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Regulatory actions for May 9, 2022

May 9, 2022
Regulatory snapshots, including global drug submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Johnson & Johnson, Myovant, Pfizer.
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Other news to note for May 9, 2022

May 9, 2022
Biopharma happenings, including deals and partnerships, grants, preclinical data and other news in brief: Aqilion, Aracari, Brii, Compass, Cumberland, Gain, IGM, Insilico, Jemincare, Neurelis, Orion, Psybio, Verity, Virpax.
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In the clinic for May 9, 2022

May 9, 2022
Clinical updates, including trial initiations, enrollment status and data readouts and publications: Acer, Amylyx, Anthos, Citius, Evofem, KVK-Tech, Relief, Scilex, Sen-Jam, Sorrento.
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Cloud data sharing illustration
Medtech Forum

Going digital, where exactly is the value?

May 6, 2022
By Catherine Longworth
In response to the COVID-19 pandemic, health systems around the world are looking to digital technologies to support health delivery but where exactly can these technologies have the most impact? At the Medtech Forum in Barcelona, European leaders gathered to discuss practical examples of how digital tools can help make health systems more efficient.
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Syringe with Johnson & Johnson logo

Better than nothing: FDA limits use of J&J COVID-19 vaccine

May 6, 2022
By Michael Fitzhugh
A risk of rare but potentially life-threatening blood clots in combination with low platelet levels after a jab of Johnson & Johnson's Janssen COVID-19 vaccine has convinced the U.S. FDA to limit its use. The vaccine is now authorized in the U.S. only for adults who wouldn't otherwise be vaccinated and those who can't or shouldn't, for medical reasons, get another approved vaccine. Through March 18, 2022, the FDA and CDC have identified 60 confirmed cases, including nine fatal cases of the condition, called thrombosis with thrombocytopenia syndrome – a rate of 3.23 cases per million doses of vaccine administered.
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Regulatory actions for May 6, 2022

May 6, 2022

Regulatory snapshots, including global drug submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Astrazeneca, Bio Products, Daiichi, Incyte, Jiangsu Recbio, Kempharm, Moleculin, Newsoara, Palisade, Vistagen, Xortx.


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Other news to note for May 6, 2022

May 6, 2022
Biopharma happenings, including deals and partnerships, grants, preclinical data and other news in brief: Agile, Arca, Avalo, Biomarin, CSL, Novartis.
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