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BioWorld - Wednesday, May 31, 2023
Home » Topics » Infection » Coronavirus

Coronavirus
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Regulatory actions for April 30, 2020

April 30, 2020
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Regulatory snapshots, including global drug submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Acasti, Akarx, Alpha Cognition, Annovis Bio, Banner Life Sciences, Biocardia, Dova, Galectin, Genmab, Glaxosmithkline, Inmed, Junshi, Marker, Medivir, Neon, Pharming, Seelos, Zentalis.
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Other news to note for April 30, 2020

April 30, 2020
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Biopharma happenings, including deals and partnerships, grants, preclinical data and other news in brief: Acelrx, Affibody, Ajinomoto, Aravive, Astrazeneca, Atreca, Bavarian Nordic, Beigene, Bioage Labs, Biosig, Bioinvent, Biostem, Cytodyn, Daewoong Pharmaceutical, Fujifilm Diosynth, Geovax, IGM Biosciences, Inovio, Just-Evotec, Ology, Oxford Biodynamics, PDS, Pfizer, Promis, Siga, Sprint, Sino Biological, Stabilitech, Taisho Pharmaceutical, Trio, Union, Vaxart, Viralclear, Wuxi, Xortx.
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In the clinic for April 30, 2020

April 30, 2020
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Clinical updates, including trial initiations, enrollment status and data readouts and publications: Agios, Bellus, Gilead, GSK, Janssen, Jazz, Leo, Lilly, Mallinckrodt, Mesoblast, Morphosys, Novartis, Palatin, Sanofi, Silence, Soligenix, Spectrum, Urogen, Vertex, Yuhan.
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Chronolife-Keesense-shirt.png

Chronolife scores win in Europe with Keesense remote health-monitoring platform

April 29, 2020
By Liz Hollis
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Artificial intelligence-focused Chronolife SAS, of Paris, has secured class IIa medical certification from the EU for its smart T-shirt, which has the new brand name Keesense. The reusable, washable T-shirt is designed for comfortable, round-the-clock use. It works by transmitting data to a paired smartphone app via Bluetooth.
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Regulatory front for April 29, 2020

April 29, 2020
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The latest global regulatory news, changes and updates affecting medical devices and technologies, including: Refocus Group, Venner Medical.
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Regulatory action for April 29, 2020

April 29, 2020
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Regulatory snapshots, including global submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Diatherix, Medtronic, Photopharmics, Psychemedics, Senseonics, Vuno.
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Other news to note for April 29, 2020

April 29, 2020
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Med-tech happenings, including deals and partnerships, grants, preclinical data and other news in brief: Alivecor, Bioiq, Canon Medical Systems, Centene, Current Health, Dexcom, DFP Healthcare Acquisitions, ELT Sight, Intersystems, Labcorp, Masimo, Matrix Medical Network, Mayo Clinic, Medable, Medical Diagnostic Laboratories, Medplace, Mindray, Proteogenix, Pure Health, Quest Diagnostics, Seasun, Soc Telemed, Tmk Manufacturing, Trinity Health, Vander-Bend, Windtree.
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BioWorld MedTech’s Orthopedics Extra for April 29, 2020

April 29, 2020
By Holland Johnson
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Keeping you up to date on recent developments in orthopedics, including: Physio support in COVID-19 recovery; Co-delivery of IL-10 and NT-3 to enhance spinal cord injury repair; European countries face a costly 23% increase in fragility fractures by 2030.
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Remdesivir capsule

Fauci calls remdesivir 'new standard of care' for COVID-19 as FDA works with Gilead to aid drug’s availability

April 29, 2020
By Michael Fitzhugh
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Following revelations that a randomized, placebo-controlled study of the Gilead Sciences Inc.’s antiviral, remdesivir, reduced time to recovery for hospitalized patients with "advanced" COVID-19, along with additional data from an open-label phase III trial from its maker, the FDA is "working with Gilead to figure out a mechanism to make this easily available to people who need it," Anthony Fauci, director of the NIH’s National Institute for Allergy and Infectious Diseases (NIAID), said April 29.
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Coronavirus and DNA

Capricor’s COVID-19 success gets FDA and market attention

April 29, 2020
By Lee Landenberger
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Six of six critically ill COVID-19 patients survived after being treated as compassionate care cases with Capricor Therapeutics Inc.’s lead candidate, an off-the-shelf cardiac cell therapy. The success prompted the FDA to review the data and approve the company’s expanded access protocol for treating as many as 20 more COVID-19 patients.
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