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BioWorld - Thursday, March 30, 2023
Home » Topics » Infection » Coronavirus

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Other news to note for April 24, 2020

April 24, 2020
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Biopharma happenings, including deals and partnerships, grants, preclinical data and other news in brief: Adaptvac, AGC, Agastiya, Axovant, Emergent, Johnson & Johnson, Epimab, Hoth, Voltron, Nexstim, Sanofi, Scancell, Sumitomo Dainippon, Takeda, Orifarm, Tracon.
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In the clinic for April 24, 2020

April 24, 2020
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Clinical updates, including trial initiations, enrollment status and data readouts and publications: Astrazeneca, Bellicum, Boehringer, Chugai, GSK, Janssen, Kiromic, Merck, Novartis, Novocure, Noxxon, Sanofi, TC Biopharma, Tonix, UCB.
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Regulatory actions for April 23, 2020

April 24, 2020
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Regulatory snapshots, including global drug submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Algernon, Amidebio, Caladrius, CNS Pharma, Cstone, Immuneoncia, Immunomedics, Merck and Co., Rafael, Revive, Samsung Biologics, Vitalis.
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CMS, ONC offer enforcement discretion for EHR rules

April 23, 2020
By Mark McCarty
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The U.S. Centers for Medicare and Medicaid Services (CMS) and the Office of the National Coordinator for Health Information Technology (ONC) said that they will offer enforcement discretion for their respective final rules for electronic health records (EHRs), a nod to the COVID-19 pandemic. The term of the delays of compliance for several of these rules is not uniform, ranging from “late 2020” to “spring 2021,” and vendors thus will have to be vigilant to ensure they do not cross any compliance tripwires.
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Perspectum launches study of post-COVID-19 organ damage

April 23, 2020
By Annette Boyle
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Oxford, U.K.-based Perspectum Diagnostics Ltd. is recruiting patients for a study to determine the degree of damage sustained by major organs following infection with the SARS-CoV-2 virus. The company will use its multiparametric magnetic resonance imaging (MRI) devices and other means to evaluate post-COVID-19 organ damage, track healing and evaluate impact on survivors.
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Cytovale gets new BARDA funding to assess early sepsis detection technology for COVID-19

April 23, 2020
By Meg Bryant
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Cytovale Inc., a San Francisco-based medical technology company, has snagged an additional $3.83 million in funding from the U.S. Department of Health and Human Services’ Biomedical Advanced Research and Development Authority (BARDA) to conduct a pilot study of its Rapid Sepsis Diagnostic System for patients with potential respiratory infections, including SARS-CoV-2, the novel coronavirus responsible for COVID-19. The patented technology, which can diagnose sepsis in less than 10 minutes, could speed up triaging and treatment of critically ill patients suspected of having the life-threatening condition.
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DNA-based Spartan Cube to test for COVID-19 in Canada

April 23, 2020
By David Godkin
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TORONTO – A portable DNA-based test kit developed by Ottawa-based Spartan Bioscience Inc. has received Health Canada approval for COVID-19 testing – this at a time when hospitals are under enormous pressure to meet increased testing demand.
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Regulatory action for April 23, 2020

April 23, 2020
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Regulatory snapshots, including global submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Agilent, Baxter, Biocomposites, Cagent Vascular, Mevion.
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Other news to note for April 23, 2020

April 23, 2020
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Med-tech happenings, including deals and partnerships, grants, preclinical data and other news in brief: Axogen, Aytu Bioscience, Biocartis Group, Biolidics, Caredx, Carestream Health, Daxor, Electromedical Technologies, Encision, Enzo Biochem, Exogenesis, IBD, Lumex, Medmira, Muranaka, Nanomesh, Neucomed Group, Opentrons, Predictive Oncology, Quidel, Rewalk, Seco, Sengenics, Siemen Healthineers, Signifier Medical Technologies, Spineway, Synteract, Tearlab, Trinetx, Veracyte, Webbdx, Wytcote, Zeus Scientific, Zymo.
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Premature posting of remdesivir data raises doubts for use in COVID-19

April 23, 2020
By Jennifer Boggs
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Shares of Gilead Sciences Inc. were dented April 23 after reports surfaced that its antiviral drug, remdesivir, failed to improve the condition of patients with COVID-19.
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