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(CMRX) - Chimerix's DSTAT Shows Promising Results In First Cohort Of COVID-19 Study

(CMRX) - Chimerix's DSTAT Shows Promising Results In First Cohort Of COVID-19 Study
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Acute Lung Injury Market Driven By Commence Bio, FirstString Research, Altor BioScience, CompleGen, Histocell, Windtree Therapeutics, S-Evans Biosciences

Acute Lung Injury Market Driven By Commence Bio, FirstString Research, Altor BioScience, CompleGen, Histocell, Windtree Therapeutics, S-Evans Biosciences

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Monoclonal Antibodies Show Promise Treating COVID-19

There is particular interest in monoclonal antibody agents to determine whether their immune suppressive effects can reduce the immediate and long-term impact of COVID-19.

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Global Acute Respiratory Distress Syndrome (ARDS) Epidemiology Forecast to 2030 - ResearchAndMarkets.com - Press Release

Global Acute Respiratory Distress Syndrome (ARDS) Epidemiology Forecast to 2030 - ResearchAndMarkets.com ResearchAndMarkets.com s offering. This Acute Respiratory Distress Syndrome (ARDS) - Epidemiology Forecast-2030 report delivers an in-depth understanding of the disease, historical and forecasted Acute Respiratory Distress Syndrome (ARDS) epidemiology in the United States, EU5 (Germany, France, Italy, and United Kingdom), and Japan. Acute Respiratory Distress Syndrome (ARDS) Epidemiology Perspective The disease epidemiology covered in the report provides historical as well as forecasted epidemiology segmented by Total Incident Population of ARDS, Severity-specific Incidence of ARDS, and Incidence of ARDS by Risk Factors scenario of Acute Respiratory Distress Syndrome (ARDS) in the 7MM covering the United States, EU5 countries (Germany, France, Italy, Spain, and United Kingdom) and Japan from 2017 to 2030.

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Results of NIH-sponsored ACTIV-3 trial published

E-Mail IMAGE: Colorized scanning electron micrograph of an apoptotic cell (green) heavily infected with SARS-COV-2 virus particles (orange), isolated from a patient sample. Image captured at the NIAID Integrated Research Facility (IRF). view more Credit: NIAID Preliminary results of a phase 3, randomized, placebo-controlled clinical trial testing the investigative monoclonal antibody LY-CoV555 in hospitalized COVID-19 patients were published today in the New England Journal of Medicine. The antibody did not provide clinical benefit compared to placebo. The trial, which had been halted to new enrollment in late October following a recommendation by the independent Data and Safety Monitoring Board (DSMB), is part of the Accelerating COVID-19 Therapeutic Interventions and Vaccines (ACTIV) program. The trial is sponsored by the National Institute of Allergy and Infectious Diseases (NIAID), part of the National Institutes of Health.

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