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Early use of anakinra reduces risk of mortality for patients with COVID-19 pneumonia, reduces ICU admission and increases likelihood of full recovery


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- Day 28 full results from the SAVE-MORE study show early treatment with anakinra plus SOC (standard of care) reduced mortality by 55% and reduced average time until ICU (intensive care unit) discharge by four days
- Day 28 full results from the SAVE-MORE study show early treatment with anakinra plus SOC (standard of care) reduced mortality by 55% and reduced average time until ICU (intensive care unit) discharge by four days
- In patients treated with anakinra plus SOC, overall clinical status improved by 64% compared to those treated with SOC alone
- The SAVE-MORE trial, conducted by the Hellenic Institute for the Study of Sepsis, is the first large, pivotal randomised controlled trial to specifically evaluate a target patient population with COVID-19 at risk of progressing and demonstrating the benefit of earlier intervention with anakinra for the prevention of disease progression and reduced risk of mortality ....

United States , Kostenloser Wertpapierhandel , Maria Kruse , Evangelosj Giamarellos Bourboulis , Paula Treutiger , Guido Oelkers , European Shock Society , World Health Organization , Hellenic Institute For The Study Of Sepsis , Kapodistrian University Of Athens , European Sepsis Alliance , Hellenic Institute , Internal Medicine , Infectious Diseases , Kapodistrian University , European Sepsis , Progression Scale , Odds Ratio , Guided Anakinra Treatment , Severe Respiratory Failure , Professor Giamarellos Bourboulis , Familial Mediterranean , Systemic Juvenile Idiopathic Arthritis , Adult Onset Still , Intensive Care Units , North America ,

Claritas (Formerly Kalytera Therapeutics) Cites Breakthrough Data by Massachusetts General ...


Press release content from Globe Newswire. The AP news staff was not involved in its creation.
Claritas (Formerly Kalytera Therapeutics) Cites Breakthrough Data by Massachusetts General .
Claritas Pharmaceuticals, Inc.March 2, 2021 GMT
SAN FRANCISCO, March 02, 2021 (GLOBE NEWSWIRE) Claritas Pharmaceuticals, Inc. (formerly Kalytera Therapeutics, Inc.) (TSX VENTURE: KLY and OTC: KALTF) (the “Company” or “Claritas”) today announced that compelling data demonstrating that nitric oxide achieved viral clearance in severe and critical COVID-19 patients validates the potential of the Company’s proprietary nitric oxide releasing compound, R-107, as a therapy for coronavirus and COVID-19 infection.
Breakthrough Data with Nitric Oxide in COVID-19 ....

United States , North Carolina , Uppsala Lan , Robert Farrell , Salvatore Cuzzocrea , Uppsala University , Company Or Claritas , Kalytera Therapeutics Inc , Claritas Pharmaceuticals , University Of Messina , European Shock Society , Novan Inc , Salzman Group , Claritas Pharmaceuticals Inc , Venture Exchange , Regulation Services Provider , Kalytera Therapeutics , Nitric Oxide , Massachusetts General Hospital , Know Bio , Antiviral Research , Utah State , Mass General , Clarita President , Although Claritas , Public Health ,