A North Carolina drugmaker plans to test its experimental antiviral drug in patients who have Ebola, after getting authorization from regulators at the Food and Drug Administration.

Topics:  north carolina   ebola   food   drug   administration   test   
BING NEWS:
  • Abbott, BioMérieux, Cepheid, Roche, Others Gain FDA 510(k) Clearances in December
    The FDA granted marketing clearances for infectious disease tests, updates to a digital pathology system, and immunoassays for chronic diseases.
    01/22/2025 - 2:53 am | View Link
  • FDA authorises marketing of Inflammatix’s blood test for sepsis diagnosis
    Inflammatix CEO and co-founder Tim Sweeney said: "The fundamental problem with existing tests is an outdated focus on labelling patients as 'septic or not.' But sepsis is a syndro ...
    01/21/2025 - 9:03 pm | View Link
  • Osang Healthcare Nabs FDA Clearance for COVID-19, Flu Combo Tests
    The QuickFinder COVID-19/Flu Antigen Self-Test and the QuickFinder COVID-19/Flu Antigen Pro Test detect SARS-CoV-2, influenza A, and influenza B in swab specimens and provide results within 15 minutes ...
    01/21/2025 - 8:56 am | View Link
  • Offering quick way for ERs to treat a deadly condition, South Bay company scores FDA OK
    Sepsis, the leading cause of death in U.S. hospitals killing about 350,000 people annually, is an extreme response to an infection, with patients showing up in ERs with a cough, fever and rapid heart ...
    01/21/2025 - 12:33 am | View Link
  • FDA grants breakthrough designation to PreludeDx’s DCIS test
    The US Food and Drug Administration (FDA) has granted breakthrough device designation to PreludeDx's DCISionRT test, a risk assessment tool for ductal carcinoma in situ (DCIS), also known as Stage 0 ...
    01/16/2025 - 9:17 pm | View Link
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