Eli Lilly and Company's bebtelovimab receives Emergency Use Authorization for the treatment of mild-to-moderate COVID-19
Posted:
FDA has authorized bebtelovimab for emergency use for certain non-hospitalized patients with mild-to-moderate COVID-19 at high risk of progression to severe disease for whom alternative COVID-19 treatment options approved or authorized by FDA are not accessible or clinically appropriate Bebtelovimab neutralizes Omicron as demonstrated by pseudovirus and authentic virus data.
Memora helps health systems and payers to incorporate AI-driven workflow-automation technology.
The platform sends patient-reported concerns and data to clinical care team members and offers two-way communication and support, the company said.
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Information included payment details such as credit card or bank account numbers and insurance info ranging from Medicaid and Medicare IDs to policy numbers and claims. Secure EHR data was not accessed.
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