The U.S. government will pay Eli Lilly $375 million to secure an initial supply of 300,000 vials of bamlanivimab, the pharma company’s experimental COVID-19 drug pending emergency approval by the Food and Drug Administration (FDA).
“The U.S. is experiencing a surge in COVID-19 cases and associated hospitalizations, and we believe bamlanivimab could be an important therapeutic option that can bring value to the overall healthcare system, as it has shown a potential benefit in clinical outcomes with a reduction in viral load and rates of symptoms and hospitalizations,” David A. Ricks, Lilly’s chairman and CEO, said in a statement.
It will be used in antibody treatment for “high-risk” COVID-19 patients with mild-to-moderate symptoms, the drugmaker said. If the FDA grants it an Emergency Use Authorization (EUA), the patients will not have to pay for the medicine.
“The initial agreement is for delivery over the two months following an EUA and also provides the option for the U.S. government to purchase up to an additional 650,000 vials through June 30, 2021,” the company’s statement read.
While vaccines reduce the risk of infection by training the body’s immune system to recognize and combat the virus, antibody drugs are designed to mimic or enhance the body’s immune response to fight infection, producing a temporary effect that could help prevent infected patients from developing worse symptoms.