Through the collaboration, the two companies will have the ability
to scale up production should one or more of Lilly's antibody
therapies prove receive regulatory approval, the companies said in a
statement.
Eli Lilly on Wednesday reported that a single infusion of its
experimental antibody treatment cut hospitalizations and emergency
room visits for clinical trial patients with moderate COVID-19.
"We are impressed with Lilly's data, in particular the reduction in
hospitalizations, and are enthusiastic about the potential for these
neutralizing antibodies as a therapeutic for COVID-19," David Reese,
Amgen's research and development chief, said in the statement.
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Eli Lilly had said it would discuss the interim data with global regulators,
including the U.S. Food and Drug Administration, and that discussions could also
include the possibility of an emergency use authorization.
(Reporting by Manas Mishra in Bengaluru; Editing by Maju Samuel)
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