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  • COVID-19 Treatment :...

COVID-19 Treatment : Eli Lilly's Bebtelovimab no longer authorized by USFDA

Ruchika SharmaWritten by Ruchika Sharma Published On 2022-12-01T15:30:40+05:30  |  Updated On 2022-12-01T15:31:01+05:30
COVID-19 Treatment : Eli Lillys Bebtelovimab no longer authorized by USFDA

Eli Lilly and its authorized distributors have paused the commercial distribution of the monoclonal antibody until further notice from the agency.

US: Eli Lilly and Co's COVID-19 drug bebtelovimab is not currently authorized for emergency use in the United States, the Food and Drug Administration said, citing it is not expected to neutralize the dominant BQ.1 and BQ.1.1 subvariants of Omicron.Wednesday's announcement takes away authorization from the last COVID-19 monoclonal antibody treatment, leaving Pfizer Inc's antiviral...

US: Eli Lilly and Co's COVID-19 drug bebtelovimab is not currently authorized for emergency use in the United States, the Food and Drug Administration said, citing it is not expected to neutralize the dominant BQ.1 and BQ.1.1 subvariants of Omicron.

Wednesday's announcement takes away authorization from the last COVID-19 monoclonal antibody treatment, leaving Pfizer Inc's antiviral drug Paxlovid, Merck's Lagevrio, and Gilead Sciences' Veklury as treatments for the disease, besides convalescent plasma for some patients.

AstraZeneca Plc's monoclonal antibody Evusheld is also authorized for protection against COVID-19 infection in some people.

Eli Lilly and its authorized distributors have paused the commercial distribution of the monoclonal antibody until further notice from the agency, while the U.S. government has also paused fulfillment of any pending requests under its scheme to help uninsured and underinsured Americans access the drug.

The drug, which was discovered by Abcellera and commercialized by Eli Lilly, received an authorization from the FDA in February.

Read also: Eli Lilly unveils DCGI approved Ramiven in India for early stage breast cancer

BQ.1 and BQ.1.1 have become the dominant strains in the United States after a steady increase in prevalence over the last two months, surpassing Omicron's BA.5 sub-variant, which had driven cases earlier in the year.

The subvariants accounted for around 57% of the cases nationally, as per government data last week.

Read also: Eli Lilly bags USFDA emergency use nod for COVID drug Bebtelovimab

Eli Lilly Eli Lilly news COVID 19 coronavirus bebtelovimab Omicron Abcellera 
Source : Reuters
Ruchika Sharma
Ruchika Sharma

    M.Com

    Ruchika joined Medical Dialogue as an Desk Editor for the Business Section in 2019. She covers all the updates in the Pharmaceutical field, Policy, Insurance, Business Healthcare, Medical News, Health News, Pharma News, Healthcare and Investment. She has completed her B.Com from Delhi University and then pursued postgraduation in M.Com. She can be contacted at editorial@medicaldialogues.in Contact no. 011-43720751

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