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Morning Briefing

Summaries of health policy coverage from major news organizations

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Wednesday, Nov 11 2020

Full Issue

Supplies Of Eli Lilly's COVID Antibody Treatment Expected To Be Strained

Limited amounts of the drug and other logistical challenges could hamper the federal government to fairly distribute the newly approved treatment.

The Washington Post: Trump Officials Promise Fair Distribution Of New Covid-19 Antibody Drug, But Limited Supply And Logistical Problems Loom 

Trump administration officials Tuesday promised to fairly and swiftly distribute the first covid-19 treatment that helps to protect people with mild illness from developing severe symptoms. But the drug’s extremely limited supply and logistical difficulties in administering it could restrict how many people get access to it. The Eli Lilly & Co. drug is similar to an experimental treatment President Trump received when he was infected with the novel coronavirus. It is a laboratory-brewed antibody that imitates the immune system’s attack on the virus. (Wan, 11/10)

The Hill: Health Officials To Begin Distribution Of Eli Lilly Antibody Drug This Week

The federal government will begin distributing Eli Lilly's coronavirus antibody treatment this week, but supplies will be limited and getting the drug into infected patients will be a challenge, officials said. The drug itself is administered through an IV infusion that takes more than an hour and requires another hour of observation afterward, officials said. (Weixel, 11/10)

Also —

Stat: For Eli Lilly's Covid-19 Treatment, A Dosing Discrepancy Causes Confusion

Some clinicians are confused about the best dosing for Eli Lilly’s new Covid-19 treatment, which the Food and Drug Administration approved for emergency use on Monday. The drug is a monoclonal antibody, a lab-concocted version of what our bodies produce to fight off the new coronavirus. (Boodman, 11/10)

Fox News: Lilly’s Antibody IV Infusions For Coronavirus Patients To Present ‘Unique Challenges,’ Top Officials Say

While Eli Lilly’s investigational monoclonal antibody drug, bamlanivimab, just received FDA emergency approval to treat mild coronavirus patients, top officials voiced concerns over its challenging IV infusion process. “We anticipate that initially, there will be challenges for the health care system in administering IV infusions to infected patients,” Dr. Janet Woodcock, therapeutics lead for Operation Warp Speed, told reporters over a call on Tuesday. (Rivas, 11/10)

Stat: FDA Requires Lilly To Address Quality Control At Plant Making Covid-19 Drug

The Food and Drug Administration is requiring Eli Lilly (LLY) to hire consultants to test batches and vet quality-testing data at a manufacturing plant where its Covid-19 antibody treatment is being made, a mandate that comes after the agency found quality control problems during two separate inspections over the past year. (Silverman, 11/10)

This is part of the Morning Briefing, a summary of health policy coverage from major news organizations. Sign up for an email subscription.
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