Drugs / Bebtelovimab

Trials 3

PhaseRegistry idDatesIndicationSponsorStatusOutcome
Phase 21 trial
Phase 2 NCT04634409 Oct 2020 → Jul 2021 COVID-19 Eli Lilly and Company Completed Mixed
Phase 2/31 trial
Phase 2/3 NCT04427501 Jun 2020 → Feb 2023 COVID-19 Eli Lilly and Company Completed No outcome recorded
Phase 41 trial · 1 missed
Phase 4 NCT04790786 Mar 2021 → Jun 2022 COVID-19 Erin McCreary Terminated Missed primary

News releases announcing trial results or a regulatory action · 1

DateIssuerRelease
2022-02-11 Eli Lilly and Company Regulatory Lilly's bebtelovimab receives Emergency Use Authorization for the treatment of mild-to-moderate COVID-19 lilly.com ↗
The U.S. Food and Drug Administration (FDA) has issued an Emergency Use Authorization (EUA) for bebtelovimab, an antibody that demonstrates neutralization against the Omicron variant, Eli Lilly and Company (NYSE: LLY) announced today.

Evidence & citations 5 cited values

Every value below carries the sentence it was read from. 4 sources stand behind the page.

FieldValueCited text
Known as Bebtelovimab ClinicalTrials.gov intervention name — accepted as the source's own label NCT04634409 ↗
1

NCT04790786 ↗

Known as LY-CoV1404 ChEMBL registry synonym — accepted as the source's own label CHEMBL4802210 ↗
Known as LY3853113 ClinicalTrials.gov intervention name — accepted as the source's own label NCT04427501 ↗
Modality Monoclonal antibody “The monoclonal antibody of bebtelovimab” NCT04790786 ↗
Route Intravenous “Administered IV” NCT04427501 ↗