A Phase 3 Randomized, Double-Blind, Placebo-Controlled Trial to Evaluate the Efficacy and Safety of LY3819253 Alone and in Combination With LY3832479 in Preventing SARS-CoV-2 Infection and COVID-19 in Skilled Nursing and Assisted Living Facility Residents and Staff; a NIAID and Lilly Collaborative Study
Latest Information Update: 08 Feb 2022
At a glance
- Drugs Bamlanivimab (Primary) ; Etesevimab (Primary)
- Indications COVID 2019 infections; SARS-CoV-2 acute respiratory disease
- Focus Registrational; Therapeutic Use
- Acronyms BLAZE-2
- Sponsors Eli Lilly and Company
- 16 Sep 2021 According to an Eli Lilly and Company Media Release, The U.S. Food and Drug Administration (FDA) has expanded the Emergency Use Authorization (EUA) for bamlanivimab 700 mg and etesevimab 1400 mg administered together to include post-exposure prophylaxis (PEP) in certain individuals for the prevention of SARS-CoV-2 infection.The expanded authorization is based on data from BLAZE-2
- 15 Jun 2021 retained actual pts number and Etesevimab as per NCT, no info of this and combination of two drugs Bamlanivimab and Etesevimab assessment in result incoming.Pls update further.
- 08 Jun 2021 Status changed from active, no longer recruiting to completed.