32
Participants
Start Date
August 1, 2020
Primary Completion Date
December 31, 2021
Study Completion Date
June 1, 2023
Anakinra
The active treatment group will receive anakinra 100 mg subcutaneously every 6-12 hours for a period of 10 days
Normal saline
The control group will receive normal saline placebo subcutaneously every 6-12 hours for period of 10 days
University of Alabama at Birmingham, Birmingham
University of Alabama at Birmingham
OTHER