60
Participants
Start Date
October 12, 2021
Primary Completion Date
April 20, 2023
Study Completion Date
July 28, 2023
Low-dose IL-2
After a 4-week screening period, patients received IL-2 at a dose of 1 million IU subcutaneously every other day. After the initiation of the therapy, patients could continue with concurrent medication but were prohibited from changing or adding immunosuppression therapy during the course of the study with a 12-week observational followed up.
Placebo
After a 4-week screening period, patients received placebo subcutaneously every other day. After the initiation of the therapy, patients could continue with concurrent medication but were prohibited from changing or adding immunosuppression therapy during the course of the study with a 12-week observational followed up.
Department of Rheumatology and Immunology, Peking University People's Hospital, Beijing
HeJing
OTHER