At a glance
ClinicalIndex Comparison RecordPhase 3Completed· 277 enrolled
Drug / intervention
Anifrolumab +1 morebiological
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.
Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.
A Multicentre, Randomised, Double-blind, Placebo-controlled, Phase III Study Evaluating the Efficacy and Safety of Anifrolumab in Asian Participants With Active Systemic Lupus Erythematosus
In Brief
A Phase 3 clinical trial evaluating Anifrolumab and placebo for Active Systemic Lupus Erythematosus. Completed, enrolled 277 participants across 65 sites in 6 countries.
Detailed Summary
The purpose of this study is to evaluate the efficacy and safety of an intravenous treatment regimen of anifrolumab versus placebo in Asian participants with active systemic lupus erythematosus (SLE).
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsActive Systemic Lupus Erythematosus
CountriesChina, Hong Kong, Philippines, South Korea, Taiwan, Thailand
Collaborators--
Timeline
Phase 3CompletedFinished
20222023202420252026
First PostedJun 2021
Enrollment StartSep 2021
Primary CompletionApr 2025
Study CompletionJun 2025
TodayJul 2026
First PostedJun 18, 2021
Enrollment StartSep 13, 2021
Primary CompletionApr 7, 2025
Study CompletionJun 10, 2025
TodayJul 2, 2026
Enrollment to primary: 3.6 yearsPosted 5.0 years ago
Interventions
Anifrolumabbiological
Intravenous infusion (IV)
placebodrug
Intravenous infusion (IV)