Subcutaneous Anifrolumab in Adult Patients With Systemic Lupus Erythematosus
Condition(s) studied
Investigational drug(s) / intervention(s)
Medi-546: Patients will have IP administered or will self-administer IP under supervision by site staff at Week 0 and Week 1 and, for patients participating in the OLE period, at Week 52. For weekly doses coinciding with subsequent on-site visits, patients will also have IP administered or will self-administer IP under supervision by site staff, and in addition will receive a set of kits (including back-up kits) for at-home administration.
Placebo: Solution for injection in aPFS
Study summary
The purpose of this study is evaluating the efficacy and safety of SC antifrolumab in adult patients with moderate -to-severe SLE despite receiving standard therapy
Eligibility
Primary outcome measure(s)
- British Isles Lupus Assessment Group-based Composite Lupus Assessment (BICLA) response — At week 52
BICLA response is a composite binary endpoint whereby responders are defined by meeting all of the following criteria: * Improvement from baseline in disease activity as measured by BILAG-2004. Improvement is defined as a reduction of all baseline BILAG-2004 A to B/C/D and baseline BILAG-2004 B to C/D and no BILAG-2004 worsening in other organ systems, where worsening is defined as ≥ 1 new BILAG-2004 A or ≥ 2 new BILAG 2004 B. * No worsening from baseline in SLEDAI-2K, where worsening is defined as an increase from baseline of \> 0 points in SLEDAI-2K. * No worsening from baseline in the patient's lupus disease activity, where worsening is defined as an increase ≥ 0.30 points on a 3-point PGA VAS.
Trial sites (140)
| Facility | City | Region | Status |
|---|---|---|---|
| Research Site | Birmingham | Alabama | |
| Research Site | Paradise Valley | Arizona | |
| Research Site | Phoenix | Arizona | |
| Research Site | El Cajon | California | |
| Research Site | Fullerton | California | |
| Research Site | Hemet | California | |
| Research Site | La Mesa | California | |
| Research Site | Los Angeles | California | |
| Research Site | Menifee | California | |
| Research Site | Upland | California | |
| Research Site | Aurora | Colorado | |
| Research Site | Brandon | Florida | |
| Research Site | Clearwater | Florida | |
| Research Site | Clearwater | Florida | |
| Research Site | Miami | Florida | |
| Research Site | Tampa | Florida | |
| Research Site | Tampa | Florida | |
| Research Site | Idaho Falls | Idaho | |
| Research Site | Flint | Michigan | |
| Research Site | Lansing | Michigan | |
| Research Site | Newark | New Jersey | |
| Research Site | Las Cruces | New Mexico | |
| Research Site | Brooklyn | New York | |
| Research Site | Manhasset | New York | |
| Research Site | New York | New York | |
| Research Site | Potsdam | New York | |
| Research Site | Charlotte | North Carolina | |
| Research Site | Charlotte | North Carolina | |
| Research Site | Oklahoma City | Oklahoma | |
| Research Site | Pittsburgh | Pennsylvania | |
| Research Site | Reading | Pennsylvania | |
| Research Site | Memphis | Tennessee | |
| Research Site | Grapevine | Texas | |
| Research Site | Ciudad de Buenos Aires | Argentina | |
| Research Site | La Plata | Argentina | |
| Research Site | Mendoza | Argentina | |
| Research Site | Pergamino | Argentina | |
| Research Site | Quilmes | Argentina | |
| Research Site | Rosario | Argentina | |
| Research Site | Salta | Argentina |
+ 100 more sites — see the full list on the official registry below.
More AstraZeneca trials in the UK
Other trials for the same condition
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT04877691 on ClinicalTrials.gov ↗ ← All trials in the UK