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 Poland
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 Poland