Condition: Polymyositis, Dermatomyositis · Sponsor: AstraZeneca
The purpose of this multicenter, randomized, placebo-controlled and double-blind study is to evaluate the efficacy and safety of subcutaneous anifrolumab compared with placebo on the overall disease activity in participants with moderate to severe Idiopathic Inflammatory Myopathies (IIM) \[polymyositis (PM) or dermatomyositis (DM)\] while receiving standard of care (SoC) treatment.
This description comes directly from the study's public registry record.
AstraZeneca Clinical Study Information Center · 1-877-240-9479 · information.center@astrazeneca.com
Always discuss trial participation with your own doctor first.
| Research Site | Phoenix, Arizona, United States | Not Yet Recruiting |
| Research Site | Irvine, California, United States | Recruiting |
| Research Site | Aurora, Colorado, United States | Recruiting |
| Research Site | Denver, Colorado, United States | Not Yet Recruiting |
| Research Site | New Haven, Connecticut, United States | Recruiting |
| Research Site | Washington D.C., District of Columbia, United States | Withdrawn |
| Research Site | Boca Raton, Florida, United States | Recruiting |
| Research Site | Boynton Beach, Florida, United States | Withdrawn |
| Research Site | Gainesville, Florida, United States | Withdrawn |
| Research Site | Margate, Florida, United States | Suspended |
| Research Site | Miami, Florida, United States | Withdrawn |
| Research Site | Miami, Florida, United States | Recruiting |
+ 224 more locations — full list on the registry record.
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