Condition: Rheumatoid Arthritis · Systemic Lupus Erythematosus · Sponsor: AstraZeneca
This open-label, Phase I study will assess the safety and tolerability of surovatamig and characterise its PK and PD following subcutaneous administration to participants with RA or SLE.
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| Research Site | Birmingham, Alabama, United States | Withdrawn |
| Research Site | Fullerton, California, United States | Recruiting |
| Research Site | St Louis, Missouri, United States | Not Yet Recruiting |
| Research Site | Allen, Texas, United States | Recruiting |
| Research Site | Mesquite, Texas, United States | Recruiting |
| Research Site | Birtinya, Australia | Recruiting |
| Research Site | Clayton, Australia | Recruiting |
| Research Site | Edegem, Belgium | Recruiting |
| Research Site | Leuven, Belgium | Not Yet Recruiting |
| Research Site | Liège, Belgium | Recruiting |
| Research Site | Porto Alegre, Brazil | Not Yet Recruiting |
| Research Site | Salvador, Brazil | Not Yet Recruiting |
+ 21 more locations — full list on the registry record.
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Source record: clinicaltrials.gov/study/NCT07201558