Condition: Primary Membranous Nephropathy · Sponsor: AstraZeneca
The purpose of this study is to assess the safety, tolerability, pharmacokinetic, and efficacy of surovatamig administered by subcutaneous injection in adult participants with primary membranous nephropathy.
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 | Los Angeles, California, United States | Not Yet Recruiting |
| Research Site | Iowa City, Iowa, United States | Not Yet Recruiting |
| Research Site | Bethesda, Maryland, United States | Not Yet Recruiting |
| Research Site | New York, New York, United States | Not Yet Recruiting |
| Research Site | Houston, Texas, United States | Recruiting |
| Research Site | Houston, Texas, United States | Not Yet Recruiting |
| Research Site | Ieper, Belgium | Not Yet Recruiting |
| Research Site | Bordeaux, France | Not Yet Recruiting |
| Research Site | Créteil, France | Withdrawn |
| Research Site | Lyon, France | Not Yet Recruiting |
| Research Site | Nantes, France | Not Yet Recruiting |
| Research Site | Nîmes, France | Not Yet Recruiting |
+ 10 more locations — full list on the registry record.
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Source record: clinicaltrials.gov/study/NCT07571746