Condition: Autosomal Dominant Polycystic Kidney Disease · Sponsor: AstraZeneca
A study to investigate safety, tolerability, and pharmacokinetics of AZD1613 following subcutaneous or intravenous administration in participants with autosomal dominant polycystic kidney disease (ADPKD).
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 | Not Yet Recruiting |
| Research Site | Loma Linda, California, United States | Not Yet Recruiting |
| Research Site | Jacksonville, Florida, United States | Recruiting |
| Research Site | Orlando, Florida, United States | Recruiting |
| Research Site | Lenexa, Kansas, United States | Recruiting |
| Research Site | Baltimore, Maryland, United States | Not Yet Recruiting |
| Research Site | Rochester, Minnesota, United States | Recruiting |
| Research Site | San Antonio, Texas, United States | Not Yet Recruiting |
| Research Site | Chengdu, China | Not Yet Recruiting |
| Research Site | Hangzhou, China | Not Yet Recruiting |
| Research Site | Nanjing, China | Recruiting |
| Research Site | Shanghai, China | Not Yet Recruiting |
+ 3 more locations — full list on the registry record.
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This page is independently generated by Eichor from the public ClinicalTrials.gov record and re-synced daily. It is not the sponsor's official website unless claimed. Nothing here is medical advice; eligibility is always determined by the study team — talk to your own doctor first.
Source record: clinicaltrials.gov/study/NCT07228364