RecruitingPhase 1NCT07228364
Safety, Tolerability and Pharmacokinetics of AZD1613 in Adults With Autosomal Dominant Polycystic Kidney Disease
Studying Autosomal dominant polycystic kidney disease
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- AstraZeneca
- Intervention
- AZD1613 - Part A(drug)
- Enrollment
- 40 enrolled
- Eligibility
- 18-65 years · All sexes
- Timeline
- 2025 – 2027
Study locations (15)
- Research Site, Birmingham, Alabama, United States
- Research Site, Loma Linda, California, United States
- Research Site, Jacksonville, Florida, United States
- Research Site, Orlando, Florida, United States
- Research Site, Lenexa, Kansas, United States
- Research Site, Baltimore, Maryland, United States
- Research Site, Rochester, Minnesota, United States
- Research Site, San Antonio, Texas, United States
- Research Site, Chengdu, China
- Research Site, Hangzhou, China
- Research Site, Nanjing, China
- Research Site, Shanghai, China
- Research Site, Wuhan, China
- Research Site, Xiamen, China
- Research Site, London, United Kingdom
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
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