drugset / Trial / NCT07228364

Safety, Tolerability and Pharmacokinetics of AZD1613 in Adults With Autosomal Dominant Polycystic Kidney Disease

NCT07228364 ↗

Phase 1 Recruiting 40 enrolled AstraZeneca
RandomizedParallel-groupQuadruple-blindTreatment

Summary

A study to investigate safety, tolerability, and pharmacokinetics of AZD1613 following subcutaneous or intravenous administration in participants with autosomal dominant polycystic kidney disease (ADPKD).

Timeline

Start
2025-11-10
Primary completion
2027-01-26
Completion
2027-01-26

Drugs

EvaluationDrugModalityDoseRoute
Subject AZD1613 Unknown — Subcutaneous