drugset / Trial / NCT00413777

Tolvaptan Open-label Pilot Efficacy, Tolerability, and Safety Study in Autosomal Dominant Polycystic Kidney Disease (ADPKD)

NCT00413777 ↗

RandomizedParallel-groupOpen-labelTreatment

Summary

This study's purpose is to evaluate the long-term safety of open-label tolvaptan regimens to determine the maximally-tolerated dose and acquire pilot efficacy data in patients with autosomal dominant polycystic kidney disease (ADPKD).

Timeline

Start
2005-12
Primary completion
2010-06
Completion
2010-06

Outcome

Met primary endpoint

paper Control TKV increased 5.8% versus 1.7%/yr for tolvaptan (P < 0.001 PMID 21903984 ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Tolvaptan Unknown 15 mg Oral
Subject Tolvaptan Unknown 30 mg Oral
Subject Tolvaptan Unknown 45 mg Oral
Subject Tolvaptan Unknown 60 mg Oral