drugset / Trial / NCT03487913

The ELiSA Study - Evaluation of Lixivaptan in Subjects With Autosomal Dominant Polycystic Kidney Disease

NCT03487913 ↗

Phase 2 Completed 31 enrolled Palladio Biosciences
Non-randomizedParallel-groupOpen-labelTreatment

Summary

This is a Phase 2, open-label, parallel-group, multiple dose study designed to evaluate the pharmacokinetics, pharmacodynamics, safety and tolerability of multiple doses of lixivaptan in Autosomal Dominant Polycystic Kidney Disease subjects with chronic kidney disease (CKD) in stages CKD1, CKD2 or CKD3.

Timeline

Start
2018-09-14
Primary completion
2019-12-02
Completion
2020-02-11

Publications

  • Results Shusterman NH, Hogan LC, Pellegrini L: Effect of lixivaptan on pharmacokinetic (PK) and pharmacodynamic (PD) end points in patients with autosomal dominant polycystic kidney disease (ADPKD) in the ELiSA Study (PA-102) [Abstract]. J Am Soc Nephrol 30, 2019 (abstract supplement issue): page 339.

Drugs

EvaluationDrugModalityDoseRoute
Subject Lixivaptan Small molecule — Oral