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Clinical Trial Summary

Primary Objective • To assess the dose response relationship between RGLS4326 and ADPKD biomarkers Secondary Objectives - To characterize the pharmacokinetic (PK) properties of RGLS4326 in plasma and urine - To assess the safety and tolerability of RGLS4326


Clinical Trial Description

This is a Phase 1b, open-label, adaptive design dose-ranging study to evaluate ADPKD biomarkers, PK, safety, tolerability, and pharmacodynamics (PD) of RGLS4326 administered via SC injection to patients with ADPKD. The goal is to assess the dose response relationship between RGLS4326 and ADPKD biomarkers. The study will consist of three sequential cohorts with approximately 18 to 27 subjects total. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04536688
Study type Interventional
Source Regulus Therapeutics Inc.
Contact
Status Completed
Phase Phase 1
Start date October 13, 2020
Completion date November 12, 2021

See also
  Status Clinical Trial Phase
Completed NCT00428948 - Tolvaptan Phase 3 Efficacy and Safety Study in ADPKD Phase 3