drugset / Trial / NCT02809183

Evaluation of TRC101 in Subjects With Chronic Kidney Disease and Metabolic Acidosis

NCT02809183 ↗

Phase 1/2 Completed 135 enrolled Tricida, Inc.
RandomizedParallel-groupDouble-blindTreatment

Summary

This was a double-blind, placebo-controlled, parallel-design, 6-arm, fixed dose study. The study enrolled 135 adult male and female subjects with Stage 3 or 4 chronic kidney disease and low serum bicarbonate levels. The study was conducted in two parts. In Part 1 study drug dosing (TRC101 or placebo) continued for 14 days twice daily (BID). In Part 2 study drug dosing (TRC101 or placebo) continued for 14 days once daily (QD). The maximum study duration per subject was anticipated to be up to 42 days.

Timeline

Start
2016-03
Primary completion
2016-11
Completion
2016-11

Drugs

EvaluationDrugModalityDoseRoute
Subject Veverimer Other / unclassified 1.5 g Oral
Subject Veverimer Other / unclassified 3 g Oral
Subject Veverimer Other / unclassified 4.5 g Oral
Subject Veverimer Other / unclassified 6 g Oral

Indications