drugset / Trial / NCT02809183
Evaluation of TRC101 in Subjects With Chronic Kidney Disease and Metabolic Acidosis
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| 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 |