drugset / Trial / NCT02346890

A Phase 1 Study to Examine the Effect of Renvela on the Pharmacodynamics of AZD1722

NCT02346890

Phase 1 Completed 16 enrolled Ardelyx AstraZeneca · collab
RandomizedCrossoverOpen-labelTreatment

Summary

The study is designed to evaluate safety, tolerability, pharmacodynamics and pharmacokinetics of AZD1722 in healthy volunteers taking Renvela.

Timeline

Start
2013-04
Primary completion
2013-04
Completion
2013-04

Drugs

EvaluationDrugModalityDoseRoute
Subject Tenapanor Small molecule 15 mg
Subject sevelamer Other / unclassified 800 mg

Indications

No indication recorded.