drugset / Trial / NCT02684799

Pharmacokinetic and Safety Study of Cenicriviroc and Acid Reducing Agents When Dosed Alone or in Combination

NCT02684799

Phase 1 Completed 48 enrolled Tobira Therapeutics, Inc.
RandomizedParallel-groupOpen-labelTreatment

Summary

This is a Phase 1, Single and Multiple-Dose, Open-Label Study in Healthy Subjects to Assess the Effect of the Acid Reducing Agents, Omeprazole and Famotidine, on the PK of CVC

Timeline

Start
2016-01-31
Primary completion
2016-04-11
Completion
2016-04-11

Drugs

EvaluationDrugModalityDoseRoute
Subject Cenicriviroc Small molecule 150 mg
Comparator Famotidine Other / unclassified 40 mg
Comparator Omeprazole Other / unclassified 40 mg

Indications

No indication recorded.