drugset / Trial / NCT02685462
Pharmacokinetic and Safety Study of Cenicriviroc and HMG-CoA Reductase Inhibitors, Caffeine and Digoxin
Non-randomizedParallel-groupOpen-labelTreatment
Summary
This is a Phase 1, Open-Label, 3-Period, Single-sequence, Drug-drug Interaction Study in Healthy Subjects to Assess the Effect of Cenicriviroc on the Pharmacokinetics (PK) of HMG-CoA Reductase Inhibitors \[Rosuvastatin (ROS), Atorvastatin (ATO) and Simvastatin (SIM)\], Caffeine and Digoxin
Timeline
- Start
- 2016-01-31
- Primary completion
- 2016-02-23
- Completion
- 2016-02-23
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Atorvastatin | Small molecule | 20 mg | — |
| Subject | Caffeine | Small molecule | 200 mg | — |
| Subject | Digoxin | Other / unclassified | 0.25 mg | — |
| Subject | Rosuvastatin | Small molecule | 20 mg | — |
| Subject | Simvastatin | Small molecule | 20 mg | — |
Indications
No indication recorded.