drugset / Trial / NCT00831506

Dimebon (PF-01913539)-Digoxin Drug-Drug Interaction Study In Healthy Subjects

NCT00831506

Phase 1 Completed 12 enrolled Pfizer Medivation, Inc. · collab
RandomizedCrossoverQuadruple-blindTreatment

Summary

This study has been designed to confirm, in healthy subjects, the lack of a clinically important pharmacokinetic interaction between Dimebon, at the proposed maximum commercial dose of 20 mg TID (administered every 8 hours), and digoxin (Lanoxin®) 0.125 mg QD, a sensitive P-gp substrate recommended by FDA.

Timeline

Start
2009-02
Primary completion
2009-05
Completion
2009-05

Drugs

EvaluationDrugModalityDoseRoute
Subject Digoxin Other / unclassified 0.125 mg
Subject Latrepirdine Small molecule 20 mg