drugset / Trial / NCT02746926

A Study Comparing Amounts of Tafamidis (PF-06291826) in the Blood Without Food in Healthy Volunteers

NCT02746926

Phase 1 Completed 12 enrolled Pfizer
RandomizedCrossoverOpen-labelBasic science

Summary

3 different formulations and doses of tafamidis will be compared. Subjects will be fasted for each test and every subject will test all 3 different formulations. After swallowing tafamidis, tafamidis blood concentrations will be measured periodically for 8 days. After 14 days, subjects will take a different formulation of tafamidis and tafamidis blood concentrations will be measured periodically for 8 days. After another 14 days, the last formulation will be tested in the same way.

Timeline

Start
2016-04-29
Primary completion
2016-07-15
Completion
2016-07-15

Drugs

EvaluationDrugModalityDoseRoute
Subject Tafamidis Unknown 48.8 mg Oral
Subject Tafamidis Unknown 61 mg Oral
Subject Tafamidis Unknown 80 mg Oral

Indications

No indication recorded.