drugset / Trial / NCT01161069

A Study To Evaluate The Safety And Tolerability Of Different Doses Of PF-03049423 In Healthy Adult Volunteers And Healthy Older Volunteers

NCT01161069 ↗

Phase 1 Completed 48 enrolled Pfizer
RandomizedParallel-groupDouble-blind

Summary

The purpose this study is to evaluate the safety and toleration of PF-03049423 following multiple dose administration as an oral solution to healthy young adult volunteers and healthy elderly volunteers. The study will also evaluate the pharmacokinetics of PF-03049423 after multiple dose administration to healthy young adult volunteers and healthy elderly volunteers. The study will also explore the relationship between blood pressure (supine and standing) and PF-03049423 concentration.

Timeline

Start
2009-08
Primary completion
2009-12
Completion
2009-12

Drugs

EvaluationDrugModalityDoseRoute
Comparator PF-03049423 Small molecule 2.5 mg Oral
Comparator PF-03049423 Small molecule 6 mg Oral
Comparator PF-03049423 Small molecule 7.5 mg Oral
Comparator PF-03049423 Small molecule 10 mg Oral
Comparator PF-03049423 Small molecule 12 mg Oral

Indications

No indication recorded.