drugset / Trial / NCT00550381

Study Evaluating the Safety, Tolerability, and Pharmacokinetics (PK) of HKI-357 Administered Orally to Healthy Subjects

NCT00550381 ↗

Phase 1 Completed 72 enrolled Wyeth is now a wholly owned subsidiary of Pfizer
RandomizedSingle-groupDouble-blindTreatment

Summary

The purpose of this study is to assess the safety, tolerability, and pharmacokinetics of single doses of HKI-357 administered to healthy subjects.

Timeline

Start
2008-01
Primary completion
2008-03
Completion
2008-03

Drugs

EvaluationDrugModalityDoseRoute
Comparator HKI-357 Small molecule 10 mg Oral
Comparator HKI-357 Small molecule 20 mg Oral
Comparator HKI-357 Small molecule 40 mg Oral
Comparator HKI-357 Small molecule 80 mg Oral
Comparator HKI-357 Small molecule 160 mg Oral
Comparator HKI-357 Small molecule 240 mg Oral
Comparator HKI-357 Small molecule 400 mg Oral
Comparator HKI-357 Small molecule 640 mg Oral
Comparator HKI-357 Small molecule 960 mg Oral

Indications

No indication recorded.