drugset / Trial / NCT01049893

Dose Finding, Safety and Tolerability Study for AC220 to Treat Advanced Solid Tumors

NCT01049893

Phase 1 Completed 45 enrolled Daiichi Sankyo
NaSingle-groupOpen-labelTreatment

Summary

AC220 will be administered as a once daily oral solution given continuously as 28-day treatment cycles, without food and without any rest periods, as long as there is no evidence of disease progression or unacceptably severe adverse events (AEs) related to the study drug.

Timeline

Start
2010-01
Primary completion
2011-11
Completion
2011-11

Drugs

EvaluationDrugModalityDoseRoute
Subject Quizartinib Small molecule 90 mg Oral
Subject Quizartinib Small molecule 135 mg Oral

Indications