drugset / Trial / NCT01919398

A Study of LY2940680 in Japanese Participants With Advanced Cancers

NCT01919398

Phase 1 Completed 19 enrolled Eli Lilly and Company
NaSingle-groupOpen-labelTreatment

Summary

The primary purpose of this study is to assess the safety and tolerability of LY2940680 up to the global recommended dose in Japanese participants with advanced solid cancers.

Timeline

Start
2013-08
Primary completion
2016-05
Completion
2017-06-28

Drugs

EvaluationDrugModalityDoseRoute
Subject taladegib Small molecule 100 mg Oral
Subject taladegib Small molecule 200 mg Oral
Subject taladegib Small molecule 400 mg Oral

Indications