drugset / Trial / NCT01358019

A Study of LY2523355 in Patients With Solid Cancer

NCT01358019

Phase 1 Completed 18 enrolled Kyowa Kirin, Inc.
NaSingle-groupOpen-labelTreatment

Summary

The primary objective of this study is to examine a recommended dose for subsequent phase trial(s), by the observation of the safety and toxicity profiles of LY2523355 in patients with advanced and/or metastatic cancer. The secondary objectives are to study the pharmacokinetics and antitumor effect.

Timeline

Start
2011-05
Primary completion
2013-01
Completion
2013-01

Drugs

EvaluationDrugModalityDoseRoute
Subject litronesib Small molecule 2 mg/m2
Subject litronesib Small molecule 4 mg/m2
Subject litronesib Small molecule 5 mg/m2

Indications