drugset / Trial / NCT01215916

A Phase 1 Study in Patients With Solid Tumors

NCT01215916

Phase 1 Completed 39 enrolled Eli Lilly and Company
Non-randomizedParallel-groupOpen-labelTreatment

Summary

The primary objective of this study is to determine the maximum tolerated dose (MTD) regimen for the combination therapy of LY573636 and pemetrexed that may be safely administered to patients with a solid tumor that is not amenable to curative therapy.

Timeline

Start
2008-02
Primary completion
2011-12
Completion
2011-12

Drugs

EvaluationDrugModalityDoseRoute
Subject Pemetrexed Small molecule 375 mg/m2 Intravenous
Subject Pemetrexed Small molecule 500 mg/m2 Intravenous
Subject Tasisulam Small molecule Intravenous

Indications