drugset / Trial / NCT01106508

A Dose Finding and Safety Study of Oral LEQ506 in Patients With Advanced Solid Tumors

NCT01106508 ↗

Phase 1 Completed 57 enrolled Novartis Pharmaceuticals
NaSingle-groupOpen-labelTreatment

Summary

This first-in-human dose-escalation study is to characterize the safety, tolerability, pharmacokinetics and pharmacodynamics of LEQ506 given orally on a daily dosing schedule in patients with advanced solid tumors.

Timeline

Start
2010-10
Primary completion
2015-06
Completion
2015-06

Drugs

EvaluationDrugModalityDoseRoute
Subject LEQ506 Small molecule — Oral