drugset / Trial / NCT01626209

A Phase I Study of BKM120 in Adult Chinese Patients With Advanced Solid Tumors

NCT01626209

Phase 1 Completed 32 enrolled Novartis Pharmaceuticals
Non-randomizedSingle-groupOpen-labelTreatment

Summary

Dose escalation study with a dose expansion phase, to evaluate safety, tolerability, pharmacokinetics and preliminary efficacy of two dose levels of BKM120 when administered orally.

Timeline

Start
2012-07
Primary completion
2014-04
Completion
2014-04

Drugs

EvaluationDrugModalityDoseRoute
Subject Buparlisib Small molecule 80 mg Oral
Subject Buparlisib Small molecule 100 mg Oral