drugset / Trial / NCT00756223

Phase I Study of BI 831266 in Patients With Advanced Solid Tumours

NCT00756223 ↗

Phase 1 Completed 25 enrolled Boehringer Ingelheim
RandomizedParallel-groupOpen-labelTreatment

Summary

The main objective of this trial is to provide safety data in terms of drug-related adverse events for the recommendation of the dose for further trials in the development of BI 831266. Secondary objectives are the collection of antitumour efficacy data and the determination of the pharmacokinetic and pharmacodynamic profile of BI 831266.

Timeline

Start
2008-11
Primary completion
2010-10
Completion
—

Drugs

EvaluationDrugModalityDoseRoute
Subject BI 831266 Unknown 32 mg Intravenous
Subject BI 831266 Unknown 130 mg Intravenous

Indications