drugset / Trial / NCT00701324

BI 811283 in Various Solid Tumours

NCT00701324 ↗

Phase 1 Completed 124 enrolled Boehringer Ingelheim
RandomizedOpen-labelTreatment

Summary

The main objective of this trial is to provide safety data in terms of drug-related adverse events (AE) for the recommendation of the dose for further trials in the development of BI 811283. Secondary objectives are the collection of antitumour efficacy data and the determination of the pharmacokinetic profile of BI 811283.

Timeline

Start
2007-06
Primary completion
2011-05
Completion
2011-05

Drugs

EvaluationDrugModalityDoseRoute
Subject BI 811283 Unknown 125 mg Intravenous
Subject BI 811283 Unknown 230 mg Intravenous

Indications