drugset / Trial / NCT00756223
Phase I Study of BI 831266 in Patients With Advanced Solid Tumours
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | BI 831266 | Unknown | 32 mg | Intravenous |
| Subject | BI 831266 | Unknown | 130 mg | Intravenous |