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Brief Title: Phase I Study of BI 831266 in Patients With Advanced Solid Tumours
Official Title: An Open-label Phase I Single Dose Escalation Trial of Two Dosing Schedules of BI 831266 Administered Intravenously Over 24 h Continuously in Patients With Advanced Solid Tumours
Study ID: NCT00756223
Brief 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.
Detailed Description:
Minimum Age: 18 Years
Eligible Ages: ADULT, OLDER_ADULT
Sex: ALL
Healthy Volunteers: No
1257.1.4303 Boehringer Ingelheim Investigational Site, Linz, , Austria
1257.1.4302 Boehringer Ingelheim Investigational Site, Salzburg, , Austria
1257.1.4301 Boehringer Ingelheim Investigational Site, Wien, , Austria
Name: Boehringer Ingelheim
Affiliation: Boehringer Ingelheim
Role: STUDY_CHAIR