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Spots Global Cancer Trial Database for To Determine the Maximum Tolerated Dose (MTD) of BIBF 1120 in Patients With Solid Tumours

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Trial Identification

Brief Title: To Determine the Maximum Tolerated Dose (MTD) of BIBF 1120 in Patients With Solid Tumours

Official Title: An Open Label Dose Escalation Study of BIBF 1120 Administered Orally for Four Weeks in Patients With Advanced Solid Tumours With Repeated Administration in Patients With Clinical Benefit

Study ID: NCT01951846

Interventions

BIBF 1120

Study Description

Brief Summary: The primary objective of this study was to determine the maximum tolerated dose (MTD) of BIBF 1120 in patients with solid tumours by the monitoring of drug-related adverse events. Secondary objectives were the evaluation of safety, efficacy, pharmacokinetics, and pharmacodynamics.

Detailed Description:

Keywords

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

Klinik für Tumorbiologie, Abteilung Internistische Onkologie, Freiburg, , Germany

Contact Details

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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