The following info and data is provided "as is" to help patients around the globe.
We do not endorse or review these studies in any way.
Brief Title: An Dose Escalation Trial of Oral BIBF 1120 in Combination With Intravenous Vinorelbine in Elderly Patients With Advanced Non Small Lung Cell Cancer - Stage IV (VENUS-1)
Official Title: An Open Label Phase I Dose Escalation Trial of Oral BIBF 1120 in Combination With Intravenous Vinorelbine in Elderly Patients With Advanced Non Small Lung Cell Cancer - Stage IV
Study ID: NCT01684111
Brief Summary: To investigate the maximum tolerated dose of BIBF 1120, safety and pharmacokinetics in escalating doses administered with Vinorelbine i.v. in elderly patients with advanced Non-Small Lung Cancer (Stage IV).
Detailed Description: Patients older than 70 years could be enroled in this clinical trial. The trial is being carried out in two trial centres in Germany. For the planned sample size it is assumed that two different dosage groups are needed with 6 patients on each dosage group with the option to deescalate the first dosage. Altogether this leads to an estimated sample size of maximal 18 patients. * Duration of treatment/patient: up to 6 month * Follow Up: at least 6 month
Minimum Age: 71 Years
Eligible Ages: OLDER_ADULT
Sex: ALL
Healthy Volunteers: No
Klinikum Kassel GmbH, Kassel, Hessen, Germany
LungenClinic Großhansdorf GmbH, Großhansdorf, , Germany
Thoraxklinik Universitätsklinikum Heidelberg, Heidelberg, , Germany
Klinikum der Universität München, München, , Germany
Name: Prof. Dr. Rudolf M. Huber, MD
Affiliation: Klinikum der Universität München, D-80336 München
Role: PRINCIPAL_INVESTIGATOR
Name: Prof. Dr. Martin Wolf, MD
Affiliation: Klinikum Kassel GmbH, D-34125 Kassel
Role: STUDY_CHAIR