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Spots Global Cancer Trial Database for 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)

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Trial Identification

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

Study Description

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

Eligibility

Minimum Age: 71 Years

Eligible Ages: OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

Klinikum Kassel GmbH, Kassel, Hessen, Germany

LungenClinic Großhansdorf GmbH, Großhansdorf, , Germany

Thoraxklinik Universitätsklinikum Heidelberg, Heidelberg, , Germany

Klinikum der Universität München, München, , Germany

Contact Details

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

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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