Last updated on September 2018

Initial Oral Vinorelbine Dosing Schedules in Clinical Routine in Germany and Austria

Brief description of study

The aim of this non-interventional study is to assess oral vinorelbine dose schedules (initial dose, dose increase/maintenance/reduction) applied during the initial 8 weeks of treatment under routine conditions in Germany together with the underlying reasons for the respective chosen schedules.

Clinical Study Identifier: NCT02619929

Contact Investigators or Research Sites near you

Start Over

Winicker Norimed

Kiel, Germany

Recruitment Status: Closed

Brief Description Eligibility Contact Research Team

Receive Emails About New Clinical Trials!

Sign up for our FREE service to receive email notifications when clinical trials are posted in the medical category of interest to you.