The study will be a prospective open-label single-center study in previously treated patients with Non Small Cell Lung Cancer (NSCLC). Treatment efficacy and safety of the combination of Oshadi D and Oshadi R with Docetaxel will be will be evaluated. Patients will receive Docetaxel in combination with Oshadi D and Oshadi R. Patient will be evaluated throughout the study for safety and tolerance to multiple dose regimens of Oshadi D and Oshadi R. CT or MRI imaging will be performed prior to treatment initiation and at the end of every 3 Docetaxel cycles (12 weeks). In case of disease progression, dose augmentation will be considered or subsequent therapy.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
20
Anti cancer agents
Chemotheraphy
Hadassah Medical Center
Jerusalem, Israel
RECRUITINGoverall survival time
overall survival of the patient
Time frame: 12 months
Adverse events and serious adverse events occurence
Adverse events and serious adverse events occurred during the study
Time frame: One month following treatment initiation
Patient report outcome
To assess patients quality of life by QLC30 questionnaire
Time frame: 12 months
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