Sanofi-Aventis Administrative Office
Istanbul, Turkey (Türkiye)
NCT Number: NCT00826852
The purpose of this study is:
* to assess the efficacy of the combination in terms of Objective (clinical and radiological) Response Rate * to assess the time to progression of the disease; assess the safety profile of the combination, and assess the survival time.
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Notify MeUp to 75 year
All sexes
Interventional
Phase 2
Istanbul, Turkey (Türkiye)
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
The above information is not intended to contain all considerations relevant to a patient's potential participation in a clinical trial.
weekly docetaxel 30mg/m2 and four weekly carboplatin AUC (Area under curve) 5
Time frame: After the 3rd cycle, 6th cycle and at every follow up visit
Time frame: At each visit
Time frame: Until the progression of all patients
Time frame: At the end of the study
Sanofi
Industry
Phase II Trial of Weekly Docetaxel and Four Weekly Carboplatin Combination in the First-line Treatment of Advanced Non-small Cell Lung Cancer
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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