Sanofi-Aventis Administrative Office
Vienna, Austria
NCT Number: NCT00432315
Primary objective:
• To assess the response rate to induction therapy with docetaxel/CDDP.
Secondary objectives:
To assess
* Resectability after induction therapy * Time to progression * Overall survival * Safety profile * Quality of Life
Looking for future studies?
Notify Me19 year–75 year
All sexes
Interventional
Phase 2
Vienna, Austria
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.
Time frame: every 3 months until tumour progression and thereafter every 6 months until death
Time frame: every 3 months until tumour progression and thereafter every 6 months until death
Time frame: every 3 months until tumour progression and thereafter every 6 months until death
Time frame: every 3 months until tumour progression and thereafter every 6 months until death
Time frame: throughout the study
Time frame: every 3 months until tumour progression and thereafter every 6 months until death
Sanofi
Industry
Multicenter Phase II Study Evaluating Docetaxel and CDDP as Induction Regimen Prior to Surgery or Radiochemotherapy With Docetaxel, Followed by Adjuvant Docetaxel Therapy in Chemonaive Patients With NSCLC Stage II, IIIa and IIIb
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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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