Adriamycin, cyclophosphamide, vindesine, valproic acid
DrugAdriamycin 45 mg/m² day 1 IV Cyclophosphamide 1 g/m² day 1 IV Vindesine 3 mg/m² day 1 IV Valproic acid 20-30 mg/kg/day from day -7 until the end of treatment, orally
NCT Number: NCT00759824
The primary aim of this study is to determine if the addition of valproic acid to a combination of adriamycin, cyclophosphamide and vindesine could increase progression-free survival in patients relapsing after first-line chemotherapy including platinum derivatives, cisplatin or carboplatin, and etoposide.
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Notify Me18 year and older
All sexes
Interventional
Phase 2
Department of Intensive Care Unit and Thoracic Oncology Institut Jules Bordet, Brussels, Belgium
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Adriamycin 45 mg/m² day 1 IV Cyclophosphamide 1 g/m² day 1 IV Vindesine 3 mg/m² day 1 IV Valproic acid 20-30 mg/kg/day from day -7 until the end of treatment, orally
Time frame: The period between the day of registration and the date of first progression
Time frame: Survival will be dated from the date of registration
Time frame: Every three cycles of chemotherapy
Time frame: After each course of chemotherapy and at the end of treatment
European Lung Cancer Working Party
Other
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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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