A Phase 2 interventional study of Adriamycin, cyclophosphamide, vindesine, valproic acid in Small Cell Lung Carcinoma, sponsored by European Lung Cancer Working Party. Completed at 5 sites in Belgium. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2015-02-12.
Sponsored by European Lung Cancer Working Party · Phase 2, Interventional, and Treatment
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.
1,203 studies on the registry are indexed under Small Cell Lung Carcinoma; 342 are open to participants now.
This study's enrollment of 64 is above the median of 56 across 1,031 interventional studies indexed under Small Cell Lung Carcinoma.
Browse Small Cell Lung Carcinoma studies →European Lung Cancer Working Party is the lead sponsor of 12 studies on the registry; 1 is open to participants now.
Counted across the registry records on this site, refreshed daily.
Exclusion Criteria:
Chemotherapy regimen (adriamycin, cyclophosphamide, vindesine) plus valproic acid
Drug: Adriamycin, cyclophosphamide, vindesine, valproic acid
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
Six-months progression-free survival
Time frame: The period between the day of registration and the date of first progression
Survival
Time frame: Survival will be dated from the date of registration
Response rate
Time frame: Every three cycles of chemotherapy
Toxicity
Time frame: After each course of chemotherapy and at the end of treatment
This study is completed, as verified in Feb 2015. You cannot join it, but the record below documents what was studied.
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European Lung Cancer Working Party