Sixth Affiliated Hospital of Sun Yat-sen University
Guangzhou, Guangdong, 510655, China
NCT Number: NCT01567618
This is an open-label, phase II study to evaluate the efficacy and safety of biweekly docetaxel and DeGramont regimen on unresectable gastric adenocarcinoma in the first-line therapy.
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Notify Me18 year–80 year
All sexes
Interventional
Phase 2
Guangzhou, Guangdong, 510655, China
Primary endpoint: Overall Response Rate
Secondary endpoint: Time to progression, overall survival, safety data
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Hemoglobin 90g/L WBC 3.5 x 109/L Neutrophils 1.5 x 109/L Platelets 100 x 109/L Creatinine 133 umol/L and creatinine clearance 60 mL/min
Exclusion criteria
Docetaxel 50mg/m2 iv drip, repeat every two weeks;
Efficacy will be evaluated every three cycles.
Fluorouracil 400mg/m2 iv D1; Fluorouracil 2400mg/m2 civ 46 hours; repeat fortnightly and evaluate every two cycles
Time frame: One Year
Time frame: One year
Time frame: One year
Time frame: One year
The criteria to grade the toxicity is NCI CTC 3.0
Sixth Affiliated Hospital, Sun Yat-sen University
Other
A Phase II Trial Evaluating Biweekly Docetaxel and DeGramont Regimen in First-Line Treatment of Unresectable or Metastatic Gastric Adenocarcinoma (DaeMon)
Acronym: DaeMon
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
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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