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临床试验/KCT0003158
KCT0003158尚未招募未知

A pilot study of trastuzumab in combination with gemcitabine plus cisplatin in patients with advanced biliary tract cancer

Asan Medical Center0 个研究点目标入组 15 人开始时间: 待定最近更新:

试验速览

阶段
未知
状态
尚未招募
入组人数
15

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional Study

入排标准

年龄范围
19(Year) 至 o Limit(—)
性别
All

入选标准

  • Inclusion criteria related to disease
  • 1.The subject with disease that is not amendable to a curative treatment approach or locally advanced or metastatic or unresectable CCC(Cholangiocarcinoma) with histological diagnosis
  • 2.At least one measurable(per RECIST 1.1) lesion
  • 3.Primary or metastatic tumor with HER2 positive defined on IHC2+, FISH+ or IHC3+
  • 4.ECOG Performance status 0 or 1
  • 5.At least 3 months for life expectancy
  • Common inclusion criteria
  • 6.Men or women over 19 years at time of signing ICF(Informed Consent Form)
  • 7.Signed Informed Consent Form

排除标准

  • Exclusion criteria related to tumor
  • 8.Received prior chemotherapy for advanced/metastatic disease (the adjuvant/neoadjuvant chemotherapy completed at least 6 months before enrolled will be accepted)
  • 9.Not recovery from toxicities related to any prior treatments excluding alopecia (eg, neurological toxicity to = Grade 2)
  • 10.History of malignancy other than CCC within 5 years prior to screening, with the exception of malignancies with a negligible risk of metastasis or death, such as carcinoma in situ or thyroid papillary carcinoma
  • Hematology, chemistry or organ function
  • 11.ANC < 1.5 × 109/L, or Platelet < 100 × 109/L
  • 12.Total bilirubin > 1.5 × ULN; or AST/ ALT > 2.5 × ULN (Upper Limit of Normal or if the tumor has expanded into the liver, > 5 × ULN); or, alkaline phosphatase > 2.5 × ULN (or > 5 × if the tumor has expanded into the liver, or > 10 × ULN if the tumor has expanded into the brain without liver,); or albumin < 2.5 g/dL
  • 13.Creatinine clearance < 60 mL/min(calculated using the Cockcroft-Gault formula)
  • Other exclusion criteria related to IP(Investigational Product)
  • 14.History of proved congestive heart failure; angina with medication; evidence of transmural myocardial infarction on ECG; uncontrolled hypertension(systolic> 180 mmHg or diastolic> 100 mmHg); clinically significant heart valve disease; uncontrolled arrhythmia
  • 15.LVEF(Left Ventricular Ejection Fraction) < 50% (calculated by cardiac sonography or MUGA(MUltiGAted acquisition)
  • 16.Subject with rest dyspnea due to metastatic tumor or other disease or who needs oxygen therapy
  • 17.Chronic or high-dose corticosteroid treatment
  • 18.Clinically significant Hearing impairment
  • Common exclusion criteria
  • 19.History or evidence of CNS(Central Nervous System) metastases
  • 20.Interstitial pneumonia or pulmonary fibrosis with symptom and exact lesion on chest X-ray
  • 21.Hearing loss
  • 22.Uncontrolled significant systemic disease (eg, infection or uncontrolled DM-Diabetes Mellitus)
  • 23.Pregnant or lactating females
  • 24.Sexually active fertile subjects without contraception
  • 25.Treatment with other investigational therapy within 4 weeks prior to initiation of study treatment
  • 26.Radiotherapy within 4 weeks prior to initiation of study treatment (the rest at least 2 weeks after palliative radiotherapy for bone metastasis and recovery from the effects of radiation will be accepted.)
  • 27.Major surgery within 4 weeks prior to initiation of study treatment
  • 28.History of HIV((human immunodeficiency virus) and active HBV(Hepatitis B virus) or HCV(Hepatitis C virus)
  • 29.Previously identified allergy or hypersensitivity to components of the study treatment formulations

研究者

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