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临床试验/NCT03751592
NCT03751592Unknown1 期

A Single Arm, Open-label, Multicenter, Phase Ib/IIa Studies of Chlorogenic Acid for Injection for Safety and Efficacy of Advanced Lung Cancer Patients

Sichuan J.Z. Bio-chemical Science and Technology Development Co., Ltd1 个研究点 分布在 1 个国家目标入组 144 人开始时间: 2018年7月17日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
1 期
发起方
入组人数
144
试验地点
1
主要终点
disease control rate(DCR)

研究概览

简要总结

This Ib / IIa clinical trial program focuses on the small cell lung cancer (SCLC), Squamous non-small cell lung cancer (NSCLC) and adeniform NSCLC in order to start a better development on the broad-spectrum value of chlorogenic acid: Determine the Disease control rate(DCR)of phase Ib/IIa of Chlorogenic acid for injection in the advanced Lung Cancer Patients.

详细描述

  1. Determine the Disease control rate(DCR)of Chlorogenic acid for injection in the advanced Lung Cancer Patients;
  2. Determine the Overall Survival(OS)of Chlorogenic acid for injection in the advanced Lung Cancer Patients;
  3. Determine the Objective response rate(ORR)of Chlorogenic acid for injection in the advanced Lung Cancer Patients;
  4. Determine the Progression Free Survival(PFS)of Chlorogenic acid for injection in the advanced Lung Cancer Patients;
  5. Determine Eastern Cooperative Oncology Group(ECOG).

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Recurrent small cell lung cancer (SCLC), Squamous non-small cell lung cancer (NSCLC) and adeniform NSCLC;
  • Estimated lifetime ≥ 3 months;
  • Patients who have sufficient baseline organ function and whose laboratory data can meet the following criteria at the enrollment:1)PLT count≥80×10~9/L; 2)NEUT# count≥1.5×10~9/L ;3)HGB count≥90g/L;4)Total bilirubin <=1.5 times of ULN;5)ALT/AST ≤2.5 times of ULN;
  • Female patients with negative pregnant test, and male/female patients of reproductive age without pregnancy planning in the next 12 months;
  • Volunteered for the phase 1 trial and sign the informed consent without protest.

排除标准

  • Patients who suffer from other serious complication, such as uncontrollable infection, myocardial infarction within the past 6 months at the enrollment , uncontrollable hypertension ,thromboembolism and etc.;
  • Patients with brain metastases;
  • Patients with bone metastases;
  • Patients who have primary immunodeficiency;
  • Organ transplanters recipients;
  • Patients who have received the therapy of chemotherapy within 4 weeks or radical radiotherapy with in 6 weeks before enrollment;
  • Pregnant or breast-feeding women, or patients(male and female) who have pregnancy plan;
  • Patients who had received a therapy of another investigational drug within 1 month;
  • Known active hepatitis B/hepatitis C, positive HIV/ syphilis antibody;
  • Patients who have received therapy of major surgery within 6 weeks or biopsy surgery within 2 weeks before enrollment;
  • Patient who need long term treatment of cortical hormone or other immunosuppressive drugs such as visceral organ transplanters;
  • Patients who have used nitrosoureas drug or mitomycin within 6 weeks or tyrosine kinase inhibitor within 2 weeks before enrollment;
  • Patients who or have received radical radiotherapy within 6 weeks or local palliative radiotherapy within 2 weeks before enrollment;
  • History of drug abuse;
  • Patients who was treated with Immunologic drugs in 3 months;
  • Other patients judged ineligible for enrollment in the study by the investigator (sub-investigator).

研究组 & 干预措施

Chlorogenic acid, Treatment, powder

Experimental

Chlorogenic acid for injection(30mg/bottle) is white or off-white freeze-dried lump or powder,it can be easily dissolved in water, which solubility is 20%.

干预措施: Chlorogenic acid (Drug)

结局指标

主要结局

disease control rate(DCR)

时间窗: Within the first 10 weeks after the first dose of chlorogenic acid for injection

次要结局

  • objective response rate (ORR)(Within the first 10 weeks after the first dose of chlorogenic acid for injection)
  • progress free survival(PFS)(Within the first 10 weeks after the first dose of chlorogenic acid for injection)
  • Overall Survival(OS)(Within the first 10 weeks after the first dose of chlorogenic acid for injection)
  • Eastern Cooperative Oncology Group (ECOG) score standard(Within the first 10 weeks after the first dose of chlorogenic acid for injection)

研究者

发起方
Sichuan J.Z. Bio-chemical Science and Technology Development Co., Ltd
申办方类型
Industry
责任方
Sponsor

研究点 (1)

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