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临床试验/NCT03437785
NCT03437785已完成2 期

A Phase 2, Multi-center, Randomized, Double-blind, Parallel-group Trial to Evaluate the Efficacy and Safety of CKD-495 in Patients With Acute and Chronic Gastritis

Chong Kun Dang Pharmaceutical16 个研究点 分布在 1 个国家目标入组 250 人开始时间: 2018年1月16日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
状态
已完成
入组人数
250
试验地点
16
主要终点
Improvement rate of gastric erosion

研究概览

简要总结

To Evaluate the Efficacy and Safety of CKD-495

详细描述

A Phase 2, Multi-center, Randomized, Double-blind, Parallel-group Trial to Evaluate the Efficacy and Safety of CKD-495 in Patients with Acute and Chronic Gastritis

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Double (Participant, Investigator)

入排标准

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

入选标准

  • Male or Female subjects aged ≥ 19
  • Acute or Chronic gastritis patients who have more than 1 erosion on endoscopy within 7days prior to the use of the Investigator's Product taken date
  • Patients who have more than 1 subjective symptom

排除标准

  • Patients with peptic ulcer, gastroesophageal reflux disease, malignant tumor in the digestive system or coagulation disorder, or taking antithrombotic medicine
  • Patients who have been taken any gastritis medicine that could affect the treatment: H2 receptor antagonist, PPI(Proton Pump Inhibitor), antacid, improvement of movement in digestive system, Prostaglandin, and protective agent for gastritis
  • Patients who have to take medicine that could cause gastritis

研究组 & 干预措施

Experimental Group 1

Experimental

Patients assigned to this group are treated with CKD-495 75mg Tab.,and other 3 Placebo Tab.(Placebo of the CKD-495 150mg, ,Placebo of Artemisia Herb 95% Ethanol Soft Ext.(20→1) 60mg Tab., Placebo of the Rebamipide 100mg Tab.)

干预措施: CKD-495 75mg (Drug)

Experimental Group 1

Experimental

Patients assigned to this group are treated with CKD-495 75mg Tab.,and other 3 Placebo Tab.(Placebo of the CKD-495 150mg, ,Placebo of Artemisia Herb 95% Ethanol Soft Ext.(20→1) 60mg Tab., Placebo of the Rebamipide 100mg Tab.)

干预措施: Placebo of the CKD-495 150mg (Drug)

Experimental Group 1

Experimental

Patients assigned to this group are treated with CKD-495 75mg Tab.,and other 3 Placebo Tab.(Placebo of the CKD-495 150mg, ,Placebo of Artemisia Herb 95% Ethanol Soft Ext.(20→1) 60mg Tab., Placebo of the Rebamipide 100mg Tab.)

干预措施: Placebo of Artemisia Herb 95% Ethanol Soft Ext.(20→1) 60mg (Drug)

Experimental Group 1

Experimental

Patients assigned to this group are treated with CKD-495 75mg Tab.,and other 3 Placebo Tab.(Placebo of the CKD-495 150mg, ,Placebo of Artemisia Herb 95% Ethanol Soft Ext.(20→1) 60mg Tab., Placebo of the Rebamipide 100mg Tab.)

干预措施: Placebo of the Rebamipide 100mg (Drug)

Experimental Group 2

Experimental

Patients assigned to this group are treated with CKD-495 150mg Tab.,and other 3 Placebo Tab.(Placebo of the CKD-495 75mg, Placebo of Artemisia Herb 95% Ethanol Soft Ext.(20→1) 60mg Tab., Placebo of the Rebamipide 100mg Tab.)

干预措施: CKD-495 150mg (Drug)

Experimental Group 2

Experimental

Patients assigned to this group are treated with CKD-495 150mg Tab.,and other 3 Placebo Tab.(Placebo of the CKD-495 75mg, Placebo of Artemisia Herb 95% Ethanol Soft Ext.(20→1) 60mg Tab., Placebo of the Rebamipide 100mg Tab.)

干预措施: Placebo of the CKD-495 75mg (Drug)

Experimental Group 2

Experimental

Patients assigned to this group are treated with CKD-495 150mg Tab.,and other 3 Placebo Tab.(Placebo of the CKD-495 75mg, Placebo of Artemisia Herb 95% Ethanol Soft Ext.(20→1) 60mg Tab., Placebo of the Rebamipide 100mg Tab.)

干预措施: Placebo of Artemisia Herb 95% Ethanol Soft Ext.(20→1) 60mg (Drug)

Experimental Group 2

Experimental

Patients assigned to this group are treated with CKD-495 150mg Tab.,and other 3 Placebo Tab.(Placebo of the CKD-495 75mg, Placebo of Artemisia Herb 95% Ethanol Soft Ext.(20→1) 60mg Tab., Placebo of the Rebamipide 100mg Tab.)

干预措施: Placebo of the Rebamipide 100mg (Drug)

Placebo Group

Placebo Comparator

Patients assigned to this group are treated with 4 Placebo Tab.(Placebo of the CKD-495 75mg, Placebo of the CKD-495 150mg, Placebo of Artemisia Herb 95% Ethanol Soft Ext.(20→1) 60mg Tab., Placebo of the Rebamipide 100mg Tab.)

干预措施: Placebo of the CKD-495 75mg (Drug)

Placebo Group

Placebo Comparator

Patients assigned to this group are treated with 4 Placebo Tab.(Placebo of the CKD-495 75mg, Placebo of the CKD-495 150mg, Placebo of Artemisia Herb 95% Ethanol Soft Ext.(20→1) 60mg Tab., Placebo of the Rebamipide 100mg Tab.)

干预措施: Placebo of the CKD-495 150mg (Drug)

Placebo Group

Placebo Comparator

Patients assigned to this group are treated with 4 Placebo Tab.(Placebo of the CKD-495 75mg, Placebo of the CKD-495 150mg, Placebo of Artemisia Herb 95% Ethanol Soft Ext.(20→1) 60mg Tab., Placebo of the Rebamipide 100mg Tab.)

干预措施: Placebo of Artemisia Herb 95% Ethanol Soft Ext.(20→1) 60mg (Drug)

Placebo Group

Placebo Comparator

Patients assigned to this group are treated with 4 Placebo Tab.(Placebo of the CKD-495 75mg, Placebo of the CKD-495 150mg, Placebo of Artemisia Herb 95% Ethanol Soft Ext.(20→1) 60mg Tab., Placebo of the Rebamipide 100mg Tab.)

干预措施: Placebo of the Rebamipide 100mg (Drug)

Active comparator Group 1

Active Comparator

Patients assigned to this group are treated with Artemisiae argyi folium 95% ethanol ext.(20→1) 60mg Tab, and other 3 Placebo Tab.(Placebo of the CKD-495 75mg, Placebo of the CKD-495 150mg, Placebo of the Rebamipide 100mg Tab.)

干预措施: Artemisiae argyi folium 95% ethanol ext.(20→1) 60mg (Drug)

Active comparator Group 1

Active Comparator

Patients assigned to this group are treated with Artemisiae argyi folium 95% ethanol ext.(20→1) 60mg Tab, and other 3 Placebo Tab.(Placebo of the CKD-495 75mg, Placebo of the CKD-495 150mg, Placebo of the Rebamipide 100mg Tab.)

干预措施: Placebo of the CKD-495 75mg (Drug)

Active comparator Group 1

Active Comparator

Patients assigned to this group are treated with Artemisiae argyi folium 95% ethanol ext.(20→1) 60mg Tab, and other 3 Placebo Tab.(Placebo of the CKD-495 75mg, Placebo of the CKD-495 150mg, Placebo of the Rebamipide 100mg Tab.)

干预措施: Placebo of the CKD-495 150mg (Drug)

Active comparator Group 1

Active Comparator

Patients assigned to this group are treated with Artemisiae argyi folium 95% ethanol ext.(20→1) 60mg Tab, and other 3 Placebo Tab.(Placebo of the CKD-495 75mg, Placebo of the CKD-495 150mg, Placebo of the Rebamipide 100mg Tab.)

干预措施: Placebo of the Rebamipide 100mg (Drug)

Active comparator Group 2

Active Comparator

Patients assigned to this group are treated with Rebamipide 100mg Tab.,and other 3 Placebo Tab.(Placebo of the CKD-495 75mg, Placebo of the CKD-495 150mg, Placebo of Artemisia Herb 95% Ethanol Soft Ext.(20→1) 60mg Tab.)

干预措施: Rebamipide 100mg (Drug)

Active comparator Group 2

Active Comparator

Patients assigned to this group are treated with Rebamipide 100mg Tab.,and other 3 Placebo Tab.(Placebo of the CKD-495 75mg, Placebo of the CKD-495 150mg, Placebo of Artemisia Herb 95% Ethanol Soft Ext.(20→1) 60mg Tab.)

干预措施: Placebo of the CKD-495 75mg (Drug)

Active comparator Group 2

Active Comparator

Patients assigned to this group are treated with Rebamipide 100mg Tab.,and other 3 Placebo Tab.(Placebo of the CKD-495 75mg, Placebo of the CKD-495 150mg, Placebo of Artemisia Herb 95% Ethanol Soft Ext.(20→1) 60mg Tab.)

干预措施: Placebo of the CKD-495 150mg (Drug)

Active comparator Group 2

Active Comparator

Patients assigned to this group are treated with Rebamipide 100mg Tab.,and other 3 Placebo Tab.(Placebo of the CKD-495 75mg, Placebo of the CKD-495 150mg, Placebo of Artemisia Herb 95% Ethanol Soft Ext.(20→1) 60mg Tab.)

干预措施: Placebo of Artemisia Herb 95% Ethanol Soft Ext.(20→1) 60mg (Drug)

结局指标

主要结局

Improvement rate of gastric erosion

时间窗: 14days after drug administrations

50% decreased on erosive grade

次要结局

  • cure rate of gastric erosion(14days after drug administrations)
  • Improvement rate of symptoms(14days after drug administrations)
  • Improvement rate of gastric edema(14days after drug administrations)
  • Improvement rate of gastric erythema(14days after drug administrations)
  • Improvement rate of gastric hemorrhage(14days after drug administrations)

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (16)

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