跳至主要内容
临床试验/NCT02395913
NCT02395913已完成1 期

Compare Safety and Pharmacokinetic Properties of Surfolase Capsule(Acebrophylline 100mg) and Surfolase CR(200mg)

Hyundai Pharmaceutical Co., LTD.0 个研究点目标入组 72 人开始时间: 2013年7月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
1 期
状态
已完成
入组人数
72
主要终点
AUCt of ambroxol

研究概览

简要总结

Acebrophylline is metabolized by being separated into Ambroxol and 7-theophylline when orally administered as a salt composed of an acid-base as a compound that was synthesized by and chloride (salifying) the ambroxol to 7-theophylline. Acebrophylline is selectively applied to the bronchial or lung tissue and inhibit the activity of phospholipase bronchoalveolar shows the expectorant action to raise the surface activity of the alveolar, leukotrienes (LTs) and by suppressing the production of prostaglandins (PGs), showed potent anti-inflammatory activity, bronchial was celebrated by reducing the bronchial hyperreactivity to normal state is allowed to recuperate or extended.

It was developed to improve compliance improve pharmaceutically Surfolase capsule(Acebrophylline 100mg) that intake twice daily 100mg to Surfolase CR(Acebrophylline 200mg) that intake once daily 200mg

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Crossover
主要目的
Treatment
盲法
None

入排标准

年龄范围
20 Years 至 55 Years(Adult)
性别
Male
接受健康志愿者

入选标准

  • Healthy male subjects between the ages of 20 and 55 years, BMI >18.5, <25, inclusive
  • *Body mass index (kg/m2) = weight(kg)/height(m)2
  • Subject who don't have congenital or chronic diseases and have no abnormal medical examination results.
  • Subject is healthy (no clinically relevant findings in any of the investigations of the pre-examination) as judged by the investigator
  • Subjects who signed and dated in informed consent form indicating that the subject has decided to participate in the study after being informed of all pertinent aspects of the study

排除标准

  • Subject with known for hypersensitivity reaction to acebrophylline, xanthine and food.
  • Patients with genetic problems such as galactose intolerance, Lapp lactase deficiency or glucose-galactose malabsorption
  • Subject with serious active cardiovascular, respiratory, hepatologic, renal, hematologic, gastrointestinal, immunologic, dermal, neurologic, or psychological disease or history of such disease
  • Subject with known for history of gastrointestinal disease or gastrointestinal surgery which affect on the absorption drug
  • Subjects with any of the following condition in screening (blood pressure, 12-lead ECG, blood, urinalysis, etc.)
  • Subject with any of the following conditions in laboratory test i. AST(sGOT) or ALT(sGPT) > Upper normal limit × 1.25 ii. Total bilirubin > Upper normal limit × 1.5
  • If the estimated GFR < 80mL/min/1.76m2 using MDRD formula.
  • Systolic blood pressure <=90mmHg or diastolic blood pressure >=150mmHg or a person showing the corresponding figures <=50mmHg or >=100mmHg in vital signs.
  • Who has history of drug abuse (especially hypnotic, central acting analgesics, psychotropic drugs, such as opiates or central nervous system acting drug) or shows positive reactions to drug of abuse in urine drug screening tests.
  • Excessive caffeine and alcohol intake, smoking person(caffeine: > 5cups/day, alcohol: >210g/week, tobacco: > 10 cagarettes/day)
  • Use of any prescription medication within 14 days prior to study medication dosing or use of any medication such as over-the-counter medication including oriental medication within 7 days prior to study medication dosing
  • Participation in any clinical investigation within 60days prior to study medication dosing
  • Subjects with whole blood donation within 60days, component blood donation within 30days
  • Subjects with decision of nonparticipation through investigator's review due to laboratory test results or other excuse such as non-responding to request or instruction by investigator

研究组 & 干预措施

T3

Experimental

干预措施: Surfolase CR (200mg, T3) (Drug)

R

Active Comparator

干预措施: Surfolase capsule (100mg) (Drug)

T1

Experimental

干预措施: Surfolase CR (200mg, T1) (Drug)

T4

Experimental

干预措施: Surfolase CR (200mg, T4) (Drug)

结局指标

主要结局

AUCt of ambroxol

时间窗: blood serum sampling

Cmax of ambroxol

时间窗: blood serum sampling

次要结局

  • AUCinf of ambroxol(blood serum sampling)
  • Tmax of ambroxol(blood serum sampling)
  • t1/2 of ambroxol(blood serum sampling)

研究者

申办方类型
Industry
责任方
Sponsor

相似试验