NCT00778739已完成不适用
A Two-Way Crossover, Open-Label, Single-Dose, Fed, Bioequivalence Study of Cefprozil 250 mg/5 mL Oral Suspension Versus Cefzil TM Powder for Oral Suspension (250 mg/5 mL) in Normal Healthy Non-Smoking Male and Female Subjects
适应症
干预措施
相关药物
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 32
- 试验地点
- 1
- 主要终点
- Bioequivalence
研究概览
简要总结
The study was conducted as an open-label, randomized, 2-way crossover study to compare the single-dose relative bioavailability of Cefprozil 250 mg/5 mL Oral suspension versus Cefzil TM Powder for Oral Suspension (250 mg/5 mL) following one 5 mL dose under fed conditions
详细描述
The study was designed to compare the rate and extent of absorption of cefprozil from the following products under fed condition:
- CEFPROZIL FOR ORAL SUSPENSION USP 250 mg/ 5 mL (Ranbaxy Laboratories Limited, India)
- Cefzil ® (CEFPROZIL) for oral suspension equivalent to 250mg/5mL anhydrous, cefprozil (Bristol-Myers Squibb Company USA) The bioequivalence of these formulations was assessed for cefprozil (Bristol-Myers Squibb Company, USA)
Thirty -two subjects (32) were recruited for the study of which 16 were males and 16 were females. All of them completed the study
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Crossover
- 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
- 是
入选标准
- •Non-smoking male or female with a minimum age of 18 years
- •Body Mass Index (BMI= weight/ height) greater than or equal to 18.5 kg/m3 and less than or equal to 29.9 kg/m3
- •Normal findings in physical examination, 12- lead ECG and vital signs (blood pressure between 100-140/60-90 mm Hg, heart rate between 50-90 beats/min, temperature between 35.8°C and 37.5 °C
- •Negative for drug abuse, nicotine, hepatitis B-surface antigen, hepatitis C and HIV, and for female subjects pregnancy serum (serum β-CG)
- •No clinical laboratory values outside of the acceptable range as defined by BCR, unless the Principal Investigator decided that they were not clinically significant
- •Female subjects who were surgically sterile for at least 6 months or post -menopausal for one year, or who avoided pregnancy prior to the study, during the study and up until one month after end of the study
- •Availability of the subject for the entire study period and willingness to adhere to the protocol requirements as evidenced by signed ICF
排除标准
- •Subject candidates who met the following criteria were excluded::
- •Known history of hypersensitivity to cefprozil (e.g. Cefzil TM , cephalosporin antibiotics or penicillin antibiotics
- •Known history or presence of cardiac, pulmonary, gastrointestinal, endocrine, musculoskeltal, neurological, hematological, liver or kidney disease, unless judged not clinically significant by the principal investigator or Sub-investigator.
- •Presence of any significant physical or organ abnormality
- •Any history or evidence of food allergies
- •Any subject with history of drug abuse
- •Any significant illness
- •History of colitis
- •Significant recent history of Asthma
- •Any history of severe allergic reaction
- •Any subject with recent hi story of alcohol abuse
- •Use of any prescription medication within 14 days preceding study
- •Use of OTC medication within 7 days before study
- •Female subjects: use of contraceptives (oral, transdermal, implant, Mirena ®) within 30 days prior to drug administration or a depot injection of progesterone drug (eg. Depo-Provera®) within one year prior to drug administration
- •Female subjects with evidence of pregnancy or lactation
- •Any subject with blood drawn prior to the study during the conduct of clinic study other than BCR or within lock out period specified by previous study conducted by BCR
- •Participation in clinical trial with investigational drug within 30 days preceding study
研究组 & 干预措施
1
Experimental
CEFPROZIL FOR ORAL SUSPENSION USP 250 mg/ 5 mL
干预措施: CEFPROZIL FOR ORAL SUSPENSION USP 250 mg/ 5 mL (Drug)
2
Active Comparator
CEFPROZIL FOR ORAL SUSPENSION USP 250 mg/ 5 mL
干预措施: CEFPROZIL FOR ORAL SUSPENSION USP 250 mg/ 5 mL (Drug)
结局指标
主要结局
Bioequivalence
次要结局
未报告次要终点
研究者
研究点 (1)
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