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Study of Relative Bioavailability of Mobic Manufactured in China in Comparison With Mobic Manufactured in Germany in Chinese Healthy Volunteers

Phase 1
Completed
Conditions
Healthy
Interventions
Drug: Mobic, China, 7.5 mg
Drug: Mobic, Germany, 7.5 mg
Registration Number
NCT02183142
Lead Sponsor
Boehringer Ingelheim
Brief Summary

The objective of this study is to compare the pharmacokinetic parameters of the 7.5 mg Mobic tablet manufactured in china in comparison with 7.5 mg tablets manufactured in Germany

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
Male
Target Recruitment
20
Inclusion Criteria
  • Chinese healthy male volunteers as determined by result of screening
  • Written informed consent in accordance with Good Clinical Practice (GCP)
  • Age >= 18 and <= 40 years
  • Broca > - 20% and < + 20%
Exclusion Criteria
  • Any finding of the medical examination (blood pressure, pulse rate and Electrocardiogram (ECG) deviating from normal and of clinical relevance
  • Gastrointestinal, hepatic, renal, respiratory, cardiovascular, metabolic, immunological or hormonal disorder
  • Surgery of the gastro-intestinal tract (except appendectomy)
  • Diseases of the central nervous system (such as epilepsy) or psychiatric disorders
  • Chronic or relevant acute infections
  • Hypersensitivity to Mobic and/or non-steroidal anti-inflammatory drugs
  • Intake any drugs within 1 month before randomization
  • Participation in another trial with an investigational drug within the last 2 month or during the trial
  • Smokers ( >= 10 cigarettes or >= 3 cigars or >= 3 pipes/day) or inability to refrain from smoking on study days
  • Alcohol or drug abuse
  • Blood donation within the last 1 month
  • Excessive physical activities within the last 5 days
  • History of hemorrhagic diatheses
  • History of gastro-intestinal ulcer, perforation or bleeding
  • History of bronchial asthma

Study & Design

Study Type
INTERVENTIONAL
Study Design
CROSSOVER
Arm && Interventions
GroupInterventionDescription
Mobic GermanyMobic, China, 7.5 mg-
Mobic GermanyMobic, Germany, 7.5 mg-
Mobic ChinaMobic, China, 7.5 mg-
Mobic ChinaMobic, Germany, 7.5 mg-
Primary Outcome Measures
NameTimeMethod
Maximum measured concentration of the analyte in plasma (Cmax)Up to 96 hours after drug administration
Area under the concentration-time curve of the analyte in plasma from time zero to infinity (AUC 0-infinity)Up to 96 hours after drug administration
Secondary Outcome Measures
NameTimeMethod
Time to achieve Cmax (tmax)Up to 96 hours after drug administration
Area under the concentration-time curve of the analyte in plasma from time zero to t (AUC 0-t)Up to 96 hours after drug administration
Number of patients with clinically relevant changes from baseline in physical examination (pulse rate, systolic and diastolic blood pressure)Baseline, up to day 5 after last drug administration
Global assessment of tolerability by investigator on a 4-point scaleDay 5 after last drug administration
Terminal rate constant in plasma (λ)Up to 96 hours after drug administration
Terminal half-life of the analyte in plasma (t1/2)Up to 96 hours after drug administration
Mean residence time of the analyte (MRT)Up to 96 hours after drug administration
Apparent clearance of the analyte in plasma following extravascular administration (CL/F)Up to 96 hours after drug administration
Apparent volume of distribution following extravascular administration (Vd/F)Up to 96 hours after drug administration
Number of patients with clinically relevant changes from baseline in laboratory valuesBaseline, up to day 5 after last drug administration
Number of Participants with Adverse EventsUp to day 5 after last drug administration
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