Healthy
Conditions
Brief summary
Study to investigate the relative bioavailability of concomitant administration of clopidogrel and telmisartan (Test 1) relative to the bioavailability of SR26334 alone (Reference 1), and relative to the bioavailability of telmisartan alone (Reference 2). And to investigate the bioavailability of SR26334 following administration of clopidogrel 30 minutes after intake of telmisartan (Test 2) relative to the bioavailability of SR26334 alone (Reference 1), and relative to the bioavailability of telmisartan alone (Reference 2)
Interventions
DRUGTelmisartan
DRUGClopidogrel
Sponsors
Boehringer Ingelheim
Study design
Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
40 Years to No maximum
Healthy volunteers
Yes
Inclusion criteria
* Healthy male and female subjects according to the following criteria: based upon a complete medical history, the physical examination, vital signs (BP, HR), 12-lead ECG, clinical laboratory tests * Signed and dated written informed consent prior to admission to the study in accordance with Good Clinical Practice (GCP) and local legislation * Age \>= 40 years * Body Mass Index (BMI) \>=18.5 and \<=29.9 kg/m2 * Good venous status of forearms
Exclusion criteria
* Any finding of the medical examination (including blood pressure, heart rate, and electrocardiogram) deviating from normal and of clinical relevance * Gastrointestinal, hepatic, renal, respiratory, cardiovascular, metabolic, immunologic or hormonal disorders * Surgery of gastrointestinal tract (except appendectomy) * Diseases of the central nervous system (such as epilepsy) or psychiatric disorders or neurological disorders * History of relevant orthostatic hypotension, fainting spells or blackouts * Chronic or relevant acute infections * History of an allergy/hypersensitivity (including drug allergy) which is deemed relevant to the trial as judged by the investigator * Intake of drugs with a long half-life (\> 24 hours) within at least one month or less than 10 half-lives of the respective drug prior to administration or during the trial * Use of any drugs, which might reasonably influence the results of the trial based on the knowledge at the time of protocol preparation within 10 days prior to administration or during the trial * Participation in another trial with an investigational drug within two months prior to administration or during the trial * Smoker (more than 10 cigarettes or three cigars or three pipes/day) * Alcohol abuse (more than 60 g/day) * Drug abuse * Blood donation or loss of more than 400 mL within four weeks prior to administration or during the trial. * Excessive physical activities (within five days prior to administration or during the trial) * Any laboratory value outside the reference range of clinical relevance * History of hereditary fructose intolerance * Veins unsuited for i.v. puncture on either arm (e.g. veins which are difficult to locate, access or puncture, veins with a tendency to rupture during or after puncture, etc.) * Inability to comply with the dietary regimen of study centre * Inability to comply with the investigators instructions For female subjects: * Pregnancy * Positive pregnancy test * No adequate contraception e.g. oral contraceptives, sterilization, intrauterine device (IUD) * Inability to maintain this adequate contraception during the whole study period * Lactation period
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| AUC0-∞ (area under the concentration time curve of the analyte in plasma over the time interval from 0 extrapolated to infinity) | up to 72 hours post dose |
| Cmax (maximum concentration of the analyte in plasma) | up to 72 hours post dose |
Secondary
| Measure | Time frame |
|---|---|
| Number of subjects with clinically significant findings in ECG | up to 8 days after last drug administration |
| Number of subjects with clinically significant findings in labortory test | up to 8 days after last drug administration |
| tmax (time from dosing to the maximum concentration of the analyte in plasma) | up to 72 hours post dose |
| AUC0-tz (area under the concentration-time curve of the analytes in plasma over the time interval from 0 to the time of the last quantifiable data point) | up to 72 hours post dose |
| λz (terminal rate constant in plasma) | up to 72 hours post dose |
| Number of subjects with adverse events | up to 8 days after last drug administration |
| MRTpo (mean residence time of the analytes in the body after po administration) | up to 72 hours post dose |
| CL/F (apparent clearance of the analytes in the plasma after extravascular administration) | up to 72 hours post dose |
| Vz/F (apparent volume of distribution during the terminal phase λz following an extravascular dose) | up to 72 hours post dose |
| CLR, 0-24 (renal clearance of SR26334 in plasma from the time point t1 until the time point t2) | up to 72 hours post dose |
| t1/2 (terminal half-life of the analytes in plasma) | up to 72 hours post dose |
| Number of subjects with clinically significant findings in vital signs | up to 8 days after last drug administration |
Outcome results
None listed