Healthy
Conditions
Brief summary
To demonstrate that tipranavir (TPV) co-administered with ritonavir (RTV) does not affect the QT interval more than placebo co-administered with ritonavir
Interventions
Sponsors
Boehringer Ingelheim
Study design
Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
TREATMENT
Masking
DOUBLE
Eligibility
Sex/Gender
ALL
Age
18 Years to 55 Years
Healthy volunteers
Yes
Inclusion criteria
1. Healthy female and male volunteers as determined by the results of screening according to the following criteria: Based upon a complete medical history, including the physical examination, vital signs (BP, HR), 12-lead ECG, clinical laboratory tests 2. Age ≥ 18 and Age ≤ 55 years 3. BMI ≥ 18.5 and BMI ≤ 29.9 kg/m2 (Body Mass Index) 4. Signed and dated written informed consent prior to admission to the study in accordance with GCP and the local legislation
Exclusion criteria
1. Gastrointestinal, hepatic, renal, respiratory, cardiovascular, metabolic, immunological or hormonal disorders 2. Gastrointestinal tract surgery (except appendectomy) 3. Diseases of the central nervous system (such as epilepsy, seizures) or psychiatric disorders or neurological disorders 4. History of relevant orthostatic hypotension, fainting spells or blackouts. 5. Relevant acute, chronic or active chronic infections (e.g. hepatitis, HIV). 6. History of allergy/hypersensitivity (including drug allergies) that are deemed relevant to the trial as judged by the investigator 7. 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 8. Use of 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 9. Participation in another trial with an investigational drug within two months prior to administration or during the trial 10. Smoker (more than 10 cigarettes/day or 3 cigars/day or 3 pipes/day) 11. Inability to refrain from smoking on trial days 12. Alcohol abuse (more than 60 g/day) 13. Drug abuse 14. 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) 15. Blood donation (more than 100 mL within four weeks prior to administration or during the trial) 16. History of any bleeding disorder or acute blood coagulation defect 17. Hypersensitivity to ritonavir, moxifloxacin and/or related drugs of these classes 18. History of Glucose-6-phosphate-deficiency 19. Excessive physical activities (within one week prior to trial or during the trial) 20. Any laboratory value outside the reference range that is of clinical relevance 21. A history of additional risk factors for torsade de pointes (TdP) (e.g., heart failure, hypokalemia, family history of Long QT Syndrome) 22. Heart rate at screening of \> 80 bpm or \< 45 bpm 23. Any screening ECG value outside of the reference range of clinical relevance including, but not limited to PR interval \> 240 ms, QRS interval \> 120 ms, QTcB or QTcF \> 450 ms, or QT (uncorrected) \> 470 ms 24. Inability to comply with the dietary regimen of the study centre For female subjects: 25. Pregnancy 26. Positive pregnancy test 27. No adequate contraception (adequate contraception e.g. sterilisation, intrauterine pessary (IUP) or oral contraception not containing ethinyl estradiol) 28. Oral contraception containing ethinyl estradiol without the use of an additional barrier method 29. Hormone replacement containing ethinyl estradiol 30. Inability to maintain this adequate contraception during the whole study period 31. Lactation period
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Change from baseline in individually heart rate corrected QT interval length (QTcI) | baseline and 2 to 4 hours after drug administration on day3 |
Secondary
| Measure | Time frame |
|---|---|
| Change from baseline in (QTcI) | baseline and 2 to 4 hours after drug administration on day 1 |
Outcome results
None listed