Bioequivalence of BIBR 277 Tablet (Mannitol Based) Compared With Capsule Formulation in Healthy Male Volunteers
Information source: Boehringer Ingelheim
ClinicalTrials.gov processed this data on August 23, 2015 Link to the current ClinicalTrials.gov record.
Condition(s) targeted: Healthy
Intervention: BIBR 277 tablet (Drug); BIBR 277 capsule (Drug)
Phase: Phase 1
Status: Completed
Sponsored by: Boehringer Ingelheim
Summary
Study to investigate the bioequivalence of BIBR 277 tablet (Mannitol based) vs. BIBR 277
capsule
Clinical Details
Official title: Bioequivalence Study of BIBR 277 Tablet (Mannitol Based) Compared With Its Capsule Formation in Healthy Male Volunteers
Study design: Allocation: Randomized, Intervention Model: Crossover Assignment, Masking: Open Label, Primary Purpose: Treatment
Primary outcome: Cmax (maximum observed concentration of the Telmisartan in plasma)AUC0-72hr (area under the concentration-time curve of the Telmisartan in plasma from zero time to 72hr
Secondary outcome: Individual time courses of the Telmisartan plasma concentrationstmax (time to reach Cmax) t1/2 (terminal half-life of the Telmisartan in plasma) AUC0-∞(area under the concentration-time curve of Telmisartan in plasma from zero time to infinity) MRT0-∞ (total mean residence time of Telmisartan molecules in the body) Number of subjects with adverse events Number of subjects with clinically significant findings in vital signs Number of subjects with clinically significant findings in ECG Number of subjects with clinically significant findings in laboratory tests
Eligibility
Minimum age: 20 Years.
Maximum age: 35 Years.
Gender(s): Both.
Criteria:
Inclusion Criteria:
1. Age >= 20 and <= 35 years
2. Weight: BMI > 17. 6 and < 26. 4 (Weight (kg) / Height (m)2)
3. Subjects judged by the investigator to be eligible as study subjects, with no
clinically significant findings after screening
4. Subjects who volunteer to participate and are able to fully understand and agree with
this study by written informed consent
Exclusion Criteria:
1. Gastrointestinal, hepatic, renal, respiratory, cardiovascular, metabolic,
immunological or hormonal disorders
2. Diseases of the central nervous system (such as epilepsy) or psychiatric disorders or
neurological disorders
3. Chronic or relevant acute infections
4. History of hepatic disorder (e. g., biliary cirrhosis, cholestasis)
5. History of serious renal disorder
6. History of or present bilateral renal artery stenosis or lack of unilateral kidney
accompanying arterial stenosis
7. History of or present cerebrovascular disorder
8. History of hyperkalemia
9. History of hypersensitivity to active ingredient (Telmisartan) or other angiotensin
II receptor antagonists
10. History of or present orthostatic hypotension or faint
11. Surgery of gastrointestinal tract (except appendectomy)
12. History of alcohol or drug abuse
13. Participation to another trial with an investigational drug within 4 months prior to
the trial
14. Whole blood donation more than 400 mL within 3 months prior to the trial
15. Whole blood donation more than 100 mL within 1 month prior to the trial
16. Donation of constituent of blood of more than 400 mL within 1 month prior to the
trial
17. Any medication which might influence the result of the trial within 10 days prior to
the trial
18. Excessive physical activities within 7 days prior to the trial
19. Alcohol drinking within 3 days prior to the trial
20. Inability to comply with restriction of protocol
21. Other than above, those who are judged by the investigator to be inappropriate as the
subjects of the study
Locations and Contacts
Additional Information
Starting date: July 2002
Last updated: October 9, 2014
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