Study to Assess Safety, Tolerability and Pharmacokinetics of Single Rising Doses of BEA 2180 BR in Healthy Male Volunteers

Phase 1

Completed

• Conditions: Healthy
• Interventions: Drug: Placebo; Drug: BEA 2180 BR - rising dose

• Registration Number: NCT02254135
• Lead Sponsor: Boehringer Ingelheim

Brief Summary

Study to investigate safety, tolerability, and pharmacokinetics of single rising peroral doses of BEA 2180 BR

Detailed Description

Not available

Study Timeline

• Study Start: 2006-12
• Primary Completion: 2007-01
• Status Verified: 2014-09
• Study First Submitted: 2014-09-30
• Study First Submitted QC: 2014-09-30
• Last Update Submitted: 2014-09-30
• Study First Posted: 2014-10-01
• Last Update Posted: 2014-10-01

Recruitment & Eligibility

• Status: COMPLETED
• Sex: Male
• Target Recruitment: 24

Inclusion Criteria

1. Healthy males according to the following criteria:

   Based upon a complete medical history, including the physical examination, vital signs (BP, PR), 12-lead ECG, clinical laboratory tests

2. Age ≥21 and ≤55 years

3. BMI ≥18.5 and <30 kg/m2 (Body Mass Index)

4. Signed and dated written informed consent prior to admission to the study in accordance with Good Clinical Practice (GCP) and the local legislation

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Exclusion Criteria

1. Any finding of the medical examination (including BP, PR, and ECG measurements) deviating from normal and of clinical relevance

2. Evidence of a clinically relevant concomitant disease

3. Gastrointestinal, hepatic, renal, respiratory, cardiovascular, metabolic, immunological or hormonal disorders

4. Diseases of the central nervous system (such as epilepsy) or psychiatric disorders or neurological disorders

5. History of relevant orthostatic hypotension, fainting spells or blackouts

6. Chronic or relevant acute infections

7. History of relevant allergy/hypersensitivity (including allergy to the drug or its excipients) as judged clinically relevant by the investigator

8. Intake of drugs with a long half-life (>24 hours) within at least 1 month or less than 10 half-lives of the respective drug prior to randomisation

9. 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 enrolment in the study or during the study

10. Participation in another trial with an investigational drug within 30 days prior to randomisation

11. Smoker (>10 cigarettes or >3 cigars or >3 pipes/day)

12. Inability to refrain from smoking on trial days as judged by the investigator

13. Alcohol abuse (regularly more than 40 g alcohol per day)

14. Drug abuse

15. Blood donation (more than 100 mL blood within 4 weeks prior to randomisation or during the trial)

16. Excessive physical activities within 1 week prior to randomisation or during the trial

17. Any laboratory value outside the reference range that is of clinical relevance

18. Inability to comply with dietary regimen of the study centre

    The following exclusion criteria are specific for this study due to the known class side effect profile of anticholinergic drugs:

19. History of hypersensitivity to tiotropium and/or related drugs of these classes

20. History of narrow-angle glaucoma

21. History of prostatic hyperplasia

22. History of bladder-neck obstruction

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Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Placebo	Placebo	-
BEA 2180 BR solution - rising dose	BEA 2180 BR - rising dose	-

Primary Outcome Measures

Name	Time	Method
Number of subjects with abnormal findings in physical examination	up to 14 days after last procedure
Number of subjects with clinically significant changes in vital signs	up to 14 days after last procedure	(Blood pressure (BP), pulse rate (PR), respiration rate (RR), oral body temperature)
Number of subjects with clinically significant changes in 12-lead electrocardiogram (ECG)	up to 14 days after last procedure
Number of subjects with abnormal changes in laboratory parameters	up to 14 days after last procedure
Number of subjects with adverse events	up to 14 days after last procedure
Assessment of tolerability by the investigator on a 4-point scale	14 days after last procedure

Secondary Outcome Measures

Name	Time	Method
AUC0-∞ (area under the concentration-time curve of the analyte in plasma over the time interval from 0 extrapolated to infinity)	up to 48 h after drug administration
%AUCtz-∞ (the percentage of the AUC0-∞ that is obtained by extrapolation)	up to 48 h after drug administration
Cmax (maximum measured concentration of the analyte in plasma)	up to 48 h after drug administration
tmax (time from dosing to maximum measured concentration of the analyte in plasma)	up to 48 h after drug administration
AUC0-tz (area under the concentration-time curve of the analyte in plasma over the time interval from 0 to the time of the last quantifiable data point)	up to 48 h after drug administration
λz (terminal rate constant in plasma)	up to 48 h after drug administration
t1/2 (terminal half-life of the analyte in plasma)	up to 48 h after drug administration
MRTpo (mean residence time of the analyte in the body after peroral administration)	up to 48 h after drug administration
CL/F (clearance of the analyte in plasma after peroral administration)	up to 48 h after drug administration
Vz/F (apparent volume of distribution during the terminal phase λz following a peroral dose)	up to 48 h after drug administration
Aet1-t2 (amount of analyte eliminated in urine from the time point t1 to time point t2)	up to 48 h after drug administration
fet1-t2 (fraction of analyte eliminated in urine from time point t1 to time point t2)	up to 48 h after drug administration
CLR,t1-t2 (renal clearance of the analyte from the time point t1 until the time point t2)	up to 48 h after drug administration