- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02215031
Safety, Tolerability and Pharmacokinetics of Single Rising Intravenous Doses of BI 44370 BS Solution in Healthy Male Volunteers
August 12, 2014 updated by: Boehringer Ingelheim
Safety, Tolerability and Pharmacokinetics of Single Rising Intravenous Doses (10 to 50 mg) of BI 44370 BS Solution in Healthy Male Volunteers (Randomised, Single-blind, Placebo-controlled Within Dose Groups, Phase I)
Study to investigate safety, tolerability, and pharmacokinetics of BI 44370 BS solution for intravenous (i.v.) infusion
Study Overview
Study Type
Interventional
Enrollment (Actual)
23
Phase
- Phase 1
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
21 years to 50 years (Adult)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
Male
Description
Inclusion Criteria:
- Healthy males according to the following criteria based upon a complete medical history, including the physical examination, vital signs (Blood Pressure (BP), Pulse Rate (PR), Respiratory Rate (RR) and body temperature), 12-lead ECG, clinical laboratory tests
- Age 21 to 50 years inclusive
- Body Mass Index (BMI) 18.5 to 29.9 kg/m2 inclusive
- Signed and dated written informed consent prior to admission to the study in accordance with Good Clinical Practice and German law
Exclusion Criteria:
- Any finding of the medical examination (including BP, PR, RR, body temperature and ECG) deviating from normal and of clinical relevance
- Any evidence of a clinically relevant concomitant disease
- Gastrointestinal, hepatic, renal, respiratory, cardiovascular, metabolic, immunological or hormonal disorders
- Surgery of the 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 relevant allergy/hypersensitivity (including allergy to drug or its excipients)
- 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 drugs which might reasonably influence the results of the trial or that prolong the QT/QTc interval 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 (> 10 cigarettes or > 3 cigars or > 3 pipes/day)
- Inability to refrain from smoking on trial days
- Alcohol abuse (more than 60 g/day)
- Drug abuse
- Blood donation (more than 100 mL within four weeks prior to administration or during the trial)
- Excessive physical activities (within one week prior to administration or during the trial)
- Any laboratory value outside the reference range that is of clinical relevance
- Inability to comply with dietary regimen of trial site
- A marked baseline prolongation of QT/QTc interval (e.g., repeated demonstration of a QTc interval >450 ms)
- A history of additional risk factors for torsade de pointes (e.g., heart failure, hypokalemia, family history of Long QT Syndrome)
- Not willing to use adequate contraception (condom use plus another form of contraception, e.g. spermicide, oral contraceptive taken by female partner, sterilisation, or intrauterine device) during the whole study period from the time of the first intake of study drug until three months after the last intake
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Placebo Comparator: Placebo
|
|
Experimental: BI 44370
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
Number of patients with clinically significant findings in vital signs
Time Frame: up to 16 days
|
up to 16 days
|
Number of patients with clinically significant findings in 12-lead electrocardiogram (ECG)
Time Frame: up to 16 days
|
up to 16 days
|
Number of patients with clinically significant laboratory findings
Time Frame: up to 16 days
|
up to 16 days
|
Number of patients with adverse events
Time Frame: up to 37 days
|
up to 37 days
|
Assessment of global tolerability by investigator on a 4-point scale
Time Frame: within 14 days after last trial procedure
|
within 14 days after last trial procedure
|
Secondary Outcome Measures
Outcome Measure |
Time Frame |
---|---|
AUC0-∞ (area under the concentration-time curve of the analyte in plasma over the time interval from 0 extrapolated to infinity)
Time Frame: up to 24 hours after drug administration
|
up to 24 hours after drug administration
|
Cmax (maximum measured concentration of the analyte in plasma)
Time Frame: up to 24 hours after drug administration
|
up to 24 hours after drug administration
|
tmax (time from dosing to maximum measured concentration)
Time Frame: up to 24 hours after drug administration
|
up to 24 hours after drug administration
|
λz (terminal rate constant in plasma)
Time Frame: up to 24 hours after drug administration
|
up to 24 hours after drug administration
|
t1/2 (terminal half-life of the analyte in plasma)
Time Frame: up to 24 hours after drug administration
|
up to 24 hours 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)
Time Frame: up to 24 hours after drug administration
|
up to 24 hours after drug administration
|
%AUCtz-∞ (the percentage of the AUC0-∞ that is obtained by extrapolation)
Time Frame: up to 24 hours after drug administration
|
up to 24 hours after drug administration
|
CLR,t1-t2 (renal clearance of the analyte from the time point t1 until the time point t2)
Time Frame: up to 24 hours after drug administration
|
up to 24 hours after drug administration
|
AUC0-2 (area under the concentration-time curve of the analyte in plasma over the time interval from 0 to 2 hours after drug application)
Time Frame: up to 2 hours after drug administration
|
up to 2 hours after drug administration
|
AUCt1-t2 (area under the concentration-time curve of the analyte in plasma over the time interval from time point t1 to time point t2)
Time Frame: up to 24 hours after drug administration
|
up to 24 hours after drug administration
|
MRTinf (mean residence time of the analyte in the body after intravenous administration)
Time Frame: up to 24 hours after drug administration
|
up to 24 hours after drug administration
|
CL (total clearance of the analyte in plasma after intravascular administration)
Time Frame: up to 24 hours after drug administration
|
up to 24 hours after drug administration
|
Vz (apparent volume of distribution during the terminal phase λz following an intravascular dose)
Time Frame: up to 24 hours after drug administration
|
up to 24 hours after drug administration
|
Vss (apparent volume of distribution at steady state following intravascular administration)
Time Frame: up to 24 hours after drug administration
|
up to 24 hours after drug administration
|
Aet1-t2 (amount of analyte eliminated in urine from the time point t1 to time point t2)
Time Frame: up to 24 hours after drug administration
|
up to 24 hours after drug administration
|
fet1-t2 (fraction of analyte eliminated in urine from time point t1 to time point t2)
Time Frame: up to 24 hours after drug administration
|
up to 24 hours after drug administration
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
Helpful Links
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
September 1, 2008
Primary Completion (Actual)
November 1, 2008
Study Registration Dates
First Submitted
August 12, 2014
First Submitted That Met QC Criteria
August 12, 2014
First Posted (Estimate)
August 13, 2014
Study Record Updates
Last Update Posted (Estimate)
August 13, 2014
Last Update Submitted That Met QC Criteria
August 12, 2014
Last Verified
August 1, 2014
More Information
Terms related to this study
Other Study ID Numbers
- 1246.12
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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