HealthyPhase 1NCT02273427
Effect of Different Food Compositions on Bioavailability of BIIL 284 BS in Healthy Male Volunteers
A Phase 1 study testing BIIL 284 BS, high fat meal and low fat meal in people with Healthy, run by Boehringer Ingelheim.
Trial summary
food effect, relative bioavailability, pharmacokinetics, safety and tolerability Read more about this study
- Who is it for?
- Ages 21 to 50 years, men onlyHealthy volunteers can take part
- Conditions the study is for
- Healthy
- What is being tested?
- BIIL 284 BS, high fat meal and low fat meal
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 24 participants
- Where
- No sites listed yet
- Study dates
- Feb 2000to Mar 2000
- Phase
- Phase 1
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 21 to 50 years
- Men only
- Healthy volunteers accepted
- Adult
Who may be able to join
- All participants in the study should be healthy caucasian males as determined by the results of screening, range from 21 to 50 years of age and be within +- 20% of their normal weight (Broca-Index)
- All volunteers will have given their written informed consent in accordance with Good Clinical Practice and local legislation prior to admission to the study
Who cannot join
- Any finding of the medical examination (including blood pressure, pulse rate and ECG) deviating from normal and of clinical relevance
- Gastrointestinal, hepatic, renal, respiratory, cardiovascular, metabolic, immunological or hormonal disorders
- Diseases of the central nervous system (such as epilepsy) or psychiatric disorders or neurological disorders
- History of orthostatic hypotension, fainting spells or blackouts
- Chronic or relevant acute infections
- History of allergy/hypersensitivity (including drug allergy) which is deemed relevant to the trial as judged by the investigator
Show all 16Show fewer
- Intake of drugs with a long half-life (> 24 hours) within at least one month or less than ten half-lives of the respective drug before enrolment in the study
- Use of any drugs which might influence the results of the trial (<= one week prior to administration or during the trial)
- Participation in another trial with an investigational drug (<= 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 (> 60 g/day)
- Drug abuse
- Blood donation (>= 100 ml within four weeks prior to administration or during the trial)
- Excessive physical activities (within the last week before the study)
- Any laboratory value outside the reference range of clinical relevance
About this study
Official title: Randomised 3-way Cross-over Phase I Study to Investigate the Effect of Different Food Compositions (Low Fat and High Fat Meal) on Bioavailability of BIIL 284 BS 75 mg Tablet in Healthy Male Volunteers
food effect, relative bioavailability, pharmacokinetics, safety and tolerability
- Conditions
- Healthy
- Being tested
- BIIL 284 BS, high fat meal, low fat meal
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
BIIL 284 BSDrug
high fat mealOther
low fat mealOther
| Study group | Role | What they receive |
|---|---|---|
| BIIL 284 BS fasted | Active comparator | Not described Receives: Drug: BIIL 284 BS |
| BIIL 284 BS with high fat meal | Experimental | Not described Receives: Drug: BIIL 284 BS; Other: high fat meal |
| BIIL 284 BS with low fat meal | Experimental | Not described Receives: Drug: BIIL 284 BS; Other: low fat meal |
What is being measured
The primary outcome is the main question the study is designed to answer.
Maximum concentration (Cmax)
Measured: up to 72 hours after drug administration
Area under the concentration time curve from timepoint zero extrapolated to infinity (AUC-infinity)
Measured: up to 72 hours after drug administration
Secondary outcomes (9)
Time to Cmax (tmax)
Measured: up to 72 hours after drug administration
Area under the concentration time curve from timepoint zero to time of last data point above limit of quantification (AUC-tz)
Measured: up to 72 hours after drug administration
Terminal half-life (t1/2)
Measured: up to 72 hours after drug administration
Total mean residence time (MRTtot)
Measured: up to 72 hours after drug administration
Volume of distribution during terminal phase after oral administration (Vz/F)
Measured: up to 72 hours after drug administration
Total clearance after oral administration (CLtot/F)
Measured: up to 72 hours after drug administration
Number of subjects with adverse events
Measured: up to 8 days after last drug administration
Number of subjects with clinically significant findings in vital functions
blood pressure, pulse rate, ECG
Measured: up to 8 days after last drug administration
Number of subjects with clinically significant findings in laboratory tests
Measured: up to 8 days after last drug administration
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted24 Oct 2014 (estimated)
- Study startFeb 2000
- Primary completionMar 2000
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for HealthyStudies of the same condition, open and under way.
- More trials run by Boehringer IngelheimThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase 1
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Crossover
- Masking
- None (open label)
- Enrolment
- 24 participants (actual)
Sponsor and investigators
- Lead sponsor
- Boehringer Ingelheim
- Sponsor type
- Industry (pharma, biotech, devices)
- Responsible party
- Sponsor
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT02273427
- Sponsor's protocol ID
- 543.5
- Status last verified
- Oct 2014
- First submitted
- 23 Oct 2014
- Last updated
- 24 Oct 2014
- Results posted
- No
Study at a glance
From the registry record, last updated by the sponsor on 24 Oct 2014. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Randomised 3-way Cross-over Phase I Study to Investigate the Effect of Different Food Compositions (Low Fat and High Fat Meal) on Bioavailability of BIIL 284 BS 75 mg Tablet in Healthy Male Volunteers
- ClinicalTrials.gov ID
- NCT02273427
- Acronym / sponsor ID
- 543.5
- Conditions
- Healthy
- Phase
- Phase 1
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 24 participants (actual)
- Lead sponsor
- Boehringer IngelheimIndustry (pharma, biotech, devices)
- Study start
- Feb 2000
- Primary completion
- Mar 2000 (actual)
- First posted
- 24 Oct 2014 (estimated)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
food effect, relative bioavailability, pharmacokinetics, safety and tolerability
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Crossover
- Masking
- None (open label)
- Number of arms
- 3
| Arm | Type | Receives |
|---|---|---|
| BIIL 284 BS fasted | Active comparator | Drug: BIIL 284 BS |
| BIIL 284 BS with high fat meal | Experimental | Drug: BIIL 284 BS, Other: high fat meal |
| BIIL 284 BS with low fat meal | Experimental | Drug: BIIL 284 BS, Other: low fat meal |
Who may qualify
- Ages
- 21 to 50 years
- Sex
- Male only
- Healthy volunteers
- Accepted
- Age groups
- Adult
Key inclusion criteria (2 listed)
- All participants in the study should be healthy caucasian males as determined by the results of screening, range from 21 to 50 years of age and be within +- 20% of their normal weight (Broca-Index)
- All volunteers will have given their written informed consent in accordance with Good Clinical Practice and local legislation prior to admission to the study
Key exclusion criteria (16 listed)
- Any finding of the medical examination (including blood pressure, pulse rate and ECG) deviating from normal and of clinical relevance
- Gastrointestinal, hepatic, renal, respiratory, cardiovascular, metabolic, immunological or hormonal disorders
- Diseases of the central nervous system (such as epilepsy) or psychiatric disorders or neurological disorders
- History of orthostatic hypotension, fainting spells or blackouts
- Chronic or relevant acute infections
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| BIIL 284 BS | Drug | BIIL 284 BS fasted, BIIL 284 BS with high fat meal, BIIL 284 BS with low fat meal |
| high fat meal | Other | BIIL 284 BS with high fat meal |
| low fat meal | Other | BIIL 284 BS with low fat meal |
Primary outcome
Maximum concentration (Cmax)
Time frame: up to 72 hours after drug administration
Area under the concentration time curve from timepoint zero extrapolated to infinity (AUC-infinity)
Time frame: up to 72 hours after drug administration
9 secondary outcomes
Time to Cmax (tmax)
Time frame: up to 72 hours after drug administration
Area under the concentration time curve from timepoint zero to time of last data point above limit of quantification (AUC-tz)
Time frame: up to 72 hours after drug administration
Terminal half-life (t1/2)
Time frame: up to 72 hours after drug administration
Total mean residence time (MRTtot)
Time frame: up to 72 hours after drug administration
Volume of distribution during terminal phase after oral administration (Vz/F)
Time frame: up to 72 hours after drug administration
Total clearance after oral administration (CLtot/F)
Time frame: up to 72 hours after drug administration
Number of subjects with adverse events
Time frame: up to 8 days after last drug administration
Number of subjects with clinically significant findings in vital functions
Time frame: up to 8 days after last drug administration
Number of subjects with clinically significant findings in laboratory tests
Time frame: up to 8 days after last drug administration
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 24 Oct 2014.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
The record lists no contact. Use the official record to reach the sponsor.
Questions about this trial
What is this clinical trial studying?
A Phase 1 study testing BIIL 284 BS, high fat meal and low fat meal in people with Healthy, run by Boehringer Ingelheim.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 2 inclusion and 16 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: finished, as of the sponsor's last update on 24 Oct 2014. Status can change between updates, so confirm with the study contact before making plans.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
What does this phase mean?
Phase 1 studies test a treatment in a small group of people for the first time or in a new way, mainly to check safety and find the right dose.
Not every study follows the same path, and some studies (observational studies, device studies) have no phase.
Are results available for this study?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Maximum concentration (Cmax) (time frame: up to 72 hours after drug administration). The study lists 2 primary outcomes in all. It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 24 Oct 2014.