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Safety, Tolerability, Pharmacodynamics and Pharmacokinetics of BI 653048 BS H3PO4 Capsule Assessing Endotoxin-induced Inflammatory Response in Healthy Male Subjects

Phase 1
Completed
Conditions
Healthy
Interventions
Drug: Placebo
Drug: BI 653048 BS
Drug: endotoxin escherichia coli (E. coli) lipopolysaccharide (LPS)
Registration Number
NCT02224105
Lead Sponsor
Boehringer Ingelheim
Brief Summary

The general aim of the current study was to investigate the safety and tolerability, and pharmacodynamics (endotoxin-induced inflammatory response of a single intravenous bolus administration of 2 ng/kg body weight Escherichia coli lipopolysaccharide (LPS)) of BI 653048 BS H3PO4 capsules in healthy male subjects following oral administration of multiple rising doses of 25 mg to 200 mg over three days compared to the active comparator prednisolone and placebo.

Pharmacodynamics were assessed by investigating the influence of LPS administration on inflammatory parameters. More specifically, it was evaluated whether and to what extent the symptoms induced by LPS challenge can be attenuated by ascending BI 653048 BS H3PO4 doses using prednisolone as positive control and placebo as negative control. A secondary objective was the exploration of pharmacokinetics of BI 653048 BS, the investigation of other pharmacodynamic parameters (biomarker) and of the tolerability of LPS.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
Male
Target Recruitment
56
Inclusion Criteria
  1. Healthy males according to the following criteria:

    Based upon a complete medical history, including the physical examination, vital signs (blood pressure, pulse rate and body temperature), 12-lead ECG, clinical laboratory tests

  2. Age ≥18 and Age ≤50 years

  3. Body mass index (BMI) ≥18.5 and BMI ≤29.9 kg/m2

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

Exclusion Criteria
  1. Any finding of the medical examination (including blood pressure, pulse rate, orthostatic test, body temperature and ECG) deviating from normal and of clinical relevance
  2. Any evidence of a clinically relevant concomitant disease
  3. Gastrointestinal, hepatic, renal, respiratory, cardiovascular, metabolic, immunological or hormonal disorders
  4. Surgery of the gastrointestinal tract (except appendectomy)
  5. Diseases of the central nervous system (such as epilepsy) or psychiatric disorders or neurological disorders
  6. History of relevant orthostatic hypotension, fainting spells or blackouts
  7. Chronic or relevant acute infections
  8. History of relevant allergy/hypersensitivity (including allergy to drug or its excipients)
  9. 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
  10. 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
  11. Participation in another trial with an investigational drug within 30 days prior to administration or during the trial
  12. Smoker (>10 cigarettes or >3 cigars or >3 pipes/day)
  13. Inability to refrain from smoking for 1 day prior to first drug administration until discharge from the study site
  14. Alcohol abuse (more than 60 g/day)
  15. Drug abuse
  16. Blood donation (more than 100 mL within four weeks prior to administration or during the trial)
  17. Excessive physical activities (within one week prior to administration or during the trial)
  18. Any laboratory value outside the reference range that is of clinical relevance
  19. Inability to comply with dietary regimen of trial site

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Prednisolone highPrednisolone high-
PlaceboPlacebo-
Prednisolone lowsodium chloride infusion-
Prednisolone highsodium chloride infusion-
Prednisolone highendotoxin escherichia coli (E. coli) lipopolysaccharide (LPS)-
Placebosodium chloride infusion-
BI 653048 BSBI 653048 BSescalating doses
BI 653048 BSendotoxin escherichia coli (E. coli) lipopolysaccharide (LPS)escalating doses
Prednisolone lowPrednisolone low-
BI 653048 BSsodium chloride infusionescalating doses
Prednisolone lowendotoxin escherichia coli (E. coli) lipopolysaccharide (LPS)-
Placeboendotoxin escherichia coli (E. coli) lipopolysaccharide (LPS)-
Primary Outcome Measures
NameTimeMethod
Assessment of tolerability by investigator on a 4-point scaleup to day 15
Maximum measured concentration of the biomarker level in plasma (Emax)up to 96 hours after first drug administration
Number of subjects with adverse eventsup to 37 days
Number of subjects with clinically significant findings in vital signsup to day 15

blood pressure, pulse rate and body temperature

Number of subjects with clinically significant findings in 12-lead electrocardiogram (ECG)up to day 15
Number of subjects with clinically significant findings in laboratory testsup to day 15
Area under the concentration-time curve of the biomarker in plasma over the time interval from 0 to the last measurable time point of the dose (AUEC)up to 96 hours after first drug administration
Secondary Outcome Measures
NameTimeMethod
Apparent clearance of the analyte in plasma following extravascular administration at steady state (CL/Fss)up to 96 hours after first drug administration
Terminal phase elimination half life at steady state (t1/2,ss)up to 96 hours after first drug administration
Mean residence time of the analyte in the body after oral administration at steady state (MRTpo,ss)up to 96 hours after first drug administration
Apparent volume of distribution during the terminal phase λz following an extravascular dose at steady state (Vz/Fss)up to 96 hours after first drug administration
Maximum measured concentration of the analyte in plasma at steady state (Cmax,ss)up to 96 hours after first drug administration
Time from dosing to maximum measured concentration of the analyte at steady state (tmax,ss)up to 96 hours after first drug administration
Area under the concentration-time curve of the analyte in the plasma over the time interval from 0 to the last measurable time point of the dose at steady state (AUC0-tz,ss)up to 96 hours after first drug administration
Area under the concentration-time curve of the analyte in plasma over the time interval from 0 extrapolated to infinity at steady state (AUC0-∞,ss)up to 96 hours after first drug administration
Percentage of the AUC0-∞ that is obtained by extrapolation at steady state (%AUCtz-∞,ss)up to 96 hours after first drug administration
Terminal phase elimination rate constant at steady state (λz,ss)up to 96 hours after first drug administration
Minimum measured concentration of the biomarker during the treatment interval (Emin)up to 96 hours after first drug administration
Area under the concentration-time curve of the biomarker in serum over the time interval from 0 to the last measurable time point of the dose (AUEC)up to 96 hours after first drug administration
Measured concentration of the biomarker at time t after the beginning of the treatment interval (Et)up to 96 hours after first drug administration
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