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Safety, Tolerability and Pharmacokinetics of the Fixed Dose Combination of BI 1744 CL Plus BI 54903 XX Via Respimat® B Versus the Mono Products of BI 1744 CL Via Respimat® A and BI 54903 XX Via Respimat® B in Healthy Male and Female Volunteers

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ClinicalTrials.gov Identifier: NCT02222428
Recruitment Status : Completed
First Posted : August 21, 2014
Last Update Posted : August 21, 2014
Sponsor:
Information provided by (Responsible Party):
Boehringer Ingelheim

Brief Summary:
The primary objective of this study was to compare the systemic exposure of BI 1744 BS and CD 1857 XX (the active metabolite of the pro-drug BI 54903 XX) at steady state following inhalation of the fixed dose combination (FDC) of 6.2 μg BI 1744 CL plus 727.3 μg BI 54903 XX (as ethanolic solution for inhalation, EIS) with the systemic exposure following inhalation of the mono compounds of 10 μg BI 1744 CL (as aqueous solution for inhalation, AIS) and 727.3 μg BI 54903 XX (EIS), respectively, when administered once-daily via Respimat® Inhaler (Respimat® A for AIS and Respimat® B for EIS) for 14 days in healthy volunteers. Secondary objectives were to compare exposure to BI 1744 BS and CD 1857 XX after a single dose of the BI 1744 CL/BI 54903 XX (6.2 μg/727.3 μg) FDC and the mono compounds, respectively; to compare exposure to BI 54903 XX after a single dose and at steady state after multiple doses of the BI 1744 CL/BI 54903 XX (6.2 μg/727.3 μg) FDC and the mono compounds, respectively; to compare the safety and tolerability of BI 1744 CL and BI 54903 XX when administered as BI 1744 CL/BI 54903 XX (6.2 μg/727.3 μg) FDC and as the mono compounds, respectively.

Condition or disease Intervention/treatment Phase
Healthy Drug: BI 1744 CL/BI 54903 XX FDC Drug: BI 54903 XX Drug: BI 1744 CL Phase 1

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Study Type : Interventional  (Clinical Trial)
Enrollment : 36 participants
Allocation: Randomized
Intervention Model: Crossover Assignment
Masking: None (Open Label)
Primary Purpose: Treatment
Official Title: An Open Label, Randomised, Three-way Crossover Phase I Study to Assess Safety, Tolerability and Pharmacokinetics of the Fixed Dose Combination of BI 1744 CL Plus BI 54903 XX Via Respimat® B Versus the Mono Products of BI 1744 CL Via Respimat® A and BI 54903 XX Via Respimat® B in Healthy Male and Female Volunteers
Study Start Date : April 2009
Actual Primary Completion Date : July 2009

Resource links provided by the National Library of Medicine


Arm Intervention/treatment
Experimental: BI 1744 CL/BI 54903 XX FDC Drug: BI 1744 CL/BI 54903 XX FDC
Active Comparator: BI 54903 XX Drug: BI 54903 XX
Active Comparator: BI 1744 CL Drug: BI 1744 CL



Primary Outcome Measures :
  1. AUC0-t,ss (area under the concentration time curve of the analyte in plasma from 0 to time t at steady state) [ Time Frame: up to 24 hours after drug administration ]
    for BI 1744 BS and CD 1857 XX

  2. Cmax,ss (maximum measured concentration of the analyte in plasma at steady state) [ Time Frame: up to 24 hours after drug administration ]
    for BI 1744 BS and CD 1857 XX


Secondary Outcome Measures :
  1. AUC0-t (area under the concentration time curve of the analyte in plasma from 0 to time t) [ Time Frame: up to 24 hours after drug administration ]
  2. Cmax (maximum measured concentration of the analyte in plasma) [ Time Frame: up to 24 hours after drug administration ]
    for BI 54903 XX

  3. Cpre (pre-dose concentration of the analyte in plasma (at steady state) [ Time Frame: up to 24 hours after drug administration ]
  4. AUCt1-t2 (area under the concentration time curve of the analyte in plasma over the time interval t1 to t2) [ Time Frame: up to 24 hours after drug administration ]
  5. 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 ]
  6. AUCτ (area under the plasma concentration-time curve over a uniform dosing interval τ) [ Time Frame: up to 24 hours after drug administration ]
  7. 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 ]
  8. %AUCtz-∞ (the percentage of the AUC0-∞ that is obtained by extrapolation) [ Time Frame: up to 24 hours after drug administration ]
  9. tmax (time from dosing to the maximum concentration of the analyte in plasma) [ Time Frame: up to 24 hours after drug administration ]
  10. λz (terminal rate constant of the analyte in plasma) [ Time Frame: up to 24 hours after drug administration ]
  11. t½ (terminal half-life of the analyte in plasma) [ Time Frame: up to 24 hours after drug administration ]
  12. MRTih (mean residence time of the analyte in the body after inhaled administration) [ Time Frame: up to 24 hours after drug administration ]
  13. Aet1-t2 (amount of the analyte that is eliminated in urine from the time point t1 to time point t2) [ Time Frame: up to 24 hours after drug administration ]
  14. fet1-t2 (fraction of the analyte eliminated in urine from time point t1 to time point t2) [ Time Frame: up to 24 hours after drug administration ]
  15. 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 ]
  16. CL/F (apparent clearance of the analyte in the plasma after extravascular administration) [ Time Frame: up to 24 hours after drug administration ]
    For BI 1744 BS and BI 54903 XX only

  17. Vz/F (apparent volume of distribution of the analyte during the terminal phase following an extravascular dose) [ Time Frame: up to 24 hours after drug administration ]
    For BI 1744 BS and BI 54903 XX only

  18. Number of patients with adverse events [ Time Frame: up to 16 weeks ]
  19. Assessment of tolerability by investigator on 4-point scale [ Time Frame: 28 days after each treatment period ]


Information from the National Library of Medicine

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Ages Eligible for Study:   21 Years to 50 Years   (Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   Yes
Criteria

Inclusion Criteria:

  • Healthy males and females according to the following criteria: Based upon a complete medical history, including the physical examination, vital signs (Blood pressure (BP), Pulse Rate (PR)), 12-lead Electrocardiogram (ECG), clinical laboratory tests
  • Age >= 21 and Age <= 50 years
  • Body mass index (BMI) >= 18.5 and <= 29.9 kg/m2
  • 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:

  • Any finding of the medical examination (including Blood pressure (BP), Pulse Rate (PR) and Electrocardiogram (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 h) within at least 1 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 2 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 40 g/day)
  • Drug abuse
  • Blood donation (more than 100 mL within 4 weeks prior to administration or during the trial)
  • Excessive physical activities (within 1 week prior to administration or during the trial)
  • Any laboratory value outside the reference range of clinical relevance
  • Inability to comply with dietary regimen of trial site

For female subjects:

  • Pregnancy or planning to become pregnant within 2 months of study completion
  • Positive pregnancy test
  • No adequate contraception e.g., sterilization, intrauterine device (IUD), oral contraception for at least 3 months prior to participation in the study
  • Inability to maintain this adequate contraception during the whole trial period
  • Lactation period
  • Asthma or history of pulmonary hyperreactivity
  • Hyperthyrosis
  • Allergic rhinitis in need of treatment
  • Clinically relevant cardiac arrhythmia
  • Bacterial and viral infections of the lung including tuberculosis

Additional Information:
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Responsible Party: Boehringer Ingelheim
ClinicalTrials.gov Identifier: NCT02222428     History of Changes
Other Study ID Numbers: 1256.3
First Posted: August 21, 2014    Key Record Dates
Last Update Posted: August 21, 2014
Last Verified: August 2014
Additional relevant MeSH terms:
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Olodaterol
Bronchodilator Agents
Autonomic Agents
Peripheral Nervous System Agents
Physiological Effects of Drugs
Anti-Asthmatic Agents
Respiratory System Agents