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A Study to Assess Safety, Tolerability and Pharmacokinetics of Single Rising Inhaled Doses of BI 1744 CL in Healthy Male and Female Volunteers

Phase 1
Completed
Conditions
Healthy
Interventions
Drug: BI 1744 CL
Drug: Placebo
Registration Number
NCT02171780
Lead Sponsor
Boehringer Ingelheim
Brief Summary

To investigate safety, tolerability, and pharmacokinetics of BI 1744 CL

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
122
Inclusion Criteria
  • The subject is healthy based upon a complete medical history, including the physical examination, regarding vital signs (BP, PR), 12-lead ECG measurement, and clinical laboratory tests. There is no finding deviating from normal and of clinical relevance. There is no evidence of a clinically relevant concomitant disease
  • The subject is at least 21 years old and not older than 50 years
  • The subject's body mass index (BMI) is at least 18.5 kg/m2 and less than 30 kg/m2
  • The subject has signed and dated a written informed consent prior to admission to the study in accordance with GCP (Good Clinical Practice) and the local legislation
Exclusion Criteria
  • The subject has any finding of the medical examination (including BP, PR, and ECG measurements) deviating from normal and of clinical relevance
  • The subject had a surgery of gastrointestinal tract (except appendectomy)
  • The subject has a diagnosis of gastrointestinal, hepatic, renal, respiratory, cardiovascular, metabolic, immunological or hormonal disorders
  • The subject has a diagnosis of diseases of the central nervous system (such as epilepsy) or psychiatric disorders or neurological disorders
  • The subject has a history of relevant orthostatic hypotension, fainting spells or blackouts
  • The subject has a diagnosis of chronic or relevant acute infections
  • The subject has a history of relevant allergy/hypersensitivity (including allergy to the drug or its excipients) as judged clinically relevant by the investigator
  • The subject has taken 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 randomisation
  • The subject has used 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 randomisation
  • The subject has participated in another trial with an investigational drug within two months prior to randomisation
  • The subject is a heavily smoker (>10 cigarettes or >3 cigars or >3 pipes/day)
  • The subject is not able to refrain from smoking on trial days as judged by the investigator
  • The subject uses more than 60 g alcohol a day)
  • The subject uses drugs
  • The subject has donated more than 100 mL blood within four weeks prior to randomisation
  • The subject has performed excessive physical activities within one week prior to randomisation
  • The subject has a laboratory value outside the reference range that is of clinical relevance
  • The subject is not able to comply with dietary regimen of the study centre.

The following exclusion criteria were specific for this study due to the known class side effect profile of ß2-mimetics:

  • The subject has a diagnosis of asthma or history of pulmonary hyperreactivity
  • The subject has a diagnosis of hyperthyrosis
  • The subject has a diagnosis of allergic rhinitis in need of treatment
  • The subject has a diagnosis of clinically relevant cardiac arrhythmia
  • The subject has a diagnosis of paroxysmal tachycardia (>100 beats per minute).

For female subjects:

  • Pregnancy
  • Positive pregnancy test
  • No adequate contraception e.g. oral contraception, sterilisation, IUD (intrauterine device). Females who are not surgically sterile will be asked to additionally use barrier contraception methods (e.g. condoms) prior to administration of study medication, during the study and at least one month after release from the study
  • Inability to maintain this adequate contraception during the whole study period
  • Lactation period

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
BI 1744 CL single rising dosesBI 1744 CL-
PlaceboPlacebo-
Primary Outcome Measures
NameTimeMethod
Number of patients with clinically significant changes in vital signsBaseline, up to 12 days after drug administration
Number of patients with abnormal findings in physical examination12 days after drug administration
Change in orthostasis test parametersBaseline, up to 24 hours after drug administration
Number of patients with adverse eventsUp to 12 days
Number of patients with abnormal changes in laboratory parametersBaseline, up to 12 days after drug administration
Number of patients with abnormal changes in 12-lead ECG (electrocardiogram) parametersBaseline, up to 12 days after drug administration
Number of patients with abnormal findings of pulmonary auscultationBaseline, up to 24 hours after drug administration
Change in airway resistance (Raw), as measured by body plethysmographyBaseline, up to 24 hours after drug administration
Assessment of tolerability by investigator on a 4-point scale12 days after drug administration
Change in oral body temperatureBaseline, up to 24 hours after drug administration
Change in tremormetry parametersBaseline, up to 24 hours after drug administration
Number of patients with abnormal findings of oropharyngeal inspectionBaseline, up to 24 hours after drug administration
Secondary Outcome Measures
NameTimeMethod
Time from dosing to maximum concentration (tmax)Up to 96 hours after drug administration
Fraction of BI 1744 CL eliminated in urine from time point t1 to time point t2 (fet1-t2)Up to 96 hours after drug administration
Terminal rate constant of BI 1744 CL in plasma (λz)Up to 96 hours after drug administration
Area under the concentration-time curve of BI 1744 CL in plasma over the time interval from 0 to 24 hours (AUC0-24)Up to 96 hours after drug administration
Amount of BI 1744 CLeliminated in urine from the time point t1 to time point t2 (Aet1-t2)Up to 96 hours after drug administration
Renal clearance of BI 1744 CL from 0 to 24 hours (CLR,0-24)Up to 24 hours after drug administration
Terminal half-life of BI 1744 CL in plasma (t½)Up to 96 hours after drug administration
Maximum concentration of BI 1744 CL in plasma (Cmax)Up to 96 hours after drug administration
Area under the concentration-time curve of BI 1744 CL in plasma over the time interval from 0 extrapolated to infinity (AUC0-∞)Up to 96 hours after drug administration
Area under the concentration-time curve of BI 1744 CL in plasma over the time interval from 0 to the time of the last quantifiable data point (AUC0-tz)Up to 96 hours after drug administration
Apparent volume of distribution of BI 1744 CL during the terminal phase λz following an extravascular dose (Vz/F)Up to 96 hours after drug administration
AUC0-tz over AUC0-∞ (%AUC0-tz)Up to 96 hours after drug administration
Mean residence time of BI 1744 CL in the body after inhalation (MRTih)Up to 96 hours after drug administration
Apparent clearance of BI 1744 CL in the plasma after extravascular administration (CL/F)Up to 96 hours after drug administration
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