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Safety, Tolerability, Pharmacokinetics and Pharmacodynamics Study of BI 1744 CL in Healthy Male and Female Volunteers

20. Juni 2014 aktualisiert von: Boehringer Ingelheim

Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of Multiple Rising Inhalative Doses (2.5 μg, 10 μg, and 30 μg) of BI 1744 CL for 14 Days in Healthy Male and Female Volunteers (Doubleblind, Randomised, Placebo Controlled [at Each Dose Level] Study)

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

Studienübersicht

Status

Abgeschlossen

Bedingungen

Studientyp

Interventionell

Einschreibung (Tatsächlich)

47

Phase

  • Phase 1

Teilnahmekriterien

Forscher suchen nach Personen, die einer bestimmten Beschreibung entsprechen, die als Auswahlkriterien bezeichnet werden. Einige Beispiele für diese Kriterien sind der allgemeine Gesundheitszustand einer Person oder frühere Behandlungen.

Zulassungskriterien

Studienberechtigtes Alter

21 Jahre bis 50 Jahre (Erwachsene)

Akzeptiert gesunde Freiwillige

Nein

Studienberechtigte Geschlechter

Alle

Beschreibung

Inclusion Criteria:

  • Healthy male or female based upon a complete medical history, including the physical examination, regarding vital signs (blood pressure (BP), pulse rate (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.
  • Age ≥21 and ≤50 years
  • BMI ≥18.5 and <30 kg/m2 (Body Mass Index)
  • Signed and dated written informed consent prior to admission to the study in accordance with Good Clinical Practice and the local legislation

Exclusion Criteria:

  • Any finding of the medical examination (including BP, PR, and ECG measurements) deviating from normal and of clinical relevance
  • Evidence of a clinically relevant concomitant disease
  • 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 relevant orthostatic hypotension, fainting spells or blackouts
  • Chronic or relevant acute infections
  • History of relevant allergy/hypersensitivity (including allergy to the drug or its excipients) as judged clinically relevant by the investigator
  • Intake of drugs with a long half-life (>24 hours) within at least 1 month or less than 10 half-lives of the respective drug prior to randomisation
  • Use of 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
  • Participation in another trial with an investigational drug within 2 months prior to randomisation
  • Smoker (>10 cigarettes or >3 cigars or >3 pipes/day)
  • Inability to refrain from smoking on trial days as judged by the investigator
  • Alcohol abuse (more than 60 g alcohol a day)
  • Drug abuse
  • Blood donation (more than 100 mL blood within 4 weeks prior to randomisation or during the trial)
  • Excessive physical activities within 1 week prior to randomisation or during the trial
  • Any laboratory value outside the reference range that is of clinical relevance
  • Inability to comply with dietary regimen of the study centre

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

  • Asthma or history of pulmonary hyperreactivity
  • Hyperthyrosis
  • Allergic rhinitis in need of treatment
  • Clinically relevant cardiac arrhythmia
  • 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 2 months after release from the study.
  • Inability to maintain this adequate contraception during the whole study period
  • Lactation period

Studienplan

Dieser Abschnitt enthält Einzelheiten zum Studienplan, einschließlich des Studiendesigns und der Messung der Studieninhalte.

Wie ist die Studie aufgebaut?

Designdetails

  • Hauptzweck: Behandlung
  • Zuteilung: Zufällig
  • Interventionsmodell: Parallele Zuordnung
  • Maskierung: Doppelt

Waffen und Interventionen

Teilnehmergruppe / Arm
Intervention / Behandlung
Placebo-Komparator: Placebo
Experimental: BI 1744 CL multiple rising doses
Experimental: BI 1744 CL medium dose, females

Was misst die Studie?

Primäre Ergebnismessungen

Ergebnis Maßnahme
Zeitfenster
Number of patients with clinically significant changes in physical examination
Zeitfenster: Baseline, day 32 (end-of-study examination)
Baseline, day 32 (end-of-study examination)
Number of patients with clinically significant changes in vital signs
Zeitfenster: Baseline, up to day 32
Baseline, up to day 32
Number of patients with clinically significant changes in 12-lead ECG (Electrocardiogram)
Zeitfenster: Baseline, up to day 32
Baseline, up to day 32
Number of patients with abnormal changes in laboratory tests
Zeitfenster: Baseline, up to day 32
Baseline, up to day 32
Changes in airway resistance (Raw) measured by body plethysmography
Zeitfenster: Baseline, up to day 32
Baseline, up to day 32
Changes in tremormetry parameters
Zeitfenster: Baseline, up to day 32
Baseline, up to day 32
Number of patients with adverse events
Zeitfenster: Up to day 32
Up to day 32
Assessment of tolerability by the investigator on a 4-point scale
Zeitfenster: Day 32 (end-of-study examination)
Day 32 (end-of-study examination)

Sekundäre Ergebnismessungen

Ergebnis Maßnahme
Zeitfenster
Cmax (maximum concentration of the analyte in plasma)
Zeitfenster: Up to 408 hours after drug administration
Up to 408 hours after drug administration
tmax (time from dosing to maximum concentration)
Zeitfenster: Up to 408 hours after drug administration
Up to 408 hours after drug administration
AUC (area under the concentration-time curve of the analyte in plasma at different time points)
Zeitfenster: Up to 408 hours after drug administration
Up to 408 hours after drug administration
Aet1-t2(amount of analyte that is eliminated in urine from the time point t1 to time point t2)
Zeitfenster: Up to 384 hours after drug administration
Up to 384 hours after drug administration
fet1-t2 (fraction of analyte eliminated in urine from time point t1 to time point t2)
Zeitfenster: Up to 384 hours after drug administration
Up to 384 hours after drug administration
%AUCtz-∞ (the percentage of the AUC 0-∞ that is obtained by extrapolation)
Zeitfenster: Up to 408 hours after drug administration
Up to 408 hours after drug administration
λz (terminal rate constant of the analyte in plasma)
Zeitfenster: Up to 408 hours after drug administration
Up to 408 hours after drug administration
t½ (terminal half-life of the analyte in plasma)
Zeitfenster: Up to 408 hours after drug administration
Up to 408 hours after drug administration
MRTih (mean residence time of the analyte in the body after inhalation)
Zeitfenster: Up to 408 hours after drug administration
Up to 408 hours after drug administration
CL/F (apparent clearance of the analyte in the plasma after extravascular administration)
Zeitfenster: Up to 408 hours after drug administration
Up to 408 hours after drug administration
Vz/F (apparent volume of distribution of the analyte during the terminal phase λz following an extravascular dose)
Zeitfenster: Up to 408 hours after drug administration
Up to 408 hours after drug administration
CLR,t1-t2 (renal clearance of the analyte in plasma from the time point t1 until the time point t2)
Zeitfenster: Up to 408 hours after drug administration
Up to 408 hours after drug administration
RA,Cmax,14 based on Cmax (Accumulation ratio of the analyte in plasma after multiple dose administration over a uniform dosing interval τ)
Zeitfenster: Up to 408 hours after drug administration
Up to 408 hours after drug administration
RA,AUC,14 based on AUC0-τ
Zeitfenster: Up to 408 hours after drug administration
Up to 408 hours after drug administration
Cmin,ss (minimum measured concentration of the analyte in plasma at steady state over a uniform dosing interval τ)
Zeitfenster: Up to 408 hours after drug administration
Up to 408 hours after drug administration
Cpre,ss (predose concentration of the analyte in plasma at steady state immediately before administration of the next dose)
Zeitfenster: Up to 408 hours after drug administration
Up to 408 hours after drug administration
Linearity Index (LI)
Zeitfenster: Up to 408 hours after drug administration
Up to 408 hours after drug administration

Mitarbeiter und Ermittler

Hier finden Sie Personen und Organisationen, die an dieser Studie beteiligt sind.

Publikationen und hilfreiche Links

Die Bereitstellung dieser Publikationen erfolgt freiwillig durch die für die Eingabe von Informationen über die Studie verantwortliche Person. Diese können sich auf alles beziehen, was mit dem Studium zu tun hat.

Nützliche Links

Studienaufzeichnungsdaten

Diese Daten verfolgen den Fortschritt der Übermittlung von Studienaufzeichnungen und zusammenfassenden Ergebnissen an ClinicalTrials.gov. Studienaufzeichnungen und gemeldete Ergebnisse werden von der National Library of Medicine (NLM) überprüft, um sicherzustellen, dass sie bestimmten Qualitätskontrollstandards entsprechen, bevor sie auf der öffentlichen Website veröffentlicht werden.

Haupttermine studieren

Studienbeginn

1. Januar 2006

Primärer Abschluss (Tatsächlich)

1. September 2006

Studienanmeldedaten

Zuerst eingereicht

20. Juni 2014

Zuerst eingereicht, das die QC-Kriterien erfüllt hat

20. Juni 2014

Zuerst gepostet (Schätzen)

24. Juni 2014

Studienaufzeichnungsaktualisierungen

Letztes Update gepostet (Schätzen)

24. Juni 2014

Letztes eingereichtes Update, das die QC-Kriterien erfüllt

20. Juni 2014

Zuletzt verifiziert

1. Juni 2014

Mehr Informationen

Begriffe im Zusammenhang mit dieser Studie

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