- ICH GCP
- US-Register für klinische Studien
- Klinische Studie NCT02259959
Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of Multiple Rising Inhalative Doses of BI 1744 CL in Fixed Dose Combination With Tiotropium Bromide in Healthy Male Volunteers
7. Oktober 2014 aktualisiert von: Boehringer Ingelheim
Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of Multiple Rising Inhalative Doses (2 μg/5 μg, 10 μg/5 μg, and 40 μg/10 μg) of BI 1744 CL in Fixed Dose Combination With Tiotropium Bromide for 14 Days in Healthy Male Volunteers (Double-blind, Randomised, Placebo Controlled [at Each Dose Level] Study)
To investigate safety, tolerability, pharmacokinetics and pharmacodynamics of BI 1744 CL and Tiotropium Bromide when given as fixed dose combination
Studienübersicht
Status
Abgeschlossen
Bedingungen
Studientyp
Interventionell
Einschreibung (Tatsächlich)
36
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 45 Jahre (Erwachsene)
Akzeptiert gesunde Freiwillige
Ja
Studienberechtigte Geschlechter
Männlich
Beschreibung
Inclusion Criteria:
- Healthy male based upon a complete medical history, including 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
- Age ≥21 and ≤45 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 (GCP) 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 randomization
- 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 40 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)
The following exclusion criteria are specific for this study due to the known class side effect profile of Tiotropium:
- Hypersensitivity to tiotropium and/or related drugs of these classes
- History of narrow-angle glaucoma
- History of prostatic hyperplasia
- History of bladder-neck obstruction
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 in combination with Tiotropium
|
Was misst die Studie?
Primäre Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
|---|---|---|
|
Number of subjects with clinically relevant findings in physical examination
Zeitfenster: Up to day 32
|
Up to day 32
|
|
|
Number of subjects with clinically relevant findings in vital signs
Zeitfenster: Up to day 32
|
blood pressure, pulse rate
|
Up to day 32
|
|
Number of subjects with clinically relevant findings in 12-lead ECG
Zeitfenster: Up to day 32
|
Up to day 32
|
|
|
Number of subjects with clinically relevant findings in laboratory tests
Zeitfenster: Up to day 32
|
Up to day 32
|
|
|
Number of subjects witch clinically relevant changes in additional safety laboratory test parameters
Zeitfenster: up to 318 hours after start of treatment
|
Systemic metabolic parameters: cyclic adenosine mono phosphate (cAMP) and potassium
|
up to 318 hours after start of treatment
|
|
Number of subjects with clinically relevant changes in airway resistance (Raw) measured by body plethysmography
Zeitfenster: Pre-dose, up to 408 hours after start of treatment
|
Pre-dose, up to 408 hours after start of treatment
|
|
|
Number of subjects with adverse events
Zeitfenster: Up to day 32
|
Up to day 32
|
|
|
Global assessment of tolerability by investigator on a 4-point scale
Zeitfenster: Up to day 32
|
Up to day 32
|
Sekundäre Ergebnismessungen
Ergebnis Maßnahme |
Zeitfenster |
|---|---|
|
Maximum concentration in plasma (Cmax)
Zeitfenster: up to 504 hours after start of treatment
|
up to 504 hours after start of treatment
|
|
Time from dosing to maximum concentration in plasma (tmax)
Zeitfenster: up to 504 hours after start of treatment
|
up to 504 hours after start of treatment
|
|
Area under the concentration-time curve in plasma (AUC)
Zeitfenster: up to 504 hours after start of treatment
|
up to 504 hours after start of treatment
|
|
Area under the concentration-time curve in plasma over the time interval from 0 extrapolated to infinity (AUC0-∞)
Zeitfenster: up to 504 hours after start of treatment
|
up to 504 hours after start of treatment
|
|
Percentage of AUC 0-∞ that is obtained by extrapolation (%AUCtz-∞)
Zeitfenster: up to 504 hours after start of treatment
|
up to 504 hours after start of treatment
|
|
Terminal rate constant in plasma (λz)
Zeitfenster: up to 504 hours after start of treatment
|
up to 504 hours after start of treatment
|
|
Terminal half-life in plasma (t½)
Zeitfenster: up to 504 hours after start of treatment
|
up to 504 hours after start of treatment
|
|
Mean residence time in the body after inhalation (MRTih)
Zeitfenster: up to 504 hours after start of treatment
|
up to 504 hours after start of treatment
|
|
Apparent clearance after extravascular administration (CL/F)
Zeitfenster: up to 504 hours after start of treatment
|
up to 504 hours after start of treatment
|
|
Apparent volume of distribution during the terminal phase λz following an extravascular dose (Vz/F)
Zeitfenster: up to 504 hours after start of treatment
|
up to 504 hours after start of treatment
|
|
Amount eliminated in urine from the time point t1 to t2 (Aet1-t2)
Zeitfenster: up to 336 hours after start of treatment
|
up to 336 hours after start of treatment
|
|
Fraction excreted in urine from time point t1 to t2 (fet1-t2)
Zeitfenster: up to 336 hours after start of treatment
|
up to 336 hours after start of treatment
|
|
Renal clearance from the time point t1 until the time point t2 (CLR,t1-t2)
Zeitfenster: up to 504 hours after start of treatment
|
up to 504 hours after start of treatment
|
|
Minimum measured concentration in plasma at steady state over a uniform dosing interval τ (Cmin,ss)
Zeitfenster: up to 504 hours after start of treatment
|
up to 504 hours after start of treatment
|
|
Predose concentration of the analytes in plasma at steady state immediately before administration of the next dose (Cpre,ss)
Zeitfenster: Pre-dose every 24 hours
|
Pre-dose every 24 hours
|
|
Time of last measurable concentration in plasma (tz)
Zeitfenster: up to 504 hours after start of treatment
|
up to 504 hours after start of treatment
|
|
Linearity index (LI)
Zeitfenster: up to 504 hours after start of treatment
|
up to 504 hours after start of treatment
|
|
Accumulation ratio based on Cmax (RA,Cmax)
Zeitfenster: up to 504 hours after start of treatment
|
up to 504 hours after start of treatment
|
|
Accumulation ratio based on AUCτ (RA,AUC)
Zeitfenster: up to 504 hours after start of treatment
|
up to 504 hours after start of treatment
|
Mitarbeiter und Ermittler
Hier finden Sie Personen und Organisationen, die an dieser Studie beteiligt sind.
Sponsor
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. April 2007
Primärer Abschluss (Tatsächlich)
1. September 2007
Studienanmeldedaten
Zuerst eingereicht
7. Oktober 2014
Zuerst eingereicht, das die QC-Kriterien erfüllt hat
7. Oktober 2014
Zuerst gepostet (Schätzen)
9. Oktober 2014
Studienaufzeichnungsaktualisierungen
Letztes Update gepostet (Schätzen)
9. Oktober 2014
Letztes eingereichtes Update, das die QC-Kriterien erfüllt
7. Oktober 2014
Zuletzt verifiziert
1. Oktober 2014
Mehr Informationen
Begriffe im Zusammenhang mit dieser Studie
Zusätzliche relevante MeSH-Bedingungen
- Physiologische Wirkungen von Arzneimitteln
- Neurotransmitter-Agenten
- Molekulare Mechanismen der pharmakologischen Wirkung
- Parasympatholytika
- Autonome Agenten
- Agenten des peripheren Nervensystems
- Cholinerge Antagonisten
- Cholinerge Wirkstoffe
- Bronchodilatatoren
- Anti-Asthmatiker
- Atemwegsmittel
- Pharmazeutische Lösungen
- Tiotropiumbromid
- Olodaterol
Andere Studien-ID-Nummern
- 1237.2
Diese Informationen wurden ohne Änderungen direkt von der Website clinicaltrials.gov abgerufen. Wenn Sie Ihre Studiendaten ändern, entfernen oder aktualisieren möchten, wenden Sie sich bitte an register@clinicaltrials.gov. Sobald eine Änderung auf clinicaltrials.gov implementiert wird, wird diese automatisch auch auf unserer Website aktualisiert .
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