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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 ottobre 2014 aggiornato da: 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

Panoramica dello studio

Tipo di studio

Interventistico

Iscrizione (Effettivo)

36

Fase

  • Fase 1

Criteri di partecipazione

I ricercatori cercano persone che corrispondano a una certa descrizione, chiamata criteri di ammissibilità. Alcuni esempi di questi criteri sono le condizioni generali di salute di una persona o trattamenti precedenti.

Criteri di ammissibilità

Età idonea allo studio

Da 21 anni a 45 anni (Adulto)

Accetta volontari sani

Sessi ammissibili allo studio

Maschio

Descrizione

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

Piano di studio

Questa sezione fornisce i dettagli del piano di studio, compreso il modo in cui lo studio è progettato e ciò che lo studio sta misurando.

Come è strutturato lo studio?

Dettagli di progettazione

  • Scopo principale: Trattamento
  • Assegnazione: Randomizzato
  • Modello interventistico: Assegnazione parallela
  • Mascheramento: Doppio

Armi e interventi

Gruppo di partecipanti / Arm
Intervento / Trattamento
Comparatore placebo: Placebo
Sperimentale: BI 1744 CL in combination with Tiotropium

Cosa sta misurando lo studio?

Misure di risultato primarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Number of subjects with clinically relevant findings in physical examination
Lasso di tempo: Up to day 32
Up to day 32
Number of subjects with clinically relevant findings in vital signs
Lasso di tempo: Up to day 32
blood pressure, pulse rate
Up to day 32
Number of subjects with clinically relevant findings in 12-lead ECG
Lasso di tempo: Up to day 32
Up to day 32
Number of subjects with clinically relevant findings in laboratory tests
Lasso di tempo: Up to day 32
Up to day 32
Number of subjects witch clinically relevant changes in additional safety laboratory test parameters
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: Up to day 32
Up to day 32
Global assessment of tolerability by investigator on a 4-point scale
Lasso di tempo: Up to day 32
Up to day 32

Misure di risultato secondarie

Misura del risultato
Lasso di tempo
Maximum concentration in plasma (Cmax)
Lasso di tempo: 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)
Lasso di tempo: 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)
Lasso di tempo: 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-∞)
Lasso di tempo: 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-∞)
Lasso di tempo: up to 504 hours after start of treatment
up to 504 hours after start of treatment
Terminal rate constant in plasma (λz)
Lasso di tempo: up to 504 hours after start of treatment
up to 504 hours after start of treatment
Terminal half-life in plasma (t½)
Lasso di tempo: 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)
Lasso di tempo: up to 504 hours after start of treatment
up to 504 hours after start of treatment
Apparent clearance after extravascular administration (CL/F)
Lasso di tempo: 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)
Lasso di tempo: 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)
Lasso di tempo: 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)
Lasso di tempo: 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)
Lasso di tempo: 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)
Lasso di tempo: 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)
Lasso di tempo: Pre-dose every 24 hours
Pre-dose every 24 hours
Time of last measurable concentration in plasma (tz)
Lasso di tempo: up to 504 hours after start of treatment
up to 504 hours after start of treatment
Linearity index (LI)
Lasso di tempo: up to 504 hours after start of treatment
up to 504 hours after start of treatment
Accumulation ratio based on Cmax (RA,Cmax)
Lasso di tempo: up to 504 hours after start of treatment
up to 504 hours after start of treatment
Accumulation ratio based on AUCτ (RA,AUC)
Lasso di tempo: up to 504 hours after start of treatment
up to 504 hours after start of treatment

Collaboratori e investigatori

Qui è dove troverai le persone e le organizzazioni coinvolte in questo studio.

Pubblicazioni e link utili

La persona responsabile dell'inserimento delle informazioni sullo studio fornisce volontariamente queste pubblicazioni. Questi possono riguardare qualsiasi cosa relativa allo studio.

Collegamenti utili

Studiare le date dei record

Queste date tengono traccia dell'avanzamento della registrazione dello studio e dell'invio dei risultati di sintesi a ClinicalTrials.gov. I record degli studi e i risultati riportati vengono esaminati dalla National Library of Medicine (NLM) per assicurarsi che soddisfino specifici standard di controllo della qualità prima di essere pubblicati sul sito Web pubblico.

Studia le date principali

Inizio studio

1 aprile 2007

Completamento primario (Effettivo)

1 settembre 2007

Date di iscrizione allo studio

Primo inviato

7 ottobre 2014

Primo inviato che soddisfa i criteri di controllo qualità

7 ottobre 2014

Primo Inserito (Stima)

9 ottobre 2014

Aggiornamenti dei record di studio

Ultimo aggiornamento pubblicato (Stima)

9 ottobre 2014

Ultimo aggiornamento inviato che soddisfa i criteri QC

7 ottobre 2014

Ultimo verificato

1 ottobre 2014

Maggiori informazioni

Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .

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