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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 octobre 2014 mis à jour par: 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

Aperçu de l'étude

Type d'étude

Interventionnel

Inscription (Réel)

36

Phase

  • La phase 1

Critères de participation

Les chercheurs recherchent des personnes qui correspondent à une certaine description, appelée critères d'éligibilité. Certains exemples de ces critères sont l'état de santé général d'une personne ou des traitements antérieurs.

Critère d'éligibilité

Âges éligibles pour étudier

21 ans à 45 ans (Adulte)

Accepte les volontaires sains

Oui

Sexes éligibles pour l'étude

Homme

La description

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

Plan d'étude

Cette section fournit des détails sur le plan d'étude, y compris la façon dont l'étude est conçue et ce que l'étude mesure.

Comment l'étude est-elle conçue ?

Détails de conception

  • Objectif principal: Traitement
  • Répartition: Randomisé
  • Modèle interventionnel: Affectation parallèle
  • Masquage: Double

Armes et Interventions

Groupe de participants / Bras
Intervention / Traitement
Comparateur placebo: Placebo
Expérimental: BI 1744 CL in combination with Tiotropium

Que mesure l'étude ?

Principaux critères de jugement

Mesure des résultats
Description de la mesure
Délai
Number of subjects with clinically relevant findings in physical examination
Délai: Up to day 32
Up to day 32
Number of subjects with clinically relevant findings in vital signs
Délai: Up to day 32
blood pressure, pulse rate
Up to day 32
Number of subjects with clinically relevant findings in 12-lead ECG
Délai: Up to day 32
Up to day 32
Number of subjects with clinically relevant findings in laboratory tests
Délai: Up to day 32
Up to day 32
Number of subjects witch clinically relevant changes in additional safety laboratory test parameters
Délai: 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
Délai: 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
Délai: Up to day 32
Up to day 32
Global assessment of tolerability by investigator on a 4-point scale
Délai: Up to day 32
Up to day 32

Mesures de résultats secondaires

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

Collaborateurs et enquêteurs

C'est ici que vous trouverez les personnes et les organisations impliquées dans cette étude.

Publications et liens utiles

La personne responsable de la saisie des informations sur l'étude fournit volontairement ces publications. Il peut s'agir de tout ce qui concerne l'étude.

Liens utiles

Dates d'enregistrement des études

Ces dates suivent la progression des dossiers d'étude et des soumissions de résultats sommaires à ClinicalTrials.gov. Les dossiers d'étude et les résultats rapportés sont examinés par la Bibliothèque nationale de médecine (NLM) pour s'assurer qu'ils répondent à des normes de contrôle de qualité spécifiques avant d'être publiés sur le site Web public.

Dates principales de l'étude

Début de l'étude

1 avril 2007

Achèvement primaire (Réel)

1 septembre 2007

Dates d'inscription aux études

Première soumission

7 octobre 2014

Première soumission répondant aux critères de contrôle qualité

7 octobre 2014

Première publication (Estimation)

9 octobre 2014

Mises à jour des dossiers d'étude

Dernière mise à jour publiée (Estimation)

9 octobre 2014

Dernière mise à jour soumise répondant aux critères de contrôle qualité

7 octobre 2014

Dernière vérification

1 octobre 2014

Plus d'information

Ces informations ont été extraites directement du site Web clinicaltrials.gov sans aucune modification. Si vous avez des demandes de modification, de suppression ou de mise à jour des détails de votre étude, veuillez contacter register@clinicaltrials.gov. Dès qu'un changement est mis en œuvre sur clinicaltrials.gov, il sera également mis à jour automatiquement sur notre site Web .

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