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- Essai clinique NCT02171806
Safety, Tolerability, Pharmacokinetics and Pharmacodynamics Study of BI 1744 CL in Healthy Male and Female Volunteers
20 juin 2014 mis à jour par: 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
Aperçu de l'étude
Statut
Complété
Les conditions
Intervention / Traitement
Type d'étude
Interventionnel
Inscription (Réel)
47
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 50 ans (Adulte)
Accepte les volontaires sains
Non
Sexes éligibles pour l'étude
Tout
La description
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
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 multiple rising doses
|
|
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Expérimental: BI 1744 CL medium dose, females
|
Que mesure l'étude ?
Principaux critères de jugement
Mesure des résultats |
Délai |
|---|---|
|
Number of patients with clinically significant changes in physical examination
Délai: Baseline, day 32 (end-of-study examination)
|
Baseline, day 32 (end-of-study examination)
|
|
Number of patients with clinically significant changes in vital signs
Délai: Baseline, up to day 32
|
Baseline, up to day 32
|
|
Number of patients with clinically significant changes in 12-lead ECG (Electrocardiogram)
Délai: Baseline, up to day 32
|
Baseline, up to day 32
|
|
Number of patients with abnormal changes in laboratory tests
Délai: Baseline, up to day 32
|
Baseline, up to day 32
|
|
Changes in airway resistance (Raw) measured by body plethysmography
Délai: Baseline, up to day 32
|
Baseline, up to day 32
|
|
Changes in tremormetry parameters
Délai: Baseline, up to day 32
|
Baseline, up to day 32
|
|
Number of patients with adverse events
Délai: Up to day 32
|
Up to day 32
|
|
Assessment of tolerability by the investigator on a 4-point scale
Délai: Day 32 (end-of-study examination)
|
Day 32 (end-of-study examination)
|
Mesures de résultats secondaires
Mesure des résultats |
Délai |
|---|---|
|
Cmax (maximum concentration of the analyte in plasma)
Délai: Up to 408 hours after drug administration
|
Up to 408 hours after drug administration
|
|
tmax (time from dosing to maximum concentration)
Délai: 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)
Délai: 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)
Délai: 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)
Délai: 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)
Délai: Up to 408 hours after drug administration
|
Up to 408 hours after drug administration
|
|
λz (terminal rate constant of the analyte in plasma)
Délai: Up to 408 hours after drug administration
|
Up to 408 hours after drug administration
|
|
t½ (terminal half-life of the analyte in plasma)
Délai: 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)
Délai: 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)
Délai: 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)
Délai: 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)
Délai: 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)
Délai: Up to 408 hours after drug administration
|
Up to 408 hours after drug administration
|
|
RA,AUC,14 based on AUC0-τ
Délai: 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)
Délai: 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)
Délai: Up to 408 hours after drug administration
|
Up to 408 hours after drug administration
|
|
Linearity Index (LI)
Délai: Up to 408 hours after drug administration
|
Up to 408 hours after drug administration
|
Collaborateurs et enquêteurs
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Publications et liens utiles
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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 janvier 2006
Achèvement primaire (Réel)
1 septembre 2006
Dates d'inscription aux études
Première soumission
20 juin 2014
Première soumission répondant aux critères de contrôle qualité
20 juin 2014
Première publication (Estimation)
24 juin 2014
Mises à jour des dossiers d'étude
Dernière mise à jour publiée (Estimation)
24 juin 2014
Dernière mise à jour soumise répondant aux critères de contrôle qualité
20 juin 2014
Dernière vérification
1 juin 2014
Plus d'information
Termes liés à cette étude
Termes MeSH pertinents supplémentaires
Autres numéros d'identification d'étude
- 1222.2
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