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Multiple Rising Oral Doses of BI 691751 in Healthy Male Subjects

1 février 2016 mis à jour par: Boehringer Ingelheim

Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of Multiple Rising Oral Doses of BI 691751 in Healthy Male Subjects

It is the objective of this MRD trial to investigate pharmacokinetics, pharmcodynamics, safety and tolerability of rising doses BI 691751 over a treatment period of 14 days to support the further clinical development of this LTA4H-inhibitor. Special emphasis will be given to detect potential effects of BI 691751 on heart rate.

Aperçu de l'étude

Type d'étude

Interventionnel

Inscription (Réel)

18

Phase

  • La phase 1

Contacts et emplacements

Cette section fournit les coordonnées de ceux qui mènent l'étude et des informations sur le lieu où cette étude est menée.

Lieux d'étude

      • Berlin, Allemagne
        • 1334.2.1 Boehringer Ingelheim Investigational Site

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

18 ans à 50 ans (Adulte)

Accepte les volontaires sains

Oui

Sexes éligibles pour l'étude

Homme

La description

Inclusion criteria:

  • Healthy male subjects according to the investigator´s assessment, based on a complete medical history including a physical examination, vital signs (BP (blood pressure), PR (pulse rate), 12-lead ECG (electro cardiogramm), and clinical laboratory tests
  • Age of 18 to 50 years (incl.)
  • BMI (body mass index) of 18.5 to 29.9 kg/m2 (incl.)
  • Signed and dated written informed consent prior to admission to the study in accordance with GCP(Good Clinical Practice) and local legislation
  • Subject is able to understand and communicate in German

Exclusion criteria:

  • Any finding in the medical examination (including BP (blood pressure), PR (pulse rate) or ECG (electro cardiogramm) is deviating from normal and judged as clinically relevant by the investigator
  • Pulse rate outside 45-80 bpm (beats per minutes) or repeated measurement of systolic blood pressure greater than 140 mmHg, diastolic blood pressure greater than 90 mm Hg
  • Any laboratory value outside the reference range that the investigator considers to be of clinical relevance
  • Any evidence of a concomitant disease judged as clinically relevant by the investigator
  • Gastrointestinal, hepatic, renal, respiratory, cardiovascular, metabolic, immunological or hormonal disorders
  • Surgery of the gastrointestinal tract that could interfere with kinetics of the trial medication
  • Diseases of the central nervous system (such as epilepsy), other neurological disorders or psychiatric disorders
  • History of relevant orthostatic hypotension, fainting spells, or blackouts
  • Chronic or relevant acute infections
  • History of relevant allergy or hypersensitivity (including allergy to the trial medication or its excipients)
  • Intake of drugs with a long half-life (more than 24 h) within 30 days or less than 10 half-lives of the respective drug prior to administration of trial medication
  • Within 10 days prior to administration of trial medication, use of drugs that might reasonably influence the results of the trial or that might prolong the QT/QTc interval
  • Participation in another trial where an investigational drug has been administered within 60 days prior to planned administration of trial medication
  • Smoker (more than 10 cigarettes or 3 cigars or 3 pipes per day)
  • Inability to refrain from smoking during inhouse-confinement
  • Alcohol abuse (consumption of more 30 g per day for males)
  • Drug abuse or positive drug screening
  • Blood donation of more than 100 mL within 30 days prior to administration of trial medication or intended donation during the trial
  • Intention to perform excessive physical activities within one week prior to administration of trial medication or during the trial
  • Inability to comply with dietary regimen of trial site
  • A marked baseline prolongation of QT/QTc interval (such as QTc intervals that are repeatedly greater than 450 ms in males) or any other relevant ECG finding at screening
  • A history of additional risk factors for Torsades de Pointes (such as heart failure, hypokalemia, or family history of Long QT Syndrome)
  • Subject is assessed as unsuitable for inclusion by the investigator, for instance, because considered not able to understand and comply with study requirements, or has a condition that would not allow safe participation in the study
  • Vulnerable subjects, e.g. subjects kept in detention, soldiers, employees of the sponsor or a clinical research organization, involved in this study

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
Placebo
Expérimental: BI 691751 Dose 1
multiple dose given over 14 days
BI 691751 Dose 1
BI 691751 Dose 2
BI 691751 Dose 3
BI 691751 Dose 4
BI 691751 Dose 5
BI 691751 Dose 6
Expérimental: BI 691751 Dose 2
multiple dose given over 14 days
BI 691751 Dose 1
BI 691751 Dose 2
BI 691751 Dose 3
BI 691751 Dose 4
BI 691751 Dose 5
BI 691751 Dose 6
Expérimental: BI 691751 Dose 3
multiple dose given over 14 days
BI 691751 Dose 1
BI 691751 Dose 2
BI 691751 Dose 3
BI 691751 Dose 4
BI 691751 Dose 5
BI 691751 Dose 6
Expérimental: BI 691751 Dose 4
multiple dose given over 14 days
BI 691751 Dose 1
BI 691751 Dose 2
BI 691751 Dose 3
BI 691751 Dose 4
BI 691751 Dose 5
BI 691751 Dose 6
Expérimental: BI 691751 Dose 5
multiple dose given over 14 days
BI 691751 Dose 1
BI 691751 Dose 2
BI 691751 Dose 3
BI 691751 Dose 4
BI 691751 Dose 5
BI 691751 Dose 6
Expérimental: BI 691751 Dose 6
multiple dose given over 14 days
BI 691751 Dose 1
BI 691751 Dose 2
BI 691751 Dose 3
BI 691751 Dose 4
BI 691751 Dose 5
BI 691751 Dose 6

Que mesure l'étude ?

Principaux critères de jugement

Mesure des résultats
Description de la mesure
Délai
Percentage of Subjects With Drug-related Adverse Events
Délai: From the time of administration of the respective treatment until 21 days after last administration of study drug or start of the post-study phase to the respective treatment, up to 35 days
Percentage of subjects with drug-related Adverse events (AEs)
From the time of administration of the respective treatment until 21 days after last administration of study drug or start of the post-study phase to the respective treatment, up to 35 days

Mesures de résultats secondaires

Mesure des résultats
Description de la mesure
Délai
AUCt,1 (Area Under the Concentration-time Curve of the Analyte in Plasma Over a Uniform Dosing Interval t After Administration of the First Dose)
Délai: 0 minutes (min), 10min, 20min, 40min, 1 hour (h), 1h 30min, 2h, 3h, 4h, 6h, 8h, 10h, 12h and 24h after first drug administration

AUCt,1 (area under the concentration-time curve of the analyte in plasma over a uniform dosing interval t after administration of the first dose).

This endpoint could not be calculated as no PK blood samples were analysed due to the early termination of the study.

0 minutes (min), 10min, 20min, 40min, 1 hour (h), 1h 30min, 2h, 3h, 4h, 6h, 8h, 10h, 12h and 24h after first drug administration
Cmax (Maximum Measured Concentration of the Analyte Inplasma)
Délai: 0 minutes (min), 10min, 20min, 40min, 1 hour (h), 1h 30min, 2h, 3h, 4h, 6h, 8h, 10h, 12h and 24h after first drug administration

Cmax (maximum measured concentration of the analyte inplasma).

This endpoint could not be calculated as no PK blood samples were analysed due to the early termination of the study.

0 minutes (min), 10min, 20min, 40min, 1 hour (h), 1h 30min, 2h, 3h, 4h, 6h, 8h, 10h, 12h and 24h after first drug administration
AUCt,ss (Area Under the Concentration-time Curve of the Analyte in Plasma at Steady State Over a Uniform Dosing Interval t)
Délai: 312 hours (h), 312 h 10 minutes (min), 312h 20min, 312h 40min, 313, 313h 30min, 314h, 315h, 316h, 318h, 320h, 322h, 324h and 336h after first drug administration

AUCt,ss (area under the concentration-time curve of the analyte in plasma at steady state over a uniform dosing interval t).

This endpoint could not be calculated as no PK blood samples were analysed due to the early termination of the study.

312 hours (h), 312 h 10 minutes (min), 312h 20min, 312h 40min, 313, 313h 30min, 314h, 315h, 316h, 318h, 320h, 322h, 324h and 336h after first drug administration
Cmax,ss (Maximum Measured Concentration of the Analyte in Plasma at Steady State Over a Uniform Dosing Interval t)
Délai: 312 hours (h), 312 h 10 minutes (min), 312h 20min, 312h 40min, 313, 313h 30min, 314h, 315h, 316h, 318h, 320h, 322h, 324h and 336h after first drug administration

Cmax,ss (maximum measured concentration of the analyte in plasma at steady state over a uniform dosing interval t).

This endpoint could not be calculated as no PK blood samples were analysed due to the early termination of the study.

312 hours (h), 312 h 10 minutes (min), 312h 20min, 312h 40min, 313, 313h 30min, 314h, 315h, 316h, 318h, 320h, 322h, 324h and 336h after first drug administration

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 mai 2014

Achèvement primaire (Réel)

1 juillet 2014

Achèvement de l'étude (Réel)

1 août 2014

Dates d'inscription aux études

Première soumission

19 mai 2014

Première soumission répondant aux critères de contrôle qualité

23 mai 2014

Première publication (Estimation)

28 mai 2014

Mises à jour des dossiers d'étude

Dernière mise à jour publiée (Estimation)

29 février 2016

Dernière mise à jour soumise répondant aux critères de contrôle qualité

1 février 2016

Dernière vérification

1 février 2016

Plus d'information

Termes liés à cette étude

Autres numéros d'identification d'étude

  • 1334.2
  • 2013-003813-17 (Numéro EudraCT: EudraCT)

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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