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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 de octubre de 2014 actualizado por: 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

Descripción general del estudio

Tipo de estudio

Intervencionista

Inscripción (Actual)

36

Fase

  • Fase 1

Criterios de participación

Los investigadores buscan personas que se ajusten a una determinada descripción, denominada criterio de elegibilidad. Algunos ejemplos de estos criterios son el estado de salud general de una persona o tratamientos previos.

Criterio de elegibilidad

Edades elegibles para estudiar

21 años a 45 años (Adulto)

Acepta Voluntarios Saludables

Géneros elegibles para el estudio

Masculino

Descripción

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 de estudios

Esta sección proporciona detalles del plan de estudio, incluido cómo está diseñado el estudio y qué mide el estudio.

¿Cómo está diseñado el estudio?

Detalles de diseño

  • Propósito principal: Tratamiento
  • Asignación: Aleatorizado
  • Modelo Intervencionista: Asignación paralela
  • Enmascaramiento: Doble

Armas e Intervenciones

Grupo de participantes/brazo
Intervención / Tratamiento
Comparador de placebos: Placebo
Experimental: BI 1744 CL in combination with Tiotropium

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Number of subjects with clinically relevant findings in physical examination
Periodo de tiempo: Up to day 32
Up to day 32
Number of subjects with clinically relevant findings in vital signs
Periodo de tiempo: Up to day 32
blood pressure, pulse rate
Up to day 32
Number of subjects with clinically relevant findings in 12-lead ECG
Periodo de tiempo: Up to day 32
Up to day 32
Number of subjects with clinically relevant findings in laboratory tests
Periodo de tiempo: Up to day 32
Up to day 32
Number of subjects witch clinically relevant changes in additional safety laboratory test parameters
Periodo de tiempo: 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
Periodo de tiempo: 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
Periodo de tiempo: Up to day 32
Up to day 32
Global assessment of tolerability by investigator on a 4-point scale
Periodo de tiempo: Up to day 32
Up to day 32

Medidas de resultado secundarias

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

Colaboradores e Investigadores

Aquí es donde encontrará personas y organizaciones involucradas en este estudio.

Patrocinador

Publicaciones y enlaces útiles

La persona responsable de ingresar información sobre el estudio proporciona voluntariamente estas publicaciones. Estos pueden ser sobre cualquier cosa relacionada con el estudio.

Enlaces Útiles

Fechas de registro del estudio

Estas fechas rastrean el progreso del registro del estudio y los envíos de resultados resumidos a ClinicalTrials.gov. Los registros del estudio y los resultados informados son revisados ​​por la Biblioteca Nacional de Medicina (NLM) para asegurarse de que cumplan con los estándares de control de calidad específicos antes de publicarlos en el sitio web público.

Fechas importantes del estudio

Inicio del estudio

1 de abril de 2007

Finalización primaria (Actual)

1 de septiembre de 2007

Fechas de registro del estudio

Enviado por primera vez

7 de octubre de 2014

Primero enviado que cumplió con los criterios de control de calidad

7 de octubre de 2014

Publicado por primera vez (Estimar)

9 de octubre de 2014

Actualizaciones de registros de estudio

Última actualización publicada (Estimar)

9 de octubre de 2014

Última actualización enviada que cumplió con los criterios de control de calidad

7 de octubre de 2014

Última verificación

1 de octubre de 2014

Más información

Esta información se obtuvo directamente del sitio web clinicaltrials.gov sin cambios. Si tiene alguna solicitud para cambiar, eliminar o actualizar los detalles de su estudio, comuníquese con register@clinicaltrials.gov. Tan pronto como se implemente un cambio en clinicaltrials.gov, también se actualizará automáticamente en nuestro sitio web. .

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