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- Ensayo clínico NCT02259959
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
Estado
Terminado
Condiciones
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
Sí
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
Términos relacionados con este estudio
Términos MeSH relevantes adicionales
- Efectos fisiológicos de las drogas
- Agentes neurotransmisores
- Mecanismos moleculares de acción farmacológica
- Parasimpaticolíticos
- Agentes Autonómicos
- Agentes del sistema nervioso periférico
- Antagonistas colinérgicos
- Agentes colinérgicos
- Agentes broncodilatadores
- Agentes antiasmáticos
- Agentes del sistema respiratorio
- Soluciones farmacéuticas
- Bromuro de tiotropio
- Olodaterol
Otros números de identificación del estudio
- 1237.2
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. .