- ICH GCP
- Registro de ensayos clínicos de EE. UU.
- Ensayo clínico NCT02256787
Safety, Tolerance, and Pharmacokinetics of Single Rising Oral Doses of BILB 1941 ZW Solution in Healthy Male Subjects, Followed With Bioavailability Comparison of BILB 1941 ZW Tablet and Solution Formulation Administered With or Without Food
2 de octubre de 2014 actualizado por: Boehringer Ingelheim
Safety, Tolerance, and Pharmacokinetics of Single Oral Doses of 5 mg, 20 mg, 60 mg, 120 mg, 200 mg, 300 mg, 600 mg, 1000 mg, 1500 mg, 2000 mg, 2400 mg, and 3000 mg BILB 1941 ZW (PEG 400/TRIS Solution) in Healthy Male Subjects, in a Randomised Double Blind, Placebo Controlled Rising Dose Study, Followed With an Open-label Intra-subject Three-Way Crossover Bioavailability Comparison of 600 mg BILB 1941 ZW in a PEG 400/TRIS Solution and 600 mg BILB 1941 ZW Tablet and 600 mg BILB 1941 ZW Tablet Administered With Food
The objective of the current study was to investigate the safety, tolerability, and pharmacokinetics of BILB 1941 ZW following the administration of single rising doses from 5 mg to 300 mg.
In addition the bioavailability of the 60 mg dose given fasted and after a high-fat breakfast was to be be investigated
Descripción general del estudio
Estado
Terminado
Condiciones
Tipo de estudio
Intervencionista
Inscripción (Actual)
56
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
18 años a 50 años (Adulto)
Acepta Voluntarios Saludables
Sí
Géneros elegibles para el estudio
Masculino
Descripción
Inclusion Criteria:
Healthy males according to the following criteria based upon a complete medical history, including the physical examination, vital signs (BP, PR), 12-lead ECG, clinical laboratory tests:
1.1 No finding deviating from normal and of clinical relevance
1.2 No evidence of a clinically relevant concomitant disease
- Age ≥18 and Age ≤50 years, BMI ≥18.5 and BMI ≤29.9 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 blood pressure, pulse rate and ECG) deviating from normal and of clinical relevance
- History or current gastrointestinal, hepatic, renal, respiratory, cardiovascular, metabolic, immunologic, hormonal disorders, including a clinical history of viral hepatitis, or serological evidence of active Hepatitis B or Hepatitis C infection
- History of orthostatic hypotension, fainting spells and blackouts
- Diseases of the central nervous system (such as epilepsy) or psychiatric disorders or neurological disorders
- Chronic or relevant acute infections
- History of allergy/hypersensitivity (including drug allergy) which is deemed relevant to the trial as judged by the investigator
- Intake of drugs with a long half-life (> 24 hours) within 1 month prior to administration
- Use of any drugs which might influence the results of the trial within 10 days prior to administration or during the trial
- Participation in another trial with an investigational drug within 1 month prior to administration or during the trial
- Smoker (> 10 cigarettes or 3 cigars or 3 pipes/day) or inability to refrain from smoking on trial days
- Alcohol abuse (> 60 g/day)
- Drug abuse
- Blood donation of more than 100 mL within 1 month prior to administration or during the trial
- Excessive physical activities within 5 days prior to administration or during the trial
- Any laboratory value outside the clinically accepted reference range and of clinical relevance
- History of any familial bleeding disorder
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 |
|---|---|
|
Experimental: BILB 1941 ZW - single rising dose
Single rising dose part
|
|
|
Comparador de placebos: Placebo
Single rising dose part
|
|
|
Experimental: BILB 1941 ZW - tablet - fasted
Relative bioavailability: The oral solution fasted should be compared with the solid form fasted and after a standardized breakfast
|
|
|
Experimental: BILB 1941 ZW - solution
Relative bioavailability: The oral solution fasted should be compared with the solid form fasted and after a standardized breakfast
|
|
|
Experimental: BILB 1941 ZW - tablet - fed
Relative bioavailability: The oral solution fasted should be compared with the solid form fasted and after a standardized breakfast
|
¿Qué mide el estudio?
Medidas de resultado primarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
|
Number of subjects with abnormal findings in physical examination
Periodo de tiempo: up to 48 hours following drug administration
|
up to 48 hours following drug administration
|
|
|
Number of subjects with abnormal changes in laboratory parameters
Periodo de tiempo: up to 48 hours following drug administration
|
up to 48 hours following drug administration
|
|
|
Number of subjects with clinically significant changes in vital signs
Periodo de tiempo: up to 48 hours following drug administration
|
Blood pressure, Pulse Rate
|
up to 48 hours following drug administration
|
|
Number of subjects with adverse events
Periodo de tiempo: up to 48 hours following drug administration
|
up to 48 hours following drug administration
|
|
|
Number of subjects with clinically significant changes in 12-lead ECG (electrocardiogram)
Periodo de tiempo: up to 48 hours following drug administration
|
up to 48 hours following drug administration
|
|
|
Assessment of tolerability by investigator on a 4-point scale
Periodo de tiempo: after 48 hours following drug administration
|
after 48 hours following drug administration
|
Medidas de resultado secundarias
Medida de resultado |
Periodo de tiempo |
|---|---|
|
Cmax (maximum concentration of the analyte in plasma)
Periodo de tiempo: up to 48 hours following drug administration
|
up to 48 hours following drug administration
|
|
tmax (time from dosing to maximum concentration)
Periodo de tiempo: up to 48 hours following drug administration
|
up to 48 hours following drug administration
|
|
AUC0-∞ (area under the concentration time curve of the analyte in plasma over the time interval from 0 extrapolated to infinity)
Periodo de tiempo: up to 48 hours following drug administration
|
up to 48 hours following drug administration
|
|
AUC0-tz (area under the concentration-time curve of the analyte in plasma over the time interval from 0 to the last quantifiable data point)
Periodo de tiempo: up to 48 hours following drug administration
|
up to 48 hours following drug administration
|
|
λz (terminal rate constant in plasma)
Periodo de tiempo: up to 48 hours following drug administration
|
up to 48 hours following drug administration
|
|
t1/2 (terminal half-life of the analyte in plasma)
Periodo de tiempo: up to 48 hours following drug administration
|
up to 48 hours following drug administration
|
|
MRT (Mean time of residence of drug molecules in the body after intravascular administration)
Periodo de tiempo: up to 48 hours following drug administration
|
up to 48 hours following drug administration
|
|
Vz/F (Apparent volume of distribution during the terminal phase after extravascular administration)
Periodo de tiempo: up to 48 hours following drug administration
|
up to 48 hours following drug administration
|
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 enero de 2004
Finalización primaria (Actual)
1 de septiembre de 2004
Fechas de registro del estudio
Enviado por primera vez
2 de octubre de 2014
Primero enviado que cumplió con los criterios de control de calidad
2 de octubre de 2014
Publicado por primera vez (Estimar)
6 de octubre de 2014
Actualizaciones de registros de estudio
Última actualización publicada (Estimar)
6 de octubre de 2014
Última actualización enviada que cumplió con los criterios de control de calidad
2 de octubre de 2014
Última verificación
1 de octubre de 2014
Más información
Términos relacionados con este estudio
Otros números de identificación del estudio
- 1201.1
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. .