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Pharmacokinetic Properties of Two Dosages Nevirapine Extended Release (XR) Formulations Compared to VIRAMUNE® Tablet as Well as to Nevirapine XR Tablet in Healthy Male Volunteers

11 de julio de 2014 actualizado por: Boehringer Ingelheim

An Open-label, Non-randomised, Single-dose, Parallel-group Study of Pharmacokinetic Properties of 200 mg (2 x 100 mg Tablets Once Daily) and 300 mg (3 x 100 mg Tablets Once Daily) Nevirapine Extended Release Formulations Compared to 200 mg VIRAMUNE® Tablet as Well as to 400 mg Nevirapine Extended Release Tablet Following Oral Administration in Healthy Male Volunteers

Study to determine the pharmacokinetic properties of 200 mg (2 x 100 mg tablets once daily) and 300 mg (3 x 100 mg tablets once daily) Nevirapine extended release formulations and to estimate relative bioavailability of these formulations as compared to 200 mg VIRAMUNE® tablet as well as to 400 mg Nevirapine extended release tablet

Descripción general del estudio

Tipo de estudio

Intervencionista

Inscripción (Actual)

96

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 60 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; values within normal ranges or deviating from normal without clinical relevance as considered by the investigator
  • Values of Liver Function Test (LFT) have to be within normal ranges
  • Age ≥18 and Age ≤60 years
  • Body Mass Index (BMI) ≥18.5 and BMI ≤29.9 kg/m2
  • Subjects must agree to minimize the risk of female partners becoming pregnant from the first dosing day until 3 months after the completion of the post study medical examination. Acceptable methods of contraception comprises barrier contraception and a medically accepted contraceptive method for the female partner (intra-uterine device with spermicide, hormonal contraceptive since at least two month)
  • 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) deviating from normal and of clinical relevance
  • Any evidence of a clinically relevant concomitant disease
  • Gastrointestinal, hepatic, renal, respiratory, cardiovascular, metabolic, immunological or hormonal disorders of clinical relevance
  • Surgery of the gastrointestinal tract (except appendectomy and herniotomy)
  • 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 drug or its excipients)
  • Intake of drugs with a long half-life (>24 hours) within at least one month or less than 10 half-lives of the respective drug prior to administration or during the trial
  • 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 administration or during the trial
  • Participation in another trial with an investigational drug within two months prior to administration or during the trial
  • Participation to trial BI 1100.1485 or any other intake of Nevirapine
  • Smoker (>10 cigarettes or >3 cigars or >3 pipes/day)
  • Inability to refrain from smoking on trial days
  • Alcohol abuse (more than 60 g/day)
  • Drug abuse
  • Blood donation (more than 100 mL within four weeks prior to administration or during the trial)
  • Excessive physical activities (within one week prior to administration or during the trial)
  • Any laboratory value outside the reference range that is of clinical relevance
  • Inability to comply with dietary regimen of trial site
  • A marked baseline prolongation of QT/QTc interval (e.g., repeated demonstration of a QTc interval >450 ms)
  • A history of additional risk factors for Torsades des Pointes (e.g., heart failure, hypokalemia, family history of Long QT Syndrome)
  • History of disease which affects the present situation
  • Inability to understand the protocol requirements, instructions and study-related restrictions, the nature, scope, and possible consequences of the study
  • Unlikely to comply with the protocol requirements, instructions and study-related restrictions; e.g., uncooperative attitude, inability to return for follow-up visits, and improbability of completing the study
  • Subject is the investigator or any sub-investigator, research assistant, pharmacist, study coordinator, other staff or relative thereof directly involved in the conduct of the study
  • Vulnerable subjects (e.g. persons kept in detention)

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: No aleatorizado
  • Modelo Intervencionista: Asignación paralela
  • Enmascaramiento: Ninguno (etiqueta abierta)

Armas e Intervenciones

Grupo de participantes/brazo
Intervención / Tratamiento
Experimental: Nevirapine XR low dose
Experimental: Nevirapine XR medium dose
Comparador activo: Nevirapine XR high dose
Comparador activo: Nevirapine (VIRAMUNE®)
commercial product

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Periodo de tiempo
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 144 hours after drug administration
up to 144 hours after drug administration
Cmax (maximum measured concentration of the analyte in plasma)
Periodo de tiempo: up to 144 hours after drug administration
up to 144 hours after drug administration

Medidas de resultado secundarias

Medida de resultado
Periodo de tiempo
Número de pacientes con eventos adversos
Periodo de tiempo: hasta 36 días
hasta 36 días
λz (constante de velocidad terminal en plasma)
Periodo de tiempo: hasta 144 horas después de la administración del fármaco
hasta 144 horas después de la administración del fármaco
AUC0-tz (area under the concentration-time curve of the analyte in plasma over the time interval from 0 to the time of the last quantifiable data point)
Periodo de tiempo: up to 144 hours after drug administration
up to 144 hours after drug administration
tmax (time from dosing to the maximum concentration of the analyte in plasma)
Periodo de tiempo: up to 144 hours after drug administration
up to 144 hours after drug administration
t1/2 (terminal half-life of the analyte in plasma)
Periodo de tiempo: up to 144 hours after drug administration
up to 144 hours after drug administration
MRTpo (mean residence time of the analyte in the body after po administration)
Periodo de tiempo: up to 144 hours after drug administration
up to 144 hours after drug administration
CL/F (apparent clearance of the analyte in the plasma after extravascular administration)
Periodo de tiempo: up to 144 hours after drug administration
up to 144 hours after drug administration
Vz/F (apparent volume of distribution during the terminal phase λz following an extravascular dose)
Periodo de tiempo: up to 144 hours after drug administration
up to 144 hours after drug administration
ka (absorption rate constant)
Periodo de tiempo: up to 144 hours after drug administration
up to 144 hours after drug administration
Number of patients with abnormal changes in laboratory parameters
Periodo de tiempo: Screening, Day 1, 2, 3, 4, 5, 7, 15
Screening, Day 1, 2, 3, 4, 5, 7, 15
Number of patients with clinically significant changes in vital signs (blood pressure (BP), pulse rate (PR))
Periodo de tiempo: Screening, Day 1, 2, 15
Screening, Day 1, 2, 15
Number of patients with clinically significant changes in 12-lead electrocardiogram (ECG)
Periodo de tiempo: Screening, Day 1, 15
Screening, Day 1, 15
Assessment of tolerability by investigator on a 4-point scale
Periodo de tiempo: up to 15 days after drug administration
up to 15 days after 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 abril de 2008

Finalización primaria (Actual)

1 de julio de 2008

Fechas de registro del estudio

Enviado por primera vez

8 de julio de 2014

Primero enviado que cumplió con los criterios de control de calidad

8 de julio de 2014

Publicado por primera vez (Estimar)

9 de julio de 2014

Actualizaciones de registros de estudio

Última actualización publicada (Estimar)

14 de julio de 2014

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

11 de julio de 2014

Última verificación

1 de julio 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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