- ICH GCP
- Registro de ensayos clínicos de EE. UU.
- Ensayo clínico NCT02409004
Effects of Rifampin on the Pharmacokinetics of Ataluren
A Phase I Study Assessing the Effects of Rifampin on the Pharmacokinetics of Ataluren in Healthy Subjects
Descripción general del estudio
Descripción detallada
A total of 15 healthy, adult, male non-smokers, were included in this study. Subjects were administered ataluren on Day 1 followed by rifampin from Days 3 to12, and again ataluren on Day 11. On Day 11, ataluren was administered before rifampin administration.
Prior to entering the trial, subjects had a screening visit to establish eligibility within 28 days before study drug administration. Subjects were confined from at least10 hours before the first ataluren dosing on Day 1 until approximately 50 hours postdose(Day 3). Thereafter, subjects came back every morning from Days 4 to 10 for rifampin dosing. Then, subjects reported to the clinical site at least 10 hours before ataluren dosing on Day 11 (evening of Day 10) and remained in the clinical site until after 50 hours post-Day 11 ataluren dose (Day 13).
Tipo de estudio
Inscripción (Actual)
Fase
- Fase 1
Contactos y Ubicaciones
Ubicaciones de estudio
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Quebec, Canadá, G1P 0A2
- inVentiv
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Criterios de participación
Criterio de elegibilidad
Edades elegibles para estudiar
Acepta Voluntarios Saludables
Géneros elegibles para el estudio
Descripción
Inclusion Criteria:
- Male, non-smoker (no use of tobacco products within two years prior to screening), ≥18 and ≤55 years of age, with Body Mass Index (BMI) >20.0 and <30.0 kg/m2 and body weight ≥50.0 kg.
Healthy as defined by:
- the absence of clinically significant illness and surgery within four weeks prior to dosing. Subjects vomiting within 24 hours pre-first dose of ataluren will be carefully evaluated for upcoming illness/disease. Inclusion pre-dosing is at the discretion of the QI;
- the absence of clinically significant history of neurological, endocrinal, cardiovascular, pulmonary, hematological, immunologic, psychiatric, gastrointestinal, renal, hepatic, and metabolic disease;
- the absence of any known nonsense mutation-mediated disease including Duchenne Muscular Dystrophy.
- Capable of consent.
- Willing to take off dentures at dosing.
- Consent to perform genotyping for UGT1A9
Exclusion Criteria:
- Any clinically significant abnormality or abnormal laboratory test results found during medical screening or positive test for hepatitis B, hepatitis C, or HIV found during medical screening.
- Positive urine drug screen or urine cotinine test at screening.
- History of allergic reactions to ataluren, rifampin, or other related drugs.
- Use of any drugs known to induce or inhibit hepatic drug metabolism within 30 days prior to the first study drug administration.
- Any reason which, in the opinion of the QI, would prevent the subject from participating in the study.
- Clinically significant electrocardiogram (ECG) abnormalities or vital sign abnormalities (systolic blood pressure lower than 90 or over 140 mmHg, diastolic blood pressure lower than 50 or over 90 mmHg, or heart rate less than 50 or over 100 bpm) at screening.
- History of significant alcohol abuse within one year prior to screening or regular use of alcohol within six months prior to the screening visit (more than 14 units of alcohol per week [1 unit = 150 mL of wine, 360 mL of beer, or 45 mL of 40% alcohol]).
- History of significant drug abuse within one year prior to screening or use of soft drugs (such as marijuana) within three months prior to the screening visit or hard drugs (such as cocaine, phencyclidine [PCP], and crack) within one year prior to screening.
- Participation in a clinical trial involving the administration of an investigational or marketed drug within 30 days (90 days for biologics) prior to the first dosing or concomitant participation in an investigational study involving no drug administration.
Use of medication other than topical products without significant systemic absorption:
- prescription medication within 14 days prior to the first dosing;
- over-the-counter products including natural health products (eg, food supplements and herbal supplements) within seven days prior to the first ataluren dosing, with the exception of the occasional use of acetaminophen (up to 2 g daily);
- a depot injection or an implant of any drug within three months prior to the first dosing.
- Donation of plasma within seven days prior to dosing. Donation or loss of blood (excluding volume drawn at screening) of 50 mL to 499 mL of blood within 30 days, or more than 499 mL within 56 days prior to the first dosing.
- Hemoglobin <128 g/L and hematocrit <0.37 L/L at screening.
Plan de estudios
¿Cómo está diseñado el estudio?
Detalles de diseño
- Propósito principal: Tratamiento
- Asignación: N / A
- Modelo Intervencionista: Asignación de un solo grupo
- Enmascaramiento: Ninguno (etiqueta abierta)
Armas e Intervenciones
Grupo de participantes/brazo |
Intervención / Tratamiento |
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Experimental: Ataluren
Ataluren 1375 mg powder for oral suspension administered once daily on Days 1 and 11 Rifampin 300 mg capsules administered twice daily on Day 3 to Day 12
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Powder for oral suspension (supplied in sachets) 1X 125 mg + 1 x 250 mg + 1000 mg (total of 1375 mg)
Otros nombres:
Capsule 2x3oo mg Oral
Otros nombres:
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¿Qué mide el estudio?
Medidas de resultado primarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
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Area under the plasma concentration versus time curve (AUC)
Periodo de tiempo: 12 days
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The objective of this study is to determine the effects of rifampin on the pharmacokinetics of ataluren under fasting conditions.
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12 days
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Maximum plasma concentration (Cmax)
Periodo de tiempo: 12 days
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The objective of this study is to determine the effects of rifampin on the pharmacokinetics of ataluren under fasting conditions.
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12 days
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Medidas de resultado secundarias
Medida de resultado |
Periodo de tiempo |
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Safety as measured by adverse events, laboratory abnormalities, vital signs, and electrocardiogram parameters
Periodo de tiempo: 12 days
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12 days
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Colaboradores e Investigadores
Patrocinador
Investigadores
- Director de estudio: Oscar Laskin, MD, PTC Therapeutics
Fechas de registro del estudio
Fechas importantes del estudio
Inicio del estudio
Finalización primaria (Actual)
Finalización del estudio (Actual)
Fechas de registro del estudio
Enviado por primera vez
Primero enviado que cumplió con los criterios de control de calidad
Publicado por primera vez (Estimar)
Actualizaciones de registros de estudio
Última actualización publicada (Actual)
Última actualización enviada que cumplió con los criterios de control de calidad
Última verificación
Más información
Términos relacionados con este estudio
Palabras clave
Términos MeSH relevantes adicionales
- Mecanismos moleculares de acción farmacológica
- Agentes antiinfecciosos
- Inhibidores de la síntesis de ácidos nucleicos
- Inhibidores de enzimas
- Agentes antibacterianos
- Agentes leprostáticos
- Inductores de enzimas de citocromo P-450
- Inductores de citocromo P-450 CYP3A
- Agentes antituberculosos
- Antibióticos, Antituberculosos
- Inductores de citocromo P-450 CYP2B6
- Inductores de citocromo P-450 CYP2C8
- Inductores del citocromo P-450 CYP2C19
- Inductores de citocromo P-450 CYP2C9
- Rifampicina
Otros números de identificación del estudio
- PTC124-GD-026-HV
Plan de datos de participantes individuales (IPD)
¿Planea compartir datos de participantes individuales (IPD)?
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. .
Ensayos clínicos sobre Ataluren
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PTC TherapeuticsTerminadoEnfermedades del Sistema Nervioso | Enfermedades Genéticas Congénitas | Enfermedades Genéticas, Ligadas al X | Enfermedades Musculares | Enfermedades Neuromusculares | Distrofias Musculares | Trastornos Musculares Atróficos | Distrofia Muscular, Duchenne | Enfermedad musculoesqueléticaEstados Unidos, Taiwán, India, Tailandia, Australia, Brasil, Bulgaria, Canadá, Porcelana, Hong Kong, Malasia, México, Puerto Rico, Polonia, Japón, Corea del Sur, Rusia, Turquía (Türkiye)
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PTC TherapeuticsTerminadoUn estudio para evaluar la seguridad y la farmacocinética de ataluren en participantes de ≥6 meses aDistrofia muscular de Duchenne con mutación sin sentidoEstados Unidos
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PTC TherapeuticsTerminadoDistrofia muscular de DuchenneEstados Unidos
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PTC TherapeuticsTerminado
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PTC TherapeuticsTerminadoFibrosis quísticaEstados Unidos, Francia, España, Bélgica, Israel, Italia, Suecia
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PTC TherapeuticsTerminadoFibrosis quísticaFrancia, Bélgica
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PTC TherapeuticsRetirado
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PTC TherapeuticsCystic Fibrosis FoundationTerminadoFibrosis quísticaEstados Unidos, Francia, Bélgica, España, Canadá, Alemania, Israel, Italia, Países Bajos, Suecia, Reino Unido
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PTC TherapeuticsTerminadoEnfermedades del Sistema Nervioso | Enfermedades Genéticas Congénitas | Enfermedades Genéticas, Ligadas al X | Enfermedades musculoesqueléticas | Enfermedades Musculares | Enfermedades Neuromusculares | Distrofias Musculares | Trastornos Musculares Atróficos | Distrofia Muscular, DuchenneEstados Unidos, España, Corea, república de, Bélgica, Francia, Canadá, Australia, Reino Unido, Israel, Italia, Alemania, Brasil, Bulgaria, Chile, Chequia, Polonia, Suecia, Suiza, Pavo
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PTC TherapeuticsGenzyme, a Sanofi CompanyTerminadoMetabolismo de aminoácidos, errores congénitosFrancia, Reino Unido, Italia, Bélgica, Alemania, Suiza