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High-Dose PEG-Intron Pharmacokinetic Study in Patients With Melanoma (Study P04831 AM2)

15 de mayo de 2017 actualizado por: Merck Sharp & Dohme LLC

A Pharmacokinetic Study of PEG-Intron, Administered Weekly in Subjects With High-Risk Melanoma

The purpose of this study is to establish the pharmacokinetics of PEG-Intron, administered at a dose of 6 μg/kg/week for 8 weeks (induction treatment), followed by a dose of 3 μg/kg/week for up to 252 weeks (maintenance treatment), in patients with high risk melanoma.

Descripción general del estudio

Estado

Terminado

Condiciones

Intervención / Tratamiento

Tipo de estudio

Intervencionista

Inscripción (Actual)

32

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 y mayores (Adulto, Adulto Mayor)

Acepta Voluntarios Saludables

No

Géneros elegibles para el estudio

Todos

Descripción

Inclusion Criteria:

  • Subjects at least 18 years of age, of either sex, and of any race.
  • Cytologically or histologically-confirmed melanoma, arising from a cutaneous or unknown site of origin, at Stages IIB, IIC, IIIA, IIIB, IIIC according to the American Joint Committee on Cancer (AJCC) 2001 guidelines.
  • Adequate hepatic, renal and bone marrow function within 4 weeks prior to initiation of study treatment.
  • Subjects presenting with synchronous primary and regional melanoma must have had adequate surgical margins surrounding the primary lesion.
  • Full lymphadenectomy must be performed within 90 days prior to initiation of study treatment.
  • Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1.
  • Give informed consent according to International Conference on Harmonisation - Good Clinical Practice (ICH-GCP) and national/local policy.
  • Be able to adhere to dose and visit schedules.
  • Female subjects of childbearing potential must be using a medically accepted method of birth control prior to Screening and agree to continue its use during the study or be surgically sterilized.
  • Female subjects of childbearing potential must have a negative serum pregnancy test at Screening.

Exclusion Criteria:

  • Female subjects who are pregnant, intend to become pregnant, or are breastfeeding.
  • Previous treatment with interferon alpha, chemotherapy or immunotherapy for melanoma.
  • Ocular melanoma, or melanoma of the mucous membranes.
  • Evidence of distant or non-regional lymph node metastases.
  • In-transit melanoma, even if the lesion has been resected.
  • Disease that cannot be completely surgically resected.
  • Lack of recovery from recent surgery.
  • Prior malignancy within the past 5 years, except surgically cured squamous cell carcinoma of the skin, successfully resected early stage cutaneous melanoma, or cervical carcinoma in situ.
  • Severe cardiovascular disease.
  • Thyroid dysfunction not responsive to therapy.
  • Uncontrolled diabetes mellitus (in the opinion of the investigator).
  • Active autoimmune disease.
  • Active and/or uncontrolled infection.
  • History of seropositivity for human immunodeficiency virus (HIV).
  • Pre-existing psychiatric condition.
  • Clinical diagnosis of substance abuse of one or more of the following drugs within the following timeframes (excluding time spent in detoxification, hospitalization or incarceration):

    • Alcohol, intravenous drug use, inhalational, psychotropics, narcotics, cocaine, prescription or over-the-counter drugs: within 1 year of the Screening visit.
    • Methadone, buprenorphine hydrochloride (HCl), and/or butorphanol tartrate: within 1 year of Screening visit, unless subject has drug screen negative for other (non-narcotic) drugs documented in the past year and repeated negative within 2 months of Screening visit.
    • Multi-drug abuse (2 or more substances in 16a and 16b): within 3 years of Screening visit.
    • Marijuana:

      • If historic use is deemed excessive by the principal investigator (or medically qualified individual), or is interfering with the subject's life, then the subject is not eligible and should not be screened.
      • If marijuana use is not deemed excessive by principal investigator and does not interfere with life, subject must discontinue any current use of marijuana prior to entry into study.
  • Medical condition requiring chronic systemic corticosteroids.
  • Known allergy to the drug substance or any of the excipients in the PEG-Intron formulation.
  • Any situation or condition that, in the opinion of the investigator, may interfere with optimal participation in the study.
  • Use of any investigational drugs within 30 days of study entry.
  • Participation in other clinical studies of investigational treatments.

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 de un solo grupo
  • Enmascaramiento: Ninguno (etiqueta abierta)

Armas e Intervenciones

Grupo de participantes/brazo
Intervención / Tratamiento
Experimental: PEG-Intron

6 ug/kg/week, SC (first 8 weeks)

3 ug/kg/week, SC (252 weeks [weeks 9-260], maintenance)

Otros nombres:
  • SCH 054031
  • peginterferón alfa-2b

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Area Under the Curve (AUC) of PEG-Intron at 12 Weeks
Periodo de tiempo: Predose, and 24, 48, 72, 96, and 168 hours postdose at 12 weeks
AUC was defined as the actual body exposure to drug after administration of a dose of the drug.
Predose, and 24, 48, 72, 96, and 168 hours postdose at 12 weeks
Maximum Serum Concentration (Cmax) of PEG-Intron at 12 Weeks
Periodo de tiempo: Predose, and 24, 48, 72, 96, and 168 hours postdose at 12 weeks
Cmax was defined as observed maximum plasma concentration.
Predose, and 24, 48, 72, 96, and 168 hours postdose at 12 weeks
Average Concentration Within the Dosing Interval (Cavg) of PEG-Intron at 12 Weeks
Periodo de tiempo: Predose, and 24, 48, 72, 96, and 168 hours postdose at 12 weeks
Cavg was defined as average plasma concentration.
Predose, and 24, 48, 72, 96, and 168 hours postdose at 12 weeks
Minimum Serum Concentration (Cmin) of PEG-Intron at 12 Weeks
Periodo de tiempo: Predose, and 24, 48, 72, 96, and 168 hours postdose at 12 weeks
Cmin was defined as observed minimum plasma concentration.
Predose, and 24, 48, 72, 96, and 168 hours postdose at 12 weeks
Observed Time to Achieve Cmax (Tmax) of PEG-Intron at 12 Weeks
Periodo de tiempo: Predose, and 24, 48, 72, 96, and 168 hours postdose at 12 weeks
Tmax was defined as time of maximum plasma concentration.
Predose, and 24, 48, 72, 96, and 168 hours postdose at 12 weeks
Apparent Clearance(CL/F) of PEG-Intron at 12 Weeks
Periodo de tiempo: Predose, and 24, 48, 72, 96, and 168 hours postdose at 12 weeks
CL/F was defined apparent clearance - the volume of plasma in the vascular compartment cleared of drug per unit of time and per kilogram of body weight by the processes of metabolism and excretion.
Predose, and 24, 48, 72, 96, and 168 hours postdose at 12 weeks

Medidas de resultado secundarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Number of Participants Who Experienced an Adverse Event (AE)
Periodo de tiempo: Entire study duration (up to 5 years)
An adverse event (AE) was defined as any untoward medical occurrence or unfavorable and unintended sign in a subject administered a pharmaceutical product, biologic (at any dose), or medical device, whether or not considered related to the use of that product.
Entire study duration (up to 5 years)

Colaboradores e Investigadores

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

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.

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 (Actual)

20 de febrero de 2007

Finalización primaria (Actual)

27 de mayo de 2008

Finalización del estudio (Actual)

11 de julio de 2012

Fechas de registro del estudio

Enviado por primera vez

5 de abril de 2007

Primero enviado que cumplió con los criterios de control de calidad

5 de abril de 2007

Publicado por primera vez (Estimar)

6 de abril de 2007

Actualizaciones de registros de estudio

Última actualización publicada (Actual)

7 de junio de 2017

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

15 de mayo de 2017

Última verificación

1 de mayo de 2017

Más información

Términos relacionados con este estudio

Plan de datos de participantes individuales (IPD)

¿Planea compartir datos de participantes individuales (IPD)?

Descripción del plan IPD

http://www.merck.com/clinical-trials/pdf/Merck%20Procedure%20on%20Clinical%20Trial%20Data%20Access%20Final_Updated%20July_9_2014.pdf

http://engagezone.msd.com/ds_documentation.php

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 PEG-Intron

3
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