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A Leukapheresis Study for Immune Responses in Healthy US Adults Who Receive BCG Vaccination Followed by Boosting With AERAS-402 (C-021-402)

27 de febrero de 2015 actualizado por: Aeras

A Phase I, Double-Blind, Randomized, Placebo-controlled Leukapheresis Study to Obtain Lymphocytes for the Study of Immune Responses in Healthy Adult Volunteers in the U.S. Who Receive BCG Vaccination Followed by Boosting With AERAS-402

Healthy adults received BCG on Study Day -84, followed by randomization on Study Day 0 to receive 2 booster doses in a blinded fashion of either AERAS-402 (N=9) or placebo (N=2) on Study Days 0 and 28. Subjects were followed for a total of 98 days.

Descripción general del estudio

Descripción detallada

This was a double-blind, randomized, placebo-controlled study. At least 13, but no more than 16, subjects who met all eligibility criteria were to receive a prime vaccination with BCG (1-8 x 105 colony forming units [CFU] intradermally [ID]) at Study Day -84. Thirteen of the BCG-vaccinated subjects who completed all protocol-specified procedures and continued to meet eligibility criteria were to be enrolled and randomized on Study Day 0 in a 10:3 ratio to receive study vaccine (either AERAS-402 3 x 1010 virus particles [vp] intramuscularly [IM] or placebo IM) at Study Days 0 and 28, based on time of completion of screening. Eleven subjects were randomized (N=9 AERAS-402; N=2 placebo) and analyzed. Enrollment was stopped when 11 of the planned 13 subjects had been randomized, as it was felt that this number of subjects was sufficient to address the objectives of the study.

Tipo de estudio

Intervencionista

Inscripción (Actual)

11

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 45 años (Adulto)

Acepta Voluntarios Saludables

Sí

Géneros elegibles para el estudio

Todos

Descripción

Inclusion Criteria:

  1. Is male or female
  2. Provided written informed consent prior to any study related procedures
  3. Is age ≥18 years and ≤45 years on Study Day -84.
  4. Has Body Mass Index (BMI) ≥19 and <33 by nomogram (see appendices)
  5. Has general good health, confirmed by medical history and physical examination
  6. Females physically capable of pregnancy (not sterilized and still menstruating or within 1 year of the last menses if menopausal) in sexual relationships with men must avoid pregnancy with an acceptable method of avoiding pregnancy from 28 days prior to Study Day -84 through the end of the study.
  7. Females physically capable of pregnancy must have a negative serum pregnancy test within 7 days prior to Study Day -84 AND a negative urine pregnancy test on Study Day -84, Study Day 0, and Study Day 28.
  8. Has committed to avoid elective surgery for the duration of the study
  9. Has ability to complete all study visits as required per the protocol and is able to be contacted by telephone

Exclusion Criteria:

  1. Acute illness, oral temperature ≥37.5°C, or axillary lymphadenopathy on Study Day -84, Study Day 0, or Study Day 28.
  2. Any of the following laboratory results from blood and urine collected within 7 days prior to Study Day -84 (evaluated per local laboratory parameters):

    • Abnormal hemoglobin or hematocrit
    • Abnormal white blood cell count, absolute neutrophil count, or absolute lymphocyte count
    • Elevated creatinine, total bilirubin, AST, ALT, or alkaline phosphatase (ALP)
  3. Evidence of chronic hepatitis (e.g., hepatitis B core antibody, or hepatitis C antibody, or other)
  4. Laboratory test (e.g., QuantiFERON®-TB) evidence of Mycobacterium tuberculosis (Mtb) infection
  5. History of residence in a tuberculosis-endemic country, per WHO 2008 "high-burden" definition
  6. History of treatment for active or latent tuberculosis infection
  7. History or evidence (including chest X-ray) of active tuberculosis
  8. Shared a residence within the last year with an individual on anti-tuberculosis treatment or with culture or smear positive tuberculosis
  9. History of allergic disease or reactions likely to be exacerbated by any component of the BCG or study vaccines
  10. History of autoimmune disease or immunosuppression
  11. Current household contact or occupational exposure to an individual with known significant immunosuppression
  12. History or evidence on physical examination of any systemic disease, or acute or chronic illness that, in the opinion of the investigator, may interfere with the evaluation of the safety or immunogenicity of the vaccine, including axillary lymphadenopathy
  13. History or laboratory evidence of any past, present or future possible immunodeficiency state which will include (but is not limited to) any laboratory indication of HIV infection
  14. History of alcohol or drug abuse within the past 2 years
  15. History of cheloid formation
  16. Previous medical history that may compromise the safety of the subject in the study
  17. Any current medical, psychiatric, occupational, or substance abuse problems which, in the opinion of the investigator, will make it unlikely the subject will comply with the protocol
  18. Inability to discontinue daily medications during the study period except the following:

    • Contraceptives
    • Multivitamins
    • Inhaled or topical corticosteroids
  19. Tobacco smoking of a pack or more of cigarettes a day, or cannabis smoking three or more days per week
  20. Received immunosuppressive medication within 45 days prior to Study Day -84 (inhaled and topical corticosteroids are permitted)
  21. Received investigational drugs or vaccine products within 182 days prior to Study Day -84 or planned participation in any other investigational study during the study period
  22. Received investigational Mtb vaccine at any time prior to Study Day -84
  23. Received vaccination or immunotherapy with a BCG product at any time prior to Study Day -84.
  24. Received immunoglobulin or blood products within 45 days prior to Study Day -84.
  25. Received any standard vaccine within 45 days prior to Study Day -84 except inactivated influenza vaccine which may have been received within 2 weeks prior to Study Day -84.
  26. History of high risk sexual behaviors since 1977.

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: Prevención
  • Asignación: Aleatorizado
  • Modelo Intervencionista: Asignación paralela
  • Enmascaramiento: Cuadruplicar

Armas e Intervenciones

Grupo de participantes/brazo
Intervención / Tratamiento
Experimental: AERAS-402
3 x10^10 viral particles per 0.5 mL suspended in 10 mM Tris buffer, 1 mM MgCl2, 75 mM NaCl, 5% w/v sucrose, 0.02% w/v PS-80 (polysorbate-80), 0.1 mM EDTA, 10 mM l-histidine, 0.5% v/v ethanol and water. The dose volume administered was 0.5 mL.
Live recombinant serotype 35 replication deficient adenovirus vector expressing a fusion protein of 3 Mycobacterium tuberculosis antigens (Ag85A, Ag85B, and TB10.4).
BCG given to all participants at day -84 prior to a boost with either Aeras-402 or placebo.
Comparador activo: Placebo
1.0 mL sterile vaccine buffer containing 10mM Tris buffer, 1 mM MgCl2, 75 mM NaCl, 5% w/v sucrose, 0.02% w/v PS-80 (polysorbate-80), 0.1 mM EDTA, 10 mM l-histidine, 0.5% v/v ethanol and water. The dose volume administered was 0.5 mL
BCG given to all participants at day -84 prior to a boost with either Aeras-402 or placebo.
Identical buffer solution in which AERAS-402 is formulated.

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Cellular immune responses to AERAS-402 in healthy adult volunteers who received two booster doses of AERAS-402 administered 84 and 112 days after BCG vaccination, through leukapheresis and cryopreservation of cells followed by in vitro assay.
Periodo de tiempo: Up to study day 98
percentage of CD4 and CD8 T cells from leukapheresis that produce any of three cytokines (IFN γ, TNF α, and/or IL 2).
Up to study day 98

Medidas de resultado secundarias

Medida de resultado
Periodo de tiempo
Evaluation of adverse events (AEs) and serious adverse events (SAEs).
Periodo de tiempo: Up to study day 98
Up to study day 98

Colaboradores e Investigadores

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

Patrocinador

Investigadores

  • Director de estudio: Ann M Ginsberg, MD PhD, Aeras

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 octubre de 2009

Finalización primaria (Actual)

1 de diciembre de 2010

Finalización del estudio (Actual)

1 de diciembre de 2013

Fechas de registro del estudio

Enviado por primera vez

24 de febrero de 2015

Primero enviado que cumplió con los criterios de control de calidad

26 de febrero de 2015

Publicado por primera vez (Estimar)

2 de marzo de 2015

Actualizaciones de registros de estudio

Última actualización publicada (Estimar)

3 de marzo de 2015

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

27 de febrero de 2015

Última verificación

1 de febrero de 2015

Más información

Términos relacionados con este estudio

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