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PTM202 and Modulation of Host Resistance to Diarrheagenic E. Coli (APA12/PANTER)

17 de julio de 2018 actualizado por: NIZO Food Research

PTM202 and Modulation of Host Resistance to Diarrheagenic Escherichia Coli in a Randomized, Double-blind, Placebo Controlled Study in Healthy Human Subjects

The APA12/PANTER study is a parallel 3-weeks intervention study. Subjects will be randomly assigned to one of two treatment groups; placebo or PTM202 (n=36 per group). After an overnight fast, subjects will be orally infected with a live, but attenuated, diarrheagenic E. coli at study day 14. At various time points before and after diarrheagenic E. coli challenge an online diary will be kept to record information on stool consistency, frequency and severity of symptoms and stool samples will be collected to determine total fecal wet weight and percentage of fecal wet weight.

Descripción general del estudio

Estado

Terminado

Condiciones

Descripción detallada

The APA12/PANTER study is a randomized, double-blind, placebo-controlled, parallel intervention study of 3 weeks in 72 healthy adults. The study will include 2 arms; PTM202 and placebo. Subjects will be instructed to maintain their usual pattern of physical activity and their habitual food intake, but to standardize their dietary calcium intake. After an overnight fast, subjects will be orally infected with a live, but attenuated, diarrheagenic E. coli (strain E1392-75-2A; collection NIZO food research; dose 1E10 CFU (at study day 14).

At study day 14, 15 and 16 subjects will receive either placebo or PTM202, a dietary formula containing dried bovine colostrum and dried whole egg.

Before and after the diarrheagenic E. coli challenge an online diary will be kept to record information on stool consistency, frequency, severity of symptoms and mediation intake. At various time points before and after diarrheagenic E. coli challenge stool samples will be collected. The main study parameters are Stool consistency (Bristol Stool Scale reported by the subjects in the online diary, and Percentage of fecal wet weight (% determined by freeze-drying).

Secondary study parameters are: Stool frequency (Stools per day reported by the subjects in the online diary), Total fecal wet weight (fecal weight in g/day), and the incidence and severity of Gastro-intestinal symptoms (Gastro-intestinal Symptom Rating Scale reported by the subjects in the online diary).

Tipo de estudio

Intervencionista

Inscripción (Actual)

72

Fase

  • No aplica

Contactos y Ubicaciones

Esta sección proporciona los datos de contacto de quienes realizan el estudio e información sobre dónde se lleva a cabo este estudio.

Ubicaciones de estudio

    • Gelderland
      • Ede, Gelderland, Países Bajos, 6718ZB
        • NIZO

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 55 años (Adulto)

Acepta Voluntarios Saludables

Géneros elegibles para el estudio

Masculino

Descripción

Inclusion Criteria:

  1. Male;
  2. Age between 18 and 55 years;
  3. BMI ≥18 and ≤27 kg/m2;
  4. Healthy as assessed by the NIZO food research medical questionnaire.
  5. Ability to follow verbal and written instructions;
  6. Availability of internet connection;
  7. Signed informed consent;
  8. Willing to accept disclosure of the financial benefit of participation in the study to the authorities concerned;
  9. Willing to accept use of all encoded data, including publication, and the confidential use and storage of all data for at least 15 years;
  10. Willing to comply with study procedures, including collection of stool samples;
  11. Willingness to abstain from high calcium containing products;
  12. Willingness to abstain from alcoholic beverages three days before, during and for four days after diarrheagenic E. coli challenge;
  13. Willingness to abstain from antibiotics, norit, laxatives, nonsteroidal anti-inflammatory drugs (OTC), opiates, antacids, proton pump inhibitors, and antimotility agents (e.g., loperamide) on the three days before, during and for four days after diarrheagenic E. coli challenge.
  14. Willingness to abstain from probiotics three days before, during and for four days after diarrheagenic E. coli challenge;
  15. Willingness to give up blood donation starting 1 month prior to study start and during the entire study;

Exclusion Criteria:

  1. Any confirmed or suspected immunosuppressive or immunodeficient condition including human immunodeficiency virus infection (HIV);
  2. Disease of the GI tract, liver, bile bladder, kidney, thyroid gland (self-reported);
  3. Diarrheagenic E. coli strain (as used in the study) detected in fecal sample at screening;
  4. Evidence of current excessive alcohol consumption or non-therapeutic drug (ab)use);
  5. High titer serum antibodies against CFA-II diarrheagenic E. coli strain (as used in the study) at screening;
  6. History of microbiologically confirmed ETEC or cholera infection in last 3 years;
  7. Known allergy to the following antibiotics: ciprofloxacin, trimethoprim-sulfamethoxazole, and penicillins;
  8. Known allergy to soy, milk- and/or egg;
  9. Mental status that is incompatible with the proper conduct of the study;
  10. Occupation involving handling of ETEC or Vibrio cholerae currently, or in the past 3 years;
  11. Reported average stool frequency of <1 or >3 per day;
  12. Symptoms consistent with Travelers' Diarrhea concurrent with travel to countries where ETEC infection is endemic (most of the developing world) within 3 years prior to dosing, OR planned travel to endemic countries during the length of the study;
  13. Use of antibiotics, norit, laxatives (up till 6 months prior to inclusion), cholesterol lowering agents, antacids, proton pump inhibitors and immune suppressive agents (up till 3 months prior to inclusion);
  14. Vaccination for or ingestion of ETEC, cholera, or E coli heat labile toxin within 3 years prior to inclusion;
  15. Vegans.

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: Triple

Armas e Intervenciones

Grupo de participantes/brazo
Intervención / Tratamiento
Comparador de placebos: Placebo

The placebo will consist of low-lactose isonitrogenous soy product, and will be matched in appearance and flavour to PTM202.

After an overnight fast, subjects will be orally infected with a live, but attenuated, diarrheagenic E. coli (strain E1392-75-2A; collection NIZO food research; dose 1E10 CFU (at study day 14).

After an overnight fast, subjects will be orally infected with a live, but attenuated, diarrheagenic E. coli (strain E1392-75-2A; collection NIZO food research; dose 1E10 CFU (at study day 14).
Experimental: PTM202

PTM202 is a dry powder for reconstitution, comprised of a proprietary mixture of dried bovine colostrum and dried whole egg.

After an overnight fast, subjects will be orally infected with a live, but attenuated, diarrheagenic E. coli (strain E1392-75-2A; collection NIZO food research; dose 1E10 CFU (at study day 14).

After an overnight fast, subjects will be orally infected with a live, but attenuated, diarrheagenic E. coli (strain E1392-75-2A; collection NIZO food research; dose 1E10 CFU (at study day 14).
PTM202 is a dietary formula containing a proprietary mixture of dried bovine colostrum and dried whole egg.

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Stool consistency
Periodo de tiempo: Before challenge (Day 11-13), After challenge (Day 14-18)
Change in stool consistency score (questionnaire) before and after E. coli challenge
Before challenge (Day 11-13), After challenge (Day 14-18)
Relative fecal wet weight
Periodo de tiempo: Before challenge (Day 11-13), After challenge (Day 14-18)
Change in relative fecal wet weight (freeze-drying) before and after E. coli challenge
Before challenge (Day 11-13), After challenge (Day 14-18)

Medidas de resultado secundarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Stool frequency
Periodo de tiempo: Before challenge (Day 11-13), After challenge (Day 14-18)
Change in stool frequency (questionnaire) before and after E. coli challenge
Before challenge (Day 11-13), After challenge (Day 14-18)
Total fecal wet weight
Periodo de tiempo: Before challenge (Day 11-13), After challenge (Day 14-18)
Change in total fecal wet weight (wet weight measurement) before and after E. coli challenge
Before challenge (Day 11-13), After challenge (Day 14-18)
Gastro-intestinal symptoms
Periodo de tiempo: Before challenge (Day 11-13), After challenge (Day 14-18)
Change in gastro-intestinal symptoms (questionnaire) before and after E. coli challenge
Before challenge (Day 11-13), After challenge (Day 14-18)

Colaboradores e Investigadores

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

Patrocinador

Colaboradores

Investigadores

  • Director de estudio: Van Schaik, NIZO food research

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)

7 de diciembre de 2017

Finalización primaria (Actual)

23 de enero de 2018

Finalización del estudio (Actual)

16 de marzo de 2018

Fechas de registro del estudio

Enviado por primera vez

15 de septiembre de 2017

Primero enviado que cumplió con los criterios de control de calidad

28 de septiembre de 2017

Publicado por primera vez (Actual)

4 de octubre de 2017

Actualizaciones de registros de estudio

Última actualización publicada (Actual)

18 de julio de 2018

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

17 de julio de 2018

Última verificación

1 de julio de 2018

Más información

Términos relacionados con este estudio

Términos MeSH relevantes adicionales

Otros números de identificación del estudio

  • NL62453.028.17

Plan de datos de participantes individuales (IPD)

¿Planea compartir datos de participantes individuales (IPD)?

NO

Información sobre medicamentos y dispositivos, documentos del estudio

Estudia un producto farmacéutico regulado por la FDA de EE. UU.

No

Estudia un producto de dispositivo regulado por la FDA de EE. UU.

No

producto fabricado y exportado desde los EE. UU.

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 E. coli strain E1392-75-2A

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