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- Ensayo clínico NCT03301103
PTM202 and Modulation of Host Resistance to Diarrheagenic E. Coli (APA12/PANTER)
PTM202 and Modulation of Host Resistance to Diarrheagenic Escherichia Coli in a Randomized, Double-blind, Placebo Controlled Study in Healthy Human Subjects
Descripción general del estudio
Estado
Condiciones
Intervención / Tratamiento
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
Inscripción (Actual)
Fase
- No aplica
Contactos y Ubicaciones
Ubicaciones de estudio
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Gelderland
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Ede, Gelderland, Países Bajos, 6718ZB
- NIZO
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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;
- Age between 18 and 55 years;
- BMI ≥18 and ≤27 kg/m2;
- Healthy as assessed by the NIZO food research medical questionnaire.
- Ability to follow verbal and written instructions;
- Availability of internet connection;
- Signed informed consent;
- Willing to accept disclosure of the financial benefit of participation in the study to the authorities concerned;
- Willing to accept use of all encoded data, including publication, and the confidential use and storage of all data for at least 15 years;
- Willing to comply with study procedures, including collection of stool samples;
- Willingness to abstain from high calcium containing products;
- Willingness to abstain from alcoholic beverages three days before, during and for four days after diarrheagenic E. coli challenge;
- 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.
- Willingness to abstain from probiotics three days before, during and for four days after diarrheagenic E. coli challenge;
- Willingness to give up blood donation starting 1 month prior to study start and during the entire study;
Exclusion Criteria:
- Any confirmed or suspected immunosuppressive or immunodeficient condition including human immunodeficiency virus infection (HIV);
- Disease of the GI tract, liver, bile bladder, kidney, thyroid gland (self-reported);
- Diarrheagenic E. coli strain (as used in the study) detected in fecal sample at screening;
- Evidence of current excessive alcohol consumption or non-therapeutic drug (ab)use);
- High titer serum antibodies against CFA-II diarrheagenic E. coli strain (as used in the study) at screening;
- History of microbiologically confirmed ETEC or cholera infection in last 3 years;
- Known allergy to the following antibiotics: ciprofloxacin, trimethoprim-sulfamethoxazole, and penicillins;
- Known allergy to soy, milk- and/or egg;
- Mental status that is incompatible with the proper conduct of the study;
- Occupation involving handling of ETEC or Vibrio cholerae currently, or in the past 3 years;
- Reported average stool frequency of <1 or >3 per day;
- 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;
- 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);
- Vaccination for or ingestion of ETEC, cholera, or E coli heat labile toxin within 3 years prior to inclusion;
- Vegans.
Plan de estudios
¿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 |
|---|---|
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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).
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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.
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¿Qué mide el estudio?
Medidas de resultado primarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
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Stool consistency
Periodo de tiempo: Before challenge (Day 11-13), After challenge (Day 14-18)
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Change in stool consistency score (questionnaire) before and after E. coli challenge
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Before challenge (Day 11-13), After challenge (Day 14-18)
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Relative fecal wet weight
Periodo de tiempo: Before challenge (Day 11-13), After challenge (Day 14-18)
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Change in relative fecal wet weight (freeze-drying) before and after E. coli challenge
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Before challenge (Day 11-13), After challenge (Day 14-18)
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Medidas de resultado secundarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
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Stool frequency
Periodo de tiempo: Before challenge (Day 11-13), After challenge (Day 14-18)
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Change in stool frequency (questionnaire) before and after E. coli challenge
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Before challenge (Day 11-13), After challenge (Day 14-18)
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Total fecal wet weight
Periodo de tiempo: Before challenge (Day 11-13), After challenge (Day 14-18)
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Change in total fecal wet weight (wet weight measurement) before and after E. coli challenge
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Before challenge (Day 11-13), After challenge (Day 14-18)
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Gastro-intestinal symptoms
Periodo de tiempo: Before challenge (Day 11-13), After challenge (Day 14-18)
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Change in gastro-intestinal symptoms (questionnaire) before and after E. coli challenge
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Before challenge (Day 11-13), After challenge (Day 14-18)
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Colaboradores e Investigadores
Patrocinador
Colaboradores
Investigadores
- Director de estudio: Van Schaik, NIZO food research
Fechas de registro del estudio
Fechas importantes del estudio
Inicio del estudio (Actual)
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 (Actual)
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
Otros números de identificación del estudio
- NL62453.028.17
Plan de datos de participantes individuales (IPD)
¿Planea compartir datos de participantes individuales (IPD)?
Información sobre medicamentos y dispositivos, documentos del estudio
Estudia un producto farmacéutico regulado por la FDA de EE. UU.
Estudia un producto de dispositivo regulado por la FDA de EE. UU.
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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NIZO Food ResearchFrieslandCampinaTerminado
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NIZO Food ResearchTerminadoGastroenteritis | Diarrea | Infecciones bacterianas | Infecciones por Escherichia ColiPaíses Bajos
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HealthCore-NERINational Heart, Lung, and Blood Institute (NHLBI)TerminadoHepatitis C | TalasemiaEstados Unidos, Reino Unido, Canadá
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PATHRetiradoDisentería por Shigella SonneiEstados Unidos