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

17 juli 2018 bijgewerkt door: 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.

Studie Overzicht

Toestand

Voltooid

Conditie

Gedetailleerde beschrijving

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).

Studietype

Ingrijpend

Inschrijving (Werkelijk)

72

Fase

  • Niet toepasbaar

Contacten en locaties

In dit gedeelte vindt u de contactgegevens van degenen die het onderzoek uitvoeren en informatie over waar dit onderzoek wordt uitgevoerd.

Studie Locaties

    • Gelderland
      • Ede, Gelderland, Nederland, 6718ZB
        • NIZO

Deelname Criteria

Onderzoekers zoeken naar mensen die aan een bepaalde beschrijving voldoen, de zogenaamde geschiktheidscriteria. Enkele voorbeelden van deze criteria zijn iemands algemene gezondheidstoestand of eerdere behandelingen.

Geschiktheidscriteria

Leeftijden die in aanmerking komen voor studie

18 jaar tot 55 jaar (Volwassen)

Accepteert gezonde vrijwilligers

Ja

Geslachten die in aanmerking komen voor studie

Mannelijk

Beschrijving

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.

Studie plan

Dit gedeelte bevat details van het studieplan, inclusief hoe de studie is opgezet en wat de studie meet.

Hoe is de studie opgezet?

Ontwerpdetails

  • Primair doel: Behandeling
  • Toewijzing: Gerandomiseerd
  • Interventioneel model: Parallelle opdracht
  • Masker: Verdrievoudigen

Wapens en interventies

Deelnemersgroep / Arm
Interventie / Behandeling
Placebo-vergelijker: 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).
Experimenteel: 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.

Wat meet het onderzoek?

Primaire uitkomstmaten

Uitkomstmaat
Maatregel Beschrijving
Tijdsspanne
Stool consistency
Tijdsspanne: 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
Tijdsspanne: 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)

Secundaire uitkomstmaten

Uitkomstmaat
Maatregel Beschrijving
Tijdsspanne
Stool frequency
Tijdsspanne: 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
Tijdsspanne: 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
Tijdsspanne: 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)

Medewerkers en onderzoekers

Hier vindt u mensen en organisaties die betrokken zijn bij dit onderzoek.

Medewerkers

Onderzoekers

  • Studie directeur: Van Schaik, NIZO food research

Studie record data

Deze datums volgen de voortgang van het onderzoeksdossier en de samenvatting van de ingediende resultaten bij ClinicalTrials.gov. Studieverslagen en gerapporteerde resultaten worden beoordeeld door de National Library of Medicine (NLM) om er zeker van te zijn dat ze voldoen aan specifieke kwaliteitscontrolenormen voordat ze op de openbare website worden geplaatst.

Bestudeer belangrijke data

Studie start (Werkelijk)

7 december 2017

Primaire voltooiing (Werkelijk)

23 januari 2018

Studie voltooiing (Werkelijk)

16 maart 2018

Studieregistratiedata

Eerst ingediend

15 september 2017

Eerst ingediend dat voldeed aan de QC-criteria

28 september 2017

Eerst geplaatst (Werkelijk)

4 oktober 2017

Updates van studierecords

Laatste update geplaatst (Werkelijk)

18 juli 2018

Laatste update ingediend die voldeed aan QC-criteria

17 juli 2018

Laatst geverifieerd

1 juli 2018

Meer informatie

Termen gerelateerd aan deze studie

Aanvullende relevante MeSH-voorwaarden

Andere studie-ID-nummers

  • NL62453.028.17

Plan Individuele Deelnemersgegevens (IPD)

Bent u van plan om gegevens van individuele deelnemers (IPD) te delen?

NEE

Informatie over medicijnen en apparaten, studiedocumenten

Bestudeert een door de Amerikaanse FDA gereguleerd geneesmiddel

Nee

Bestudeert een door de Amerikaanse FDA gereguleerd apparaatproduct

Nee

product vervaardigd in en geëxporteerd uit de V.S.

Ja

Deze informatie is zonder wijzigingen rechtstreeks van de website clinicaltrials.gov gehaald. Als u verzoeken heeft om uw onderzoeksgegevens te wijzigen, te verwijderen of bij te werken, neem dan contact op met register@clinicaltrials.gov. Zodra er een wijziging wordt doorgevoerd op clinicaltrials.gov, wordt deze ook automatisch bijgewerkt op onze website .

Klinische onderzoeken op E. coli strain E1392-75-2A

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