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

17. juli 2018 oppdatert av: 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.

Studieoversikt

Status

Fullført

Detaljert beskrivelse

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

Intervensjonell

Registrering (Faktiske)

72

Fase

  • Ikke aktuelt

Kontakter og plasseringer

Denne delen inneholder kontaktinformasjon for de som utfører studien, og informasjon om hvor denne studien blir utført.

Studiesteder

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

Deltakelseskriterier

Forskere ser etter personer som passer til en bestemt beskrivelse, kalt kvalifikasjonskriterier. Noen eksempler på disse kriteriene er en persons generelle helsetilstand eller tidligere behandlinger.

Kvalifikasjonskriterier

Alder som er kvalifisert for studier

18 år til 55 år (Voksen)

Tar imot friske frivillige

Ja

Kjønn som er kvalifisert for studier

Mann

Beskrivelse

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.

Studieplan

Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.

Hvordan er studiet utformet?

Designdetaljer

  • Primært formål: Behandling
  • Tildeling: Randomisert
  • Intervensjonsmodell: Parallell tildeling
  • Masking: Trippel

Våpen og intervensjoner

Deltakergruppe / Arm
Intervensjon / Behandling
Placebo komparator: 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).
Eksperimentell: 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.

Hva måler studien?

Primære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Stool consistency
Tidsramme: 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
Tidsramme: 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)

Sekundære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Stool frequency
Tidsramme: 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
Tidsramme: 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
Tidsramme: 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)

Samarbeidspartnere og etterforskere

Det er her du vil finne personer og organisasjoner som er involvert i denne studien.

Samarbeidspartnere

Etterforskere

  • Studieleder: Van Schaik, NIZO food research

Studierekorddatoer

Disse datoene sporer fremdriften for innsending av studieposter og sammendragsresultater til ClinicalTrials.gov. Studieposter og rapporterte resultater gjennomgås av National Library of Medicine (NLM) for å sikre at de oppfyller spesifikke kvalitetskontrollstandarder før de legges ut på det offentlige nettstedet.

Studer hoveddatoer

Studiestart (Faktiske)

7. desember 2017

Primær fullføring (Faktiske)

23. januar 2018

Studiet fullført (Faktiske)

16. mars 2018

Datoer for studieregistrering

Først innsendt

15. september 2017

Først innsendt som oppfylte QC-kriteriene

28. september 2017

Først lagt ut (Faktiske)

4. oktober 2017

Oppdateringer av studieposter

Sist oppdatering lagt ut (Faktiske)

18. juli 2018

Siste oppdatering sendt inn som oppfylte QC-kriteriene

17. juli 2018

Sist bekreftet

1. juli 2018

Mer informasjon

Begreper knyttet til denne studien

Ytterligere relevante MeSH-vilkår

Andre studie-ID-numre

  • NL62453.028.17

Plan for individuelle deltakerdata (IPD)

Planlegger du å dele individuelle deltakerdata (IPD)?

NEI

Legemiddel- og utstyrsinformasjon, studiedokumenter

Studerer et amerikansk FDA-regulert medikamentprodukt

Nei

Studerer et amerikansk FDA-regulert enhetsprodukt

Nei

produkt produsert i og eksportert fra USA

Ja

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