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Completed

NCT Number: NCT04491266

Tolerability and Modulatory Action of the Butyrate Releaser N-(1-carbamoyl-2-phenyl-ethyl) Butyramide

Accumulating evidence is showing that gut microbiota could play a key role in gastrointestinal tract and immune system development and function. Many beneficial effects elicited by gut microbiota are mediated its metabolites. Short chain fatty acids (SCFAs) are major metabolites produced by gut microbiota. Among SCFA, butyrate has emerged as pivotal regulator of many gastrointestinal function and immune system development and function.

Butyrate is produced by intestinal microbial fermentation of resistant starches and dietary fiber. It regulates several beneficial intestinal and extra-intestinal functions, among the first it serves as the primary energy source for the gut epithelium, increases mineral absorption, stimulates proliferation and differentiation of normal colon epithelial cells, improves the gut barrier function by stimulation of the formation of mucin, antimicrobial peptides, and tight-junction proteins, interacts with the immune system and has anti-inflammatory effects.

Butyrate also seems to regulate the expression of antimicrobial peptides in particular upregulating transcription of cathelicidin thanks to his action of histone deacetylase inhibitor and it has been shown to induce human β-defensin 2 (HBD-2) mRNA expression in colonocytes, although there are few publications reporting its regulation of defensins (Berni Canani R et al. W J Gastroenterol. 2011;17(12):1519). Preliminary data showed that breast milk contains butyrate. Butyrate could be an ideal compound for infant formulas for an efficient regulation of a number of protective actions at gastrointestinal tract level and at systemic level.

A new butyrate releaser, useful for all the known applications of butyrate, presenting physiochemical characteristics suitable for easy oral administration (free from unpleasant organoleptic properties of butyrate): N-(1-carbamoyl-2-phenyl-ethyl) butyramide (FBA) has been developed. The molecule is a butyrate amide with the amino acid phenylalanine, solid, odourless, tasteless, stable at gastric pH, and able to release butyrate constantly throughout gastrointestinal tract.

The aim of the study was to evaluate tolerability and safety profile of a nutritional intervention with FBA in formula fed at term neonates. The effects on the expression of innate immunity biomarkers as well as on neonatal gut function were also assessed.

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Key information

Conditions

Age range

Up to 3 day

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

University of Naples Federico II

Naples, 80131, Italy

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • otherwise healthy formula fed-neonates
  • born at term (>37 gestational age)
  • adequate weight for gestational age

Exclusion criteria

  • twins,
  • infants with history of severe asphyxia,
  • meconium aspiration syndrome,
  • immunodeficiency,
  • congenital infections,
  • genetic diseases and chromosomal abnormalities,
  • malformations,
  • insufficient reliability or presence of conditions that made the patient's compliance with the protocol unlikely,
  • infants with any other condition which, in the opinion of the Investigator, is likely to interfere with the ability of the infant to ingest food, or the normal growth and development of the infant, or the evaluation of the infant.

In addition, as maternal exclusion factors:

  • history of immune diseases,
  • tumors,
  • infectious or inflammatory diseases that required antibiotic therapy during pregnancy,
  • diabetes,
  • gestosis,
  • dyslipidemia,
  • positive vaginal swab for Group B Streptococcus,
  • prolonged rupture of membranes.

Treatment and study plan

FBA

Dietary Supplement

N-(1-carbamoyl-2-phenyl-ethyl) butyramide (FBA) has been developed.

Placebo

Dietary Supplement

maltodextrins

Primary outcomes

  1. safety and tolerability: adverse events

    Time frame: up to 28 days

    number and proportion of subjects with adverse events

Secondary outcomes

  1. percentage of subjects with infantile colics

    Time frame: up to 28 days

    rate of subjects with infantile colics

  2. daily number of bowel movements

    Time frame: up to 28 days

    daily number of bowel movements

  3. stool consistency

    Time frame: up to 28 days

    stool consistency

  4. daily number of regurgitation episodes

    Time frame: up to 28 days

    daily number of regurgitation episodes

  5. fecal levels of of β-defensins 2 (HβD-2)

    Time frame: up to 28 days

  6. change of secretory immunoglobulin A (sIgA)

    Time frame: up to 28 days

Sponsors and collaborators

Lead sponsor

Federico II University

Other

Registry information

Official study title

Tolerability and Modulatory Action on Neonatal Gastrointestinal Function and Immunity of the Butyrate Releaser N-(1-carbamoyl-2-phenyl-ethyl) Butyramide as New Component for Infant Formula

Important dates

Study start
2012
Primary completion
2013
Study completion
2013
First posted
Jul 29, 2020
Registry last updated
Aug 12, 2020

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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