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NCT03307122

Gastrointestinal Tolerance Evaluation of an Infant Formula

Completed NA Last updated 23 May 2018
What this trial tests

NA trial testing Routine Infant Formula 1 in Healthy, Full-term Infants Who Are Formula-fed in 79 participants. Completed in 19 January 2018.

Timeline
21 September 2017
Primary endpoint
19 January 2018
19 January 2018

Quick facts

Lead sponsorSociété des Produits Nestlé (SPN)
PhaseNA
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingquadruple
Primary purposetreatment
Enrollment79
Start date21 September 2017
Primary completion19 January 2018
Estimated completion19 January 2018
Sites8 locations across United States

Drugs / interventions tested

Conditions studied

Sponsor

Société des Produits Nestlé (SPN) — full company profile →

Who can join

Adults 9 Days to 19 Days, any sex, with Healthy, Full-term Infants Who Are Formula-fed. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Prospective, double-blind, randomized study of 2 infant formulas.

Publications & conference data

2 peer-reviewed publications reference this trial (live from Europe PMC):

  1. 2'-Fucosyllactose Is Well Tolerated in a 100% Whey, Partially Hydrolyzed Infant Formula With <i>Bifidobacterium lactis</i>: A Randomized Controlled Trial.
    Storm HM, Shepard J, Czerkies LM, Kineman B, et al · · 2019 · cited 28× · PMID 30906817 · DOI 10.1177/2333794x19833995
  2. Human Milk Oligosaccharides: Decoding Their Structural Variability, Health Benefits, and the Evolution of Infant Nutrition.
    Duman H, Bechelany M, Karav S. · · 2024 · cited 18× · PMID 39796552 · DOI 10.3390/nu17010118

Verify or expand the search:

Other Société des Produits Nestlé (SPN) trials

Trials by the same sponsor.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT03307122.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing