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NCT05369494

Infants Fed a Hydrolyzed Infant Formula

Completed NA Last updated 1 May 2024
What this trial tests

NA trial testing Hydrolyzed protein infant formula with oligosaccharides in Gastrointestinal Tolerance in 33 participants. Completed in 18 November 2023.

Timeline
7 May 2022
Primary endpoint
23 June 2023
18 November 2023

Quick facts

Lead sponsorAbbott Nutrition
PhaseNA
StatusCompleted
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposeother
Enrollment33
Start date7 May 2022
Primary completion23 June 2023
Estimated completion18 November 2023
Sites7 locations across United States

Drugs / interventions tested

Conditions studied

Sponsor

Abbott Nutrition — full company profile →

Who can join

Adults 0 Days to 90 Days, any sex, with Gastrointestinal Tolerance. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The purpose of this non-randomized, multi-center study is to evaluate the growth, tolerance and compliance of an extensively hydrolyzed infant formula in an intended use population of infants.

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

  1. Tolerance of Infants Fed a Hydrolyzed Rice Infant Formula with 2′-Fucosyllactose (2′-FL) Human Milk Oligosaccharide (HMO)
    · 2024

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Other Abbott Nutrition 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/NCT05369494.

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