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Clinical Trial Summary

This randomized, double-blind, controlled intervention trial aims to evaluate the safety and efficacy of a starter infant formula supplemented with an HMO blend and a probiotic, and will provide evidence on the safety and efficacy of the innovative prebiotic/ probiotic blend to support age-appropriate infant growth, a healthy gut microbiome, gastrointestinal (GI) tolerance and GI health, and immune development.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT06073652
Study type Interventional
Source Société des Produits Nestlé (SPN)
Contact
Status Active, not recruiting
Phase N/A
Start date July 5, 2023
Completion date November 2024

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