Trial intelligence / Profile preview

B. infantis Supplementation in Healthy Breastfed Infants

NCT02286999Phase 1Withdrawn

Start
Oct 2015
Primary completion
Jan 2018
Modality
Live Biotherapeutic Products
Countries
1
01

Overview

Phase 1, randomised, double-blind trial in atopic dermatitis (AD) and food allergy comparing B. infantis with Placebo (2 arms). Primary endpoints: Pharmacologically effective dose (ED) of B. infantis at 6 weeks and Safety of Probiotic Supplementation at 2 years. Planned start Oct 2015; status: withdrawn.

02

Drugs

Bifidobacterium longum subsp. infantis
03

Conditions

atopic dermatitis (AD)food allergy

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