IP Library Granted Patent US 12,357,647
Granted Patent B2
US 12,357,647 · App. 17/244,437 · Granted Jul 15, 2025

Compositions for use in the prevention or treatment of necrotizing enterocolitis in infants and young children

Inventor: Per Torp Sangild (Copenhagen NV, GB)
Assignee: Societe des Produits Nestle S.A.
A61K31/702A23L33/10A23L33/125A23L33/135A23L33/40A61K35/741A61K35/745A61K35/747A23V2002/00A23V2400/151A23V2400/165A23V2400/175A23V2400/245A23V2400/519A23V2400/529A23V2400/531A23V2400/533
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Quick Facts
Patent No.
US 12,357,647
App. No.
17/244,437
Granted
Jul 15, 2025
Kind
B2
Abstract

The invention discloses a composition comprising LNT and at least another human milk oligosaccharide or precursor thereof, for use in preventing and/or treating necrotizing enterocolitis in infants and young children.

Claims (6)

1. A method of treating or decreasing incidence of growth delay associated with enteral feeding tolerance in an infant or young child in need thereof, the method comprising administering a composition to the infant or young child, the composition comprising lacto-N-tetraose (LNT), lacto-N-neotetraose (LNnT), 3′ sialyllactose (3-SL), 6′ sialyllactose (6-SL), and 2′-fucosyllactose (2-FL) as the only human milk oligosaccharides in the composition, wherein the composition comprises the LNT and the LNnT in a ratio LNT:LNnT between 5:1 and 1:2.

2. The method according to claim 1 , wherein each of the lacto-N-tetraose (LNT), the lacto-N-neotetraose (LNnT), the 3′ sialyllactose (3-SL), the 6′ sialyllactose (6-SL), and the 2′-fucosyllactose (2-FL) are present in an amount from 0.1 to 20 g/L of the composition.

3. The method according to claim 1 , wherein the composition further comprises at least one probiotic in an amount of from 10 3 to 10 12 cfu/g of the composition (dry weight).

4. The method according to claim 1 , wherein the composition is in a form selected from the group consisting of an infant formula, a starter infant formula, a follow-on infant formula, a baby food, an infant cereal composition, a growing-up milk, a fortifier and a supplement.

5. The method according to claim 1 , wherein the composition is administered to the infant or young child before and/or during the weaning period.

6. The method according to claim 1 , wherein the infant or young child is selected from the group consisting of preterm infants, small for gestational age infants, and infants born by C-section.

Assignments (3)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 16, 2025
From: GLYCOM A/S
To: NESTEC S.A.
Reel/Frame 071418/0660 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 16, 2025
From: SANGILD, PER TORP; UNIVERSITY OF COPENHAGEN
To: GLYCOM A/S
Reel/Frame 071625/0931 →
MERGER Recorded Jun 16, 2025
From: NESTEC S.A.
To: SOCIETE DES PRODUITS NESTLE S.A.
Reel/Frame 071625/0971 →
Priority Claims (1)
EP 13193056 · Nov 15, 2013 · regional
Continuity (2)
Division 15036854
Related Publication 20220008444A1 · Jan 13, 2022
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