Human Milk Oligosaccharides (HMOs) Post-market Study on Infants (NEHMO) (NeHMO DACH)

Nestlé

Status: Completed

Conditions: Adverse Event; Formula Satisfaction; Tolerance; Growth; Disorder of Intestine

Treatments: Other: HMO-supplemented infant formula

Study type: Interventional

Funder types: Other; Industry

Identifiers

NCT05150288

1806INF- DACH

Details and patient eligibility

About

Human milk oligosaccharides (HMOs) represent the third largest solid component of breast milk. Technology advancements made it possible to supplement infant formulas with HMOs (2'FL, LNnT). Two published RCTs have demonstrated that infant formulas supplemented with 2'FL or 2'FL+LNnT are safe, well-tolerated, support normal grow, and may support healthy GI function and confer immune benefits. The performance of HMOs-supplemented formulas assessed in a real-world setting is complementary to previously conducted RCTs conducted in highly controlled clinical settings. Main objectives will be to monitor the safety & tolerance of HMOs-supplemented formulas in larger and diverse infant populations; to assess the performance of HMOs-supplemented formulas in mixed-fed infants, a population that was not studied in previous RCTs but likely represents a relatively common feeding regimen. Finally, considering the potential health/immune benefits of HMOs, it is also important explore the incidences of illnesses (i.e., respiratory illnesses, GI illnesses, and fever) associated with consuming HMOs-supplemented formulas and compare with breastfed infants data.

Full description

Objectives:

The main objective of this study is to document the growth and feeding tolerance of healthy term infants consuming an infant formula supplemented with HMOs for 8 weeks (56 days), in a real-world setting.

Main endpoints:

1. Growth documented via monitoring the anthropometric parameters including weight, length, head circumference, BMI and their corresponding z-scores (i.e., z-scores for weight-for-age, length-for-age, weight-for-length, head circumference-for-age, and BMI-for-age) calculated using the 2006 WHO Growth Standards
2. Feeding tolerance assessed via monitoring parent-reported overall GI symptom burden measured by the Infant Gastrointestinal Symptom Questionnaire (IGSQ) index score (13-item summary score)

Additional objectives:

To describe the following outcomes in infants fed an infant formula supplemented with HMOs:

1. Formula acceptability
2. Despite there are no expected safety concerns, standard Adverse Events (AEs) monitoring will be implemented during the study

Additional endpoints:

1. Formula acceptability assessed by the Study Formula Satisfaction Questionnaire

2. Reported AEs and Serious Adverse Events (SAEs) including type, incidence, severity, seriousness and relation to study formula consumption as well as concomitant medications and non-pharmacological treatments.

   • Select morbidities of interest (i.e., respiratory illnesses, GI illnesses, and fever) will be collected as part of AE reporting and specific corresponding AE guidance forms will be used to standardize reporting of such AEs

Trial design:

Uncontrolled, single arm, open-label, prospective study in infants (enrolled at postnatal age 7 days to 2 months) fed the study formula for 8 weeks (56 days)

A group of exclusively breastfed infants (BF) will serve as a reference group in parallel to the study arm. For the BF group, Infants must have been exclusively consuming breast milk since birth, and their parent(s) must have made the decision to continue exclusively breastfeeding until at least 4 month of age

Trial population:

Healthy, male and female, term infants, 7 days postnatal age to 2 months of age at the enrollment

Treatment duration:

Total study participation/intervention up to approximately 8 weeks

Enrollment: 106 patients

Sex: All

Ages: 7 days to 2 months old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• Evidence of personally signed and dated informed consent document indicating that the infant's parent(s) have been informed of all pertinent aspects of the study
• Parent(s) are willing and able to fulfill the requirements of the study protocol
• Healthy full term (37-42 weeks gestation) infant
• Be between post-natal age (Date of Birth = Day 0) 7 days to 2 months
• Parent(s) must have independently elected, before enrollment, to formula feed

Exclusion criteria

• Any known intolerance/allergy to cow's milk (formula-fed group only)
• systemic disorders (cardiac, respiratory, endocrinological, hematologic, gastointestinal, or other)
• conditions requireing infant feedings other than those specified in the protocol
• Infants must have been exclusively consuming breast milk since birth, and their parent(s) must have made the decision to continue exclusively breastfeeding until at least 4 month of age

Trial design

Primary purpose: Other

Allocation: Non-Randomized

Interventional model: Parallel Assignment

Masking: None (Open label)

---

106 participants in 3 patient groups

Formula-fed infants

Experimental group

Description:

Infants fed exclusively with experimental formula

Treatment:

Other: HMO-supplemented infant formula

Mixed-fed infants

Experimental group

Description:

Infants receiving breastmilk and experimental formula

Treatment:

Other: HMO-supplemented infant formula

Breast-fed infants

No Intervention group

Description:

Reference group of exclusively breastfed