Hypoallergenicity of a Hydrolyzed Rice Protein-based Formula in Infants and Young Children With Cow's Milk Protein Allergy

NCT ID: NCT06633289

Last Updated: 2025-07-01

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

RECRUITING

Clinical Phase

NA

Total Enrollment

67 participants

Study Classification

INTERVENTIONAL

Study Start Date

2024-11-05

Study Completion Date

2026-10-31

Brief Summary

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The purpose of the study is to determine whether a new hydrolyzed rice protein-based formula is hypoallergenic in infants and young children with documented Immunoglobulin E (IgE)-mediated Cow Milk Protein Allergy (CMPA).

Detailed Description

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Conditions

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Cow's Milk Protein Allergy

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

CROSSOVER

Primary Study Purpose

OTHER

Blinding Strategy

QUADRUPLE

Participants Caregivers Investigators Outcome Assessors

Study Groups

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Experimental formula-Control formula

Blinded cross-over oral food challenge sequence starting by Experimental formula followed by Control.

Following the crossover phase, children who passed the oral food challenge will consume the open label experimental formula at home during 7 days.

Group Type OTHER

Experimental formula

Intervention Type OTHER

New hydrolyzed rice protein-based formula

Control formula

Intervention Type OTHER

Commercially available amino acid-based formula.

Control formula-Experimental formula

Blinded cross-over oral food challenge sequence starting by Control followed by Experimental formula.

Following the crossover phase, children who passed the oral food challenge will consume the open label experimental formula at home during 7 days.

Group Type OTHER

Experimental formula

Intervention Type OTHER

New hydrolyzed rice protein-based formula

Control formula

Intervention Type OTHER

Commercially available amino acid-based formula.

Interventions

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Experimental formula

New hydrolyzed rice protein-based formula

Intervention Type OTHER

Control formula

Commercially available amino acid-based formula.

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

1. Written informed consent has been obtained from at least one parent (or legally acceptable representative \[LAR\]), if applicable)
2. Child gestational age ≥ 37 completed weeks
3. Child aged ≥ 60 days and less than 36 months at enrollment
4. Documented IgE-mediated CMPA no more than 6 months prior to enrollment
5. Child is receiving a strict cow's milk elimination diet and will continue receiving this diet until the completion of the study
6. Child's parent(s) and LAR (if applicable) is of legal age of majority, must have parental authority, must understand the informed consent form and other study documents, and are willing and able to fulfill the requirements of the study protocol

Exclusion Criteria

1. Child is exclusively breastfed
2. Any chronic medical diseases (except atopic eczema), chromosomal or major congenital anomalies
3. Congenital heart disease or treatment by B-blockers
4. Major gastrointestinal disease / abnormalities (other than CMPA)
5. Known or suspected soy allergy
6. Glucose-galactose malabsorption
7. Immunodeficiency
8. Children who are unable to discontinue antihistamine use (excluding eye drops) within 7 days prior to a food challenge and oral steroid use within 14 days prior to enrollment
9. Persistent wheeze or chronic respiratory disease
10. Severe uncontrolled eczema or urticaria
11. Rice protein allergy or intolerance (e.g., rice protein-induced enterocolitis syndrome), or allergy to any ingredient in the formulas
12. Child's parent has other medical or psychiatric condition that, in the judgement of the Investigator, would make the child inappropriate for entry into the study
13. Currently participating or having participated in another interventional clinical study within 4 weeks prior to enrollment
14. Child's parents have not reached legal age of majority (18 years).
Minimum Eligible Age

60 Days

Maximum Eligible Age

3 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Société des Produits Nestlé (SPN)

INDUSTRY

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Locations

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Charité - Universitätsmedizin Berlin Klinik für Pädiatrie m.S. Pneumologie/Immunologie

Berlin, , Germany

Site Status NOT_YET_RECRUITING

IRCCS Azienda Ospedaliero Universitaria Meyer Viale Gaetano Pieraccini

Florence, , Italy

Site Status NOT_YET_RECRUITING

Ospedale dei Bambini V. Buzzi Via Castelvetro, 32

Milan, , Italy

Site Status NOT_YET_RECRUITING

Universiy of Naples Federico II

Naples, , Italy

Site Status RECRUITING

Azienda Ospedaliero Universitaria di Parma, Italy

Parma, , Italy

Site Status NOT_YET_RECRUITING

Nicolaus Copernicus University in Torun

Bydgoszcz, , Poland

Site Status NOT_YET_RECRUITING

Centrum Medyczne Plejady

Krakow, , Poland

Site Status NOT_YET_RECRUITING

Jagiellonian University Medical College

Krakow, , Poland

Site Status NOT_YET_RECRUITING

Wojewodzki Szpital Specjalistyczny im. M. Kopernika

Lodz, , Poland

Site Status NOT_YET_RECRUITING

BioMedical Centers sp. z o.o.

Warsaw, , Poland

Site Status NOT_YET_RECRUITING

Pediatrics Department at the Medical University of Warsaw

Warsaw, , Poland

Site Status NOT_YET_RECRUITING

Countries

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Germany Italy Poland

Central Contacts

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Julia Mauger

Role: CONTACT

(+41) 79 201 9835

Facility Contacts

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Birgit Kalb, MD

Role: primary

Francesca Mori, MD

Role: primary

Enza D'Auria, Prof.

Role: primary

Roberto Berni Canani, Prof.

Role: primary

Susanna Maria Roberta Esposito

Role: primary

Aneta KROGULSKA, MD PhD, Prof

Role: primary

Marta Żołnowska, MD

Role: primary

Urszula JEDYNAK-WĄSOWICZ, MD

Role: primary

Agnieszka Brzozowska, MD

Role: primary

Karolina Kołakowska, MD

Role: primary

+48728455770

Agnieszka Szczukocka-Zych, MD PhD

Role: primary

Other Identifiers

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2115INF

Identifier Type: -

Identifier Source: org_study_id

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