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New formula aims to help Milk-Allergic babies keep food down

NCT ID NCT07592182

Disease control Sponsor: Lactalis Source: ClinicalTrials.gov ↗

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Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting This study
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
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Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

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Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
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Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

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Status unknown
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First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 2 times

Summary

This study tests whether a special anti-regurgitation formula, made from extensively hydrolysed casein, is safe and well-tolerated in infants with cow's milk protein allergy (CMPA). About 55 babies aged 1 to 9 months will take part. The formula is given in a controlled food challenge, and then over a longer period to check growth and allergy symptoms. The goal is to provide a better feeding option for infants who both have CMPA and spit up frequently.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
extensively hydrolysed anti-regurgitation casein-based formula
What this could lead to
If successful, this formula could offer a safe, ready-to-use option for infants with cow's milk protein allergy who also have reflux, reducing the need for more expensive or restrictive alternatives.
What could go wrong
This is a small, early-stage study (55 infants) that has not yet started recruiting. The formula may still trigger allergic reactions in some babies, and results may not apply to all infants with CMPA.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Phase

Not a phased trial

Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.

Participants

About 55 people

The number the study aims to enrol. It can still change while the study runs.

Expected to start

May 2026

An estimate. Start dates often move.

Expected to finish

Jul 2028

An estimate. End dates often move.

Lead sponsor

A company

The lead sponsor is a pharmaceutical, biotech, or medical-device company.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Ages

1 month to 9 months

Sex

Anyone

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: I1. Age ≥ 1 month and \< 9 months, I2. Exclusively formula fed and planning to be formula-fed for the duration of the study (food diversification allowed), I3. With: 1. a suspicion of CMPA based on suggestive allergic symptoms * CoMISS score \> 10 * And/or acute allergic symptoms * And/or symptoms suggestive of a Food Protein-Induced Enterocolitis Syndrome (FPIES) (major criteria and \<3 minor criteria as per consensus guidelines) (Nowak-Węgrzyn et al. 2017; Beaudoin et al. 2025); OR 2. a confirmed diagnosis of CMPA within the two months before inclusion: * IgE-mediated CMPA (documented history of allergic reaction grade ≤ 3 according to the ordinal food allergy severity score oFASS-5 (Fernández-Rivas et al. 2022) following milk protein ingestion, and sensitization to CMP: blood IgE level specific to cow milk≥ 5 kU/L, or positive skin prick test with papule with fresh cow's milk ≥ 8 mm * or non-IgE-mediated CMPA (documented history of eviction/reintroduction test concluding to CMPA), * or FPIES (major criteria and ≥3 minor criteria as per consensus guidelines (Nowak-Węgrzyn et al. 2017; Beaudoin et al. 2025), I4. With a written informed consent signed by the father and mother or legal representative(s), I5. With parents willing to complete questionnaires, records, and diaries associated to the study and to complete all clinical visits, I6. With parents willing to achieve all study interventions, I7. At least one of the legal representatives is affiliated with a social security scheme. Exclusion Criteria: E1. Birthweight \< 2500 g, E2. Gestational age \< 37 weeks, E3. Breastfeeding at the time of inclusion and throughout the study period, E4. Already fed with an AAF, or with the investigational formula EHF-AR, E5. History of anaphylactic reaction grade 4 or 5 according to classification oFASS-5 (Fernández-Rivas et al. 2022), or of severe FPIES (previous reaction with any change in behaviour from baseline, any pallor and dehydration requiring intravenous fluids), after mammalian milk exposure, E6. Diagnosed or reported fever and/or infectious diseases, or current systemic infections, or history of congenital infections, E7. History / diagnosis of: 1. GI disease or abnormalities (i.e. short bowel syndrome, chronic intestinal diseases, or GI malformations), 2. Or Other malformations, congenital cardiovascular, kidney, liver, pancreas, metabolic or neurological diseases, 3. Or Immunodeficiency, or chronic infection requiring long-term treatment, 4. Or Genetic diseases and chromosomal abnormalities, E8. Suspected or confirmed food allergies or intolerances, other than CMPA, E9. Currently enrolled in another clinical study, or in exclusion period from a previous clinical study, E10. Whose legal representatives have psychological or linguistic incapability to sign the informed consent, E11. Impossibility to contact the legal representatives in case of emergency. After V1, the participant will be excluded from participation in this trial if he/she fulfils the following criteria: E12. No allergic symptoms following the OFC with a standard CMPF.

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Conditions

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As listed by the trial registrant

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