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Severe Acute MalnutritionMEND-SAMNCT06869850

Milk Fat Globule Membrane-Enhanced RUTF for Children With Severe Acute Malnutrition

A study testing MFGM-RUTF (milk fat globule membrane ready-to-use therapeutic food), S-RUTF (standard ready-to-use therapeutic food) and Amoxicillin in people with Severe Acute Malnutrition and Cognitive Impairment, run by Washington University School of Medicine at 10 sites in Sierra Leone.

Recruiting

Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record

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Trial summary

The goal of this clinical trial is to test the use of milk fat globule membrane (MFGM) in ready-to-use therapeutic food (RUTF) in children with severe acute malnutrition in Sierra Leone. Read more about this study

Who is it for?
Ages 6 to 59 months
What is being tested?
MFGM-RUTF (milk fat globule membrane ready-to-use therapeutic food), S-RUTF (standard ready-to-use therapeutic food) and Amoxicillin
Type of treatment
Pill or oral medicine
Could I receive a placebo?
No, everyone receives an active treatment
How many people
1,600 participants
Where
10 sitesSierra Leone
Study dates
22 Sep 2025to 1 Dec 2027
Phase
Interventional

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 6 to 59 months
  • All sexes
  • No healthy volunteers
  • Child

Who may be able to join

  • 6-59 months of age
  • Reside within the catchment area of a participating clinic
  • mid-upper arm circumference < 11.5 cm and/or weight-for-length z-score < -3 and/or presence of bilateral pedal pitting edema
  • willingness to comply with all study procedures and availability for the duration of the study, including no plan to move from the catchment area of a participating clinic

Who cannot join

  • Features of complicated SAM: inability to tolerate a 30 g test dose of RUTF, breathing difficulties, mental status changes, sepsis, diarrhea with severe dehydration, and/or physician/nursing clinical assessment that the child needs immediate hospitalization
  • Participation in a separate therapeutic feeding program within the past month
  • Known allergy to study food ingredient (peanut, milk, fish)
  • Clinically evident developmental delay (most often determined based on research nursing assessment of physical appearance, movement, and informal discussion with caregiver)
  • Presence of a chronic severe medical condition (other than tuberculosis and HIV), such as congenital heart disease

Trial locations and contacts

10 sites in 1 country. Contact the study team or a site near you to ask about taking part.

Mark J Manary, MD contact

+1 314-454-2341

manarymj@wustl.edu

Kevin B Stephenson, MD contact

+1-314-749-8849

k.stephenson@wustl.edu

10 sites in 1 country

Sierra Leone10 sites, 10 recruiting
  • Bandajuma

    Bandajuma, Pujehun

    Ibrahim A Bangura, +232-77-330360, affieibrahim@gmail.com

    Recruiting
  • Bandasuma

    Bandasuma, Pujehun

    Ibrahim A Bangura, +232-77-330360, affieibrahim@gmail.com

    Recruiting
  • Bendu Malen

    Bendu Malen, Pujehun

    Ibrahim A Bangura, +232-77-330360, affieibrahim@gmail.com

    Recruiting
  • Gbondapi

    Gbondapi, Pujehun

    Ibrahim A Bangura, +232-77-330360, affieibrahim@gmail.com

    Recruiting
  • Jendema

    Jendema, Pujehun

    Ibrahim A Bangura, +232-77-330360, affieibrahim@gmail.com

    Recruiting
  • Potoru

    Potoru, Pujehun

    Ibrahim A Bangura, +232-77-330360, affieibrahim@gmail.com

    Recruiting
  • Static

    Pujehun, Pujehun

    Ibrahim A Bangura, +232-77-330360, affieibrahim@gmail.com

    Recruiting
  • Sahn Malen

    Sahn Malen, Pujehun

    Ibrahim A Bangura, +232-77-330360, affieibrahim@gmail.com

    Recruiting
  • Taninahun

    Taninahun, Pujehun

    Ibrahim A Bangura, +232-77-330360, affieibrahim@gmail.com

    Recruiting
  • Zimmi

    Zimmi, Pujehun

    Ibrahim A Bangura, +232-77-330360, affieibrahim@gmail.com

    Recruiting

Other trials in Sierra Leone

About this study

Official title: MFGM-EnhaNceD RUTF for Children With SAM

The goal of this clinical trial is to test the use of milk fat globule membrane (MFGM) in ready-to-use therapeutic food (RUTF) in children with severe acute malnutrition in Sierra Leone. The main questions it aims to answer are:

  • Will the inclusion of MFGM in RUTF for 6-59-month-old Sierra Leonean children with severe acute malnutrition improve their neurodevelopment?
  • Will the inclusion of MFGM in RUTF for 6-59-month-old Sierra Leonean children with severe acute malnutrition reduce its worst consequences: death, hospitalization, and remaining severely malnourished despite treatment?
Read more

Researchers will compare the MFGM-containing RUTF to standard RUTF, which contains skim milk powder.

Participants will:

  • undergo measurement of length, weight, mid-upper arm circumference, and nutritional edema assessment every two weeks during severe malnutrition treatment
  • be treated with either MFGM-RUTF or standard RUTF at a dose of 2 sachets per day for up to 12 weeks
  • undergo neurodevelopmental testing using the Malawi Developmental Assessment Tool at the end of SAM treatment and 6 months later
  • a subset of participants will undergo blood spot collection and stool sample collection
Read the detailed description

Globally, approximately 15 million children are suffering from severe acute malnutrition (SAM) at any one time, a number that has not declined in recent decades despite significant technological advancements in agriculture and food science. SAM is a condition of total-body depletion of the nutrients required for health and development; without treatment, 50% of affected children will die. Whereas historically children with SAM were admitted to and treated within hospitals, the advent of ready-to-use therapeutic food (RUTF) and community-based management of acute malnutrition revolutionized SAM care by allowing it to occur safely and successfully by the child's caregiver in their own home.

RUTF was designed to provide the nutrients required for physical recovery in a safe, palatable format. It is equal parts peanut paste, sugar, vegetable oil, and skim milk powder, with added micronutrients and emulsifier. At inception, attention was not specifically paid to how RUTF's composition might impact neurodevelopmental recovery in children with SAM. Research over the past decade has revealed that even following successful treatment with RUTF, children diagnosed with SAM still score 1-3 standard deviations below age-based expectations on neurodevelopmental tests. This suggests that the nutrient profile of standard RUTF is not sufficient to recover the developmental damage incurred by SAM.

Recently, progress has been made toward improving the developmental trajectory of children with SAM by altering RUTF. A randomized, blinded trial in Malawi including 2,500 children with SAM showed that improving the polyunsaturated fatty acid (PUFA) profile of RUTF by reducing linoleic acid and adding docosahexaenoic acid (DHA) yields superior neurodevelopment 6 months after treatment, by 0.19 standard deviations on a standardized, culturally adapted neurodevelopmental test. This demonstrates that neurodevelopmental recovery in SAM is sensitive to the lipid profile of RUTF. Despite the benefits of improved PUFA RUTF, however, children with SAM remained 1 standard deviation below expectations in neurodevelopment.

The milk fat globule membrane (MFGM) in mammalian milk contains a host of nutrients and bioactive compounds supportive of physical health and brain development. Bovine MFGM added to infant formula has been tested in several clinical trials and has demonstrated a reduction in infectious episodes, such as diarrhea and ear infections, as well as improvement in cognitive development, compared with infant formula not containing MFGM. In these trials and others, MFGM has been shown to be safe and well-tolerated. Currently, RUTF contains skim milk powder as its high-quality protein source, and peanut and vegetable oils as the primary sources of fat. These vegetable fat sources are deficient in the lipids provided by MFGM: sphingolipids, cholesterol, and other phospholipids such as phosphatidylcholine and phosphatidylethanolamine, all of which play roles in brain development. It is possible that the lipids contained in MFGM may further support neurodevelopmental recovery in SAM children.

By acting as a natural emulsifier, MFGM also offers a food formulation advantage that is relevant to children with SAM. Animal model studies have demonstrated that emulsifiers can compromise the gut barrier. Children with SAM have damaged small intestinal barrier function, which can lead to translocation of gut bacteria and resulting systemic infection. As RUTF will compose nearly 100% of a child's intake for the duration of treatment - up to 3 months - it is possible that inclusion of emulsifier may impede gut healing and recovery. Considering this concern, the Manary lab ran a clinical trial in 2018-2019 testing a novel formulation of RUTF designed with oat in place of some skim milk powder and peanut, and without hydrogenated vegetable oil (standard emulsifier), because oat acts as a natural emulsifier. In this trial, children with SAM receiving the oat-RUTF had 10% absolute higher recovery and a 33% relative reduction in the worst SAM outcomes (death, hospitalization, or remaining severely malnourished). Like oat, MFGM in RUTF allows for omission of emulsifier and may yield similar benefits.

Given (1) the repeated finding that adding MFGM to infant formulas improves neurodevelopment, (2) the impaired neurodevelopment of children with SAM, (3) the current RUTF formulation lacking neuro-supportive fats provided by MFGM, (4) MFGM's natural activity as an emulsifier, and (5), the reality that RUTF provides the sole source of nutrition for children with SAM, it is plausible that adding this high-quality source of lipids and protein to RUTF may also benefit children with SAM in both immediate and long-term physical and cognitive recovery.

This will be an individually randomized, investigator/outcomes assessors-blinded, controlled clinical trial designed to determine if treatment of severely malnourished Sierra Leonean children 6-59-months of age with an RUTF made with MFGM-containing whey protein/fat concentrate will (1) improve neurodevelopment and (2) reduce a composite of poor SAM outcomes (death, hospitalization, remaining severely malnourished), compared with standard RUTF (S-RUTF). This trial will be conducted at 20 rural sites in Sierra Leone. 1600 children will be randomized 1:1 to receive 2 sachets per day of either MFGM-RUTF or S-RUTF. Children will receive their allocated RUTF and return to clinic fortnightly for repeat anthropometric measurements, illness questions, and to receive more RUTF until they achieve a clinical outcome or for a maximum of 12 weeks, at which point they will undergo Malawi Developmental Assessment Tool (MDAT) testing. Participants will be asked to return to clinic 6 (5-7) months later for MDAT testing, the global z-score from which will be the trial's co-primary outcome. A subset of participants will undergo blood spot and/or stool sample collection at the end of SAM treatment.

Being tested
MFGM-RUTF (milk fat globule membrane ready-to-use therapeutic food), S-RUTF (standard ready-to-use therapeutic food), Amoxicillin, Sulfadoxine (250 mg)/Pyrimethamine (12.5 mg)
Keywords
severe acute malnutrition, severe wasting, kwashiorkor, milk fat globule membrane, neurodevelopment, phospholipids, ganglioside, dairy fat, malawi developmental assessment tool, Sierra Leone, ready-to-use therapeutic food
Medical subject headings
Severe Acute Malnutrition, Cognitive Dysfunction, Kwashiorkor, Cachexia

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • MFGM-RUTF (milk fat globule membrane ready-to-use therapeutic food)Dietary supplement

    MFGM whey protein/fat concentrate powder used in place of skim milk powder in peanut paste-based ready-to-use therapeutic food meeting Codex Alimentarius specifications. There will be 10g of MFGM-containing whey protein/fat concentrate powder per 100g of MFGM-RUTF. Other ingredients and amounts per 100g: 9.5g rice flour, 5g whey permeate, 18.5g palm oil, 31g peanut paste, 22.1g sugar, 2.9g micronutrient mix, 1g fish oil.

  • S-RUTF (standard ready-to-use therapeutic food)Dietary supplement

    Standard peanut paste-based ready-to-use therapeutic food made with skim milk powder meeting Codex Alimentarius specifications. This RUTF is modeled on the most widely used recipe worldwide, containing per 100g: 19.5g skim milk powder, 9.3g palm oil, 7g canola oil, 31.3g peanut paste, 28g sugar, 1g soy flakes, 1g hydrogenated vegetable oil, and 2.9g micronutrient mix.

  • AmoxicillinDrug

    Oral amoxicillin tablets twice per day for 7 days dosed based on weight

  • Sulfadoxine (250 mg)/Pyrimethamine (12.5 mg)Drug

    Malaria chemoprophylaxis, dosed by weight, to be given every month during SAM treatment

Study groups in NCT06869850
Study groupRoleWhat they receive
MFGM-RUTF (Milk fat globule membrane ready-to-use therapeutic food)ExperimentalOne sachet contains 92g of MFGM-RUTF. During SAM treatment, each participant will be given sufficient MFGM-RUTF to consume 2 sachets per day, which will provide approximately 1000 calories, 27g of protein, 63g of fat, and over 1 RDA of micronutrients.
Receives: Dietary Supplement: MFGM-RUTF (milk fat globule membrane ready-to-use therapeutic food); Drug: Amoxicillin; Drug: Sulfadoxine (250 mg)/Pyrimethamine (12.5 mg)
S-RUTF (standard ready-to-use therapeutic food)Active comparatorOne sachet contains 92g of S-RUTF. During SAM treatment, each participant will be given sufficient S-RUTF to consume 2 sachets per day, which will provide approximately 1000 calories, 27g of protein, 60g of fat, and over 1 RDA of micronutrients.
Receives: Dietary Supplement: S-RUTF (standard ready-to-use therapeutic food); Drug: Amoxicillin; Drug: Sulfadoxine (250 mg)/Pyrimethamine (12.5 mg)

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Malawi Developmental Assessment Tool global z-score

    Age-standardized score, -6 to +6, higher scores are better

    Measured: 6 (5-7) months after SAM treatment completion

  2. Composite of poor severe acute malnutrition treatment outcomes

    This composite outcome will include death, hospitalization, and remaining severely malnourished despite 12 weeks of treatment

    Measured: 2-12 weeks of therapeutic feeding

Secondary outcomes (22)
  1. Malawi Developmental Assessment Tool gross motor domain z-score

    Age-standardized score, -6 to +6, higher scores are better

    Measured: 6 (5-7) months after SAM treatment completion

  2. Malawi Developmental Assessment Tool fine motor domain z-score

    Age-standardized score, -6 to +6, higher scores are better

    Measured: 6 (5-7) months after SAM treatment completion

  3. Malawi Developmental Assessment Tool language domain z-score

    Age-standardized score, -6 to +6, higher scores are better

    Measured: 6 (5-7) months after SAM treatment completion

  4. Malawi Developmental Assessment Tool social-emotional domain z-score

    Age-standardized score, -6 to +6, higher scores are better

    Measured: 6 (5-7) months after SAM treatment completion

  5. Remaining severely malnourished at end of SAM treatment

    For MUAC enrollment: MUAC < 11.5 cm For WLZ enrollment: WLZ < -3 For enrollment by both MUAC and WLZ: either remaining in SAM range For nutritional edema enrollment: continued edema

    Measured: 12 weeks of therapeutic feeding

  6. Death during SAM treatment

    As per caregiver/family report

    Measured: 2-12 weeks of therapeutic feeding

  7. Hospitalization during SAM treatment

    Participant determined to require hospitalization. Determination may be made by caregiver/family, government health workers, or may be recommended by trial staff for clinical decompensation.

    Measured: 2-12 weeks of therapeutic feeding

  8. Graduation from SAM treatment

    For MUAC enrollment: MUAC ≥ 12.5cm For WLZ enrollment: WLZ > -2 based on enrollment length For MUAC and WLZ enrollment: may meet either For edema enrollment: resolution of edema, with at least 4 weeks treatment

    Measured: 2-12 weeks of therapeutic feeding

  9. Malawi Developmental Assessment Tool global z-score

    Age-standardized score, -6 to +6, higher scores are better

    Measured: Within 1 month of SAM treatment completion

  10. Malawi Developmental Assessment Tool gross motor domain z-score

    Age-standardized score, -6 to +6, higher scores are better

    Measured: Within 1 month of SAM treatment completion

  11. Malawi Developmental Assessment Tool fine motor domain z-score

    Age-standardized score, -6 to +6, higher scores are better

    Measured: Within 1 month of SAM treatment completion

  12. Malawi Developmental Assessment Tool language domain z-score

    Age-standardized score, -6 to +6, higher scores are better

    Measured: Within 1 month of SAM treatment completion

  13. Malawi Developmental Assessment Tool social-emotional domain z-score

    Age-standardized score, -6 to +6, higher scores are better

    Measured: Within 1 month of SAM treatment completion

  14. Rate of weight change

    g / kg / day

    Measured: Across initial 4 weeks of therapeutic feeding, or 2 weeks if graduate after 2 weeks

  15. Rate of length change

    mm / week

    Measured: Across 2-12 weeks of therapeutic feeding

  16. Rate of mid-upper arm circumference change

    mm / week

    Measured: Across 2-12 weeks of therapeutic feeding

  17. Rate of change in length-for-age z-score across entire follow-up

    Difference in LAZ at final visit and initial visit divided by time months transpired

    Measured: 7-10 months (2-12 weeks of therapeutic feeding, 5-7 months of follow-up thereafter)

  18. Diarrhea incidence during SAM treatment

    Caregiver report of participant diarrhea (>2 loose stools per day) during SAM treatment

    Measured: 2-12 weeks of therapeutic feeding

  19. Fever incidence during SAM treatment

    Caregiver report of participant fever during SAM treatment

    Measured: 2-12 weeks of therapeutic feeding

  20. Plasma DHA status at end of SAM treatment

    Blood spot DHA % total fatty acids in subset of participants at end of therapeutic feeding

    Measured: Collected after 2-12 weeks of therapeutic feeding

  21. Fecal host mRNA transcripts as markers of environmental enteric dysfunction at end of SAM treatment

    CD53, CDX1, HLA-DRA, TNF, S100A8, MUC12, and REG1A

    Measured: Collected after 2-12 weeks of therapeutic feeding

  22. Malawi Developmental Assessment Tool global z-score trajectory

    Change in MDAT global z-score between initial test and final test

    Measured: 6 (5-7) months after SAM treatment completion

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted11 Mar 2025
  2. Study start22 Sep 2025
  3. Primary completion1 Dec 2027 (estimated)
  4. Study completion1 Dec 2027 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Masking
Triple blind
Who is masked
Care provider, Investigator, Outcomes assessor
Enrolment
1,600 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06869850
Sponsor's protocol ID
202503015
Acronym
MEND-SAM
Status last verified
Oct 2026
First submitted
5 Mar 2025
Last updated
23 Oct 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Yes

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