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.
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
- Conditions the study is for
- Severe Acute Malnutrition, Cognitive Impairment, Kwashiorkor
- 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
- Are there results?
- Not yet: the study is under way
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.
10 sites in 1 country
Sierra Leone10 sites, 10 recruiting
- 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
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 group | Role | What they receive |
|---|---|---|
| MFGM-RUTF (Milk fat globule membrane ready-to-use therapeutic food) | Experimental | One 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 comparator | One 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.
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
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)
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
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
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
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
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
Death during SAM treatment
As per caregiver/family report
Measured: 2-12 weeks of therapeutic feeding
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
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
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
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
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
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
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
Rate of weight change
g / kg / day
Measured: Across initial 4 weeks of therapeutic feeding, or 2 weeks if graduate after 2 weeks
Rate of length change
mm / week
Measured: Across 2-12 weeks of therapeutic feeding
Rate of mid-upper arm circumference change
mm / week
Measured: Across 2-12 weeks of therapeutic feeding
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)
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
Fever incidence during SAM treatment
Caregiver report of participant fever during SAM treatment
Measured: 2-12 weeks of therapeutic feeding
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
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
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.
- First posted11 Mar 2025
- Study start22 Sep 2025
- Primary completion1 Dec 2027 (estimated)
- Study completion1 Dec 2027 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Severe Acute MalnutritionStudies of the same condition, open and under way.
- More trials run by Washington University School of MedicineThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
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)
Sponsor and investigators
- Lead sponsor
- Washington University School of Medicine
- Sponsor type
- University, hospital or other
- Collaborators
- Project Peanut Butter, Ministry of Health and Sanitation, Sierra Leone, Arla Foods, The Danish Dairy Research Foundation, Denmark
- Responsible party
- Sponsor
- Investigators
- Mark J Manary, MD, Principal investigator, Washington University School of MedicineKevin B Stephenson, MD, Principal investigator, Washington University School of MedicineIndi Trehan, MD, MPH, Study director, University of Washington
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
Study at a glance
From the registry record, last updated by the sponsor on 23 Oct 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- MFGM-EnhaNceD RUTF for Children With SAM
- ClinicalTrials.gov ID
- NCT06869850
- Acronym / sponsor ID
- MEND-SAM / 202503015
- Keywords
- severe acute malnutrition, severe wasting, kwashiorkor, milk fat globule membrane, neurodevelopment, phospholipids, ganglioside, dairy fat
- Study type
- Interventional
- Recruitment status
- Recruiting
- Enrolment
- 1,600 participants (estimated)
- Lead sponsor
- Washington University School of MedicineUniversity, hospital or other
- Collaborators
- Project Peanut Butter, Ministry of Health and Sanitation, Sierra Leone, Arla Foods, The Danish Dairy Research Foundation, Denmark
- Study start
- 22 Sep 2025 (actual)
- Primary completion
- 1 Dec 2027 (estimated)
- Study completion
- 1 Dec 2027 (estimated)
- First posted
- 11 Mar 2025 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
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?
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
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.
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Triple blind (care provider, investigator, outcomes assessor)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| MFGM-RUTF (Milk fat globule membrane ready-to-use therapeutic food) | Experimental | Dietary Supplement: MFGM-RUTF (milk fat globule membrane ready-to-use therapeutic food), Drug: Amoxicillin, Drug: Sulfadoxine (250 mg)/Pyrimethamine (12.5 mg)One 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. |
| S-RUTF (standard ready-to-use therapeutic food) | Active comparator | Dietary Supplement: S-RUTF (standard ready-to-use therapeutic food), Drug: Amoxicillin, Drug: Sulfadoxine (250 mg)/Pyrimethamine (12.5 mg)One 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. |
Who may qualify
- Ages
- 6 to 59 months
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Child
Key inclusion criteria (4 listed)
- 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
Key exclusion criteria (5 listed)
- 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
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| MFGM-RUTF (milk fat globule membrane ready-to-use therapeutic food)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. | Dietary supplement | MFGM-RUTF (Milk fat globule membrane ready-to-use therapeutic food) |
| S-RUTF (standard ready-to-use therapeutic food)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. | Dietary supplement | S-RUTF (standard ready-to-use therapeutic food) |
| AmoxicillinOral amoxicillin tablets twice per day for 7 days dosed based on weight | Drug | MFGM-RUTF (Milk fat globule membrane ready-to-use therapeutic food), S-RUTF (standard ready-to-use therapeutic food) |
| Sulfadoxine (250 mg)/Pyrimethamine (12.5 mg)Malaria chemoprophylaxis, dosed by weight, to be given every month during SAM treatment | Drug | MFGM-RUTF (Milk fat globule membrane ready-to-use therapeutic food), S-RUTF (standard ready-to-use therapeutic food) |
Primary outcome
Malawi Developmental Assessment Tool global z-score
Time frame: 6 (5-7) months after SAM treatment completion
Age-standardized score, -6 to +6, higher scores are better
Composite of poor severe acute malnutrition treatment outcomes
Time frame: 2-12 weeks of therapeutic feeding
This composite outcome will include death, hospitalization, and remaining severely malnourished despite 12 weeks of treatment
22 secondary outcomes
Malawi Developmental Assessment Tool gross motor domain z-score
Time frame: 6 (5-7) months after SAM treatment completion
Malawi Developmental Assessment Tool fine motor domain z-score
Time frame: 6 (5-7) months after SAM treatment completion
Malawi Developmental Assessment Tool language domain z-score
Time frame: 6 (5-7) months after SAM treatment completion
Malawi Developmental Assessment Tool social-emotional domain z-score
Time frame: 6 (5-7) months after SAM treatment completion
Remaining severely malnourished at end of SAM treatment
Time frame: 12 weeks of therapeutic feeding
Death during SAM treatment
Time frame: 2-12 weeks of therapeutic feeding
Hospitalization during SAM treatment
Time frame: 2-12 weeks of therapeutic feeding
Graduation from SAM treatment
Time frame: 2-12 weeks of therapeutic feeding
Malawi Developmental Assessment Tool global z-score
Time frame: Within 1 month of SAM treatment completion
Malawi Developmental Assessment Tool gross motor domain z-score
Time frame: Within 1 month of SAM treatment completion
Malawi Developmental Assessment Tool fine motor domain z-score
Time frame: Within 1 month of SAM treatment completion
Malawi Developmental Assessment Tool language domain z-score
Time frame: Within 1 month of SAM treatment completion
Malawi Developmental Assessment Tool social-emotional domain z-score
Time frame: Within 1 month of SAM treatment completion
Rate of weight change
Time frame: Across initial 4 weeks of therapeutic feeding, or 2 weeks if graduate after 2 weeks
Rate of length change
Time frame: Across 2-12 weeks of therapeutic feeding
Rate of mid-upper arm circumference change
Time frame: Across 2-12 weeks of therapeutic feeding
Rate of change in length-for-age z-score across entire follow-up
Time frame: 7-10 months (2-12 weeks of therapeutic feeding, 5-7 months of follow-up thereafter)
Diarrhea incidence during SAM treatment
Time frame: 2-12 weeks of therapeutic feeding
Fever incidence during SAM treatment
Time frame: 2-12 weeks of therapeutic feeding
Plasma DHA status at end of SAM treatment
Time frame: Collected after 2-12 weeks of therapeutic feeding
Fecal host mRNA transcripts as markers of environmental enteric dysfunction at end of SAM treatment
Time frame: Collected after 2-12 weeks of therapeutic feeding
Malawi Developmental Assessment Tool global z-score trajectory
Time frame: 6 (5-7) months after SAM treatment completion
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 23 Oct 2026.
- Individual participant dataSharing planned: Yes
Related trials for Severe Acute Malnutrition
Not yet recruiting
The Relapse to Acute Malnutrition Prevention (RAMP) Trial
Acute Malnutrition in Childhood, Acute Malnutrition, Severe
RecruitingPhase 4
Opportunistic Pneumococcal Immunisation Trial in MALnutrition
Severe Acute Malnutrition in Childhood, Pneumococcal Disease
Recruiting
Increasing the Coverage of Severe Acute Malnutrition (SAM) Treatment in Ethiopia
Acute Malnutrition, Severe, Malnutrition, Child
Active, not recruiting
Choline to Improve Malnutrition and Enhance Cognition
Severe Acute Malnutrition, Cognitive Impairment
Enrolling by invitation
Safety Trial of F-60 Among Children Hospitalized With SAM
Dietary Supplementation, Severe Acute Malnutrition
Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part.
Mark J Manary, MD principal investigator
Washington University School of Medicine
Kevin B Stephenson, MD principal investigator
Washington University School of Medicine
Indi Trehan, MD, MPH study director
University of Washington
10 sites in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
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.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 4 inclusion and 5 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: looking for participants now, as of the sponsor's last update on 23 Oct 2026. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 10 sites in Sierra Leone. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
This study is still under way. Results are not available in the source record yet.
How can a doctor refer a patient or contact the research team?
Contact Mark J Manary, MD (+1 314-454-2341, manarymj@wustl.edu), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Malawi Developmental Assessment Tool global z-score (time frame: 6 (5-7) months after SAM treatment completion). The study lists 2 primary outcomes in all. It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 23 Oct 2026.