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NCT07393360Recruiting

Effect of a Food for Special Medical Purposes on Muscle Mass Preservation During GLP-1 RAs Weight Loss Treatment

Evaluating the Effect of a Food for Special Medical Purposes Containing Essential Amino Acids (EAA), Carnitine, Arginine, and Sucrosomial Minerals on the Preservation of Appendicular Skeletal Muscle Mass (ASMM) During a Weight Loss Program With GLP-1 Receptor Agonists

Source: ClinicalTrials.gov · Last updated 23 Mar 2026

Brief summary (registry, in English)

This study evaluates whether a Food for Special Medical Purposes (FSMP) can help to preserve appendicular skeletal muscle mass (ASMM) in adults undergoing weight loss treatment with GLP-1 receptor agonists or dual GIP/GLP-1 receptor agonists. Participants will receive the FSMP or a matching placebo for 24 weeks while continuing standard GLP-1-based therapy. ASMM will be measured using Bioelectrical Impedance Vector Analysis (BIVA).

Status (registry)
Recruiting
Study type
Interventional
Enrollment
144 (estimated)
First submitted
29 Dec 2025
Start date
11 Dec 2025
Primary completion date
Dec 2026
Lead sponsor
Pharmanutra S.p.a.
Diseases
Obesity
NCT number
NCT07393360

What you commit to

  • Study type: Interventional
  • Planned participants: 144
  • From 11 Dec 2025 to the primary completion date, Dec 2026
  • 3 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Use of food supplements containing aminoacids and/or HMB; patients can be included in the study if they undergo a washout period of at least 15 days

Other illness

  • Type I and Type II diabetes; patients with pre-diabetes and/or metabolic syndrome and assuming Metformin and SGLT-2 inhibitors can be enrolled
  • Hypersensitivity to any of the constituents of the study product

Lab values

  • Reduced kidney function, defined as eGFR \< 60 mL/min/1.73 m², calculated using the CKD-EPI equation (see Appendix 1)

Other

  • Monogenic obesity (Subjects with a known diagnosis of monogenic obesity, including but not limited to pathogenic mutations in LEP, LEPR, MC4R, POMC, PCSK1, or other genes known to cause monogenic forms of early-onset or syndromic obesity)
  • Oncologic patients in active treatments
  • Pregnancy
  • Breastfeeding
  • Use of meal replacements for a diet enriched with aminoacids and/or HMB

Who the study is looking for

  • Age ≥18 years and ≤ 65 years old;
  • BMI ≥ 30 Kg/m2 and ≤45 kg/m2
  • BMI from 27 kg/m2 to 30 Kg/m2 with at least one associated co-morbidity related to overweight \[e.g. dysglycemia (pre-diabetes and/or metabolic syndrome), hypertension, dyslipidemia, obstructive sleep apnea syndrome (OSAS\], or cardiovascular disease\]
  • Starting to use a GLP-1 RAs (liraglutide, semaglutide) or dual GIP and GLP-1 RAs (tirzepatide) for weight reduction; patient can be enrolled if they start the treatment at the time of enrollment or up to 2 weeks
  • Diet composition adjusted to provide 0.9-1.1 g/Kg ideal body weight proteins
  • Signed informed consent

Age in the registry: 18 years to 65 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (3)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
IRCCS Auxologico
Coordinator of this site? Confirm its status
MilanItalyRecruiting
IRCCS San Raffaele
Coordinator of this site? Confirm its status
RomaItalyRecruiting
IRCCS Istituto Clinico Humanitas
Coordinator of this site? Confirm its status
RozzanoItalyRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.