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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

Status: Recruiting
Location: See all (3) locations...
Intervention Type: Dietary supplement, Other
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

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).

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 65
Healthy Volunteers: f
View:

• 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

Locations
Other Locations
Italy
IRCCS Auxologico
RECRUITING
Milan
IRCCS San Raffaele
RECRUITING
Roma
IRCCS Istituto Clinico Humanitas
RECRUITING
Rozzano
Contact Information
Primary
Maria Sole Rossato
ms.rossato@pharmanutra.it
+390507846500
Time Frame
Start Date: 2025-12-11
Estimated Completion Date: 2026-12
Participants
Target number of participants: 144
Treatments
Experimental: Myosave®
Participants receive Myosave® twice daily (two sachets/day) for 24 weeks, in addition to standard GLP-1 RA or dual GIP/GLP-1 RA therapy.
Placebo_comparator: Placebo
Participants receive a matching placebo twice daily for 24 weeks, in addition to standard GLP-1 RA or dual GIP/GLP-1 RA therapy.
Related Therapeutic Areas
Sponsors
Leads: Pharmanutra S.p.a.
Collaborators: Sintesi Research Srl

This content was sourced from clinicaltrials.gov