Clinical Trials Directory

Trials / Recruiting

RecruitingNCT06941532

GMP Powdered Substitutes in PKU and TYR

Evaluating the Adherence, Tolerance, Acceptability and Safety of New GMP-based Powdered Protein Substitutes in PKU and TYR: a Case Study Series

Status
Recruiting
Phase
N/A
Study type
Interventional
Enrollment
40 (estimated)
Sponsor
Nutricia UK Ltd · Industry
Sex
All
Age
3 Years
Healthy volunteers
Not accepted

Summary

Four new GMP-based protein substitutes have been developed to support the dietary management of PKU and TYR. These products are powdered protein substitutes, low in phenylalanine and low in phenylalanine and tyrosine respectively, with a mix of glycomacropeptide (GMP), essential and non-essential amino acids, carbohydrates, fibres, fats (including DHA) and micronutrients. The proteins in these new protein substitutes are based on GMP, a peptide isolated from milk during cheese manufacturing and the only known naturally derived protein source low in phenylalanine and tyrosine. The GMP is supplemented with other amino acids which are naturally low or not present in GMP, as well as carbohydrates, fats, fibre and micronutrients. Studies to date have illustrated that PKU patients who replace their regular phenylalanine-free amino acid-based formula with GMP-based foods may have better diet compliance and prefer the taste whilst maintaining metabolic control. This series of case-studies aims to evaluate the gastrointestinal tolerance, acceptability, compliance, and safety of these four GMP based protein substitutes in both adults and children over 3 years. These case studies will last 29 days in total, including a 1-day baseline period followed by a 28-day intervention period. The case studies will be conducted across multiple specialist metabolic centres in the UK. A series of case studies is undertaken due to the rarity of these conditions, the diversity of patient types and the difficulty in recruiting these patients to trials.

Conditions

Interventions

TypeNameDescription
DIETARY_SUPPLEMENTGMP Intervention ProductCondition specific GMP based intervention product

Timeline

Start date
2025-05-20
Primary completion
2026-12-31
Completion
2026-12-31
First posted
2025-04-23
Last updated
2025-12-19

Locations

1 site across 1 country: United Kingdom

Source: ClinicalTrials.gov record NCT06941532. Inclusion in this directory is not an endorsement.