Amino Acid Kinetics of GMP-AA in Healthy Human Volunteers

Sponsor
Birmingham Women's and Children's NHS Foundation Trust (Other)
Overall Status
Active, not recruiting
CT.gov ID
NCT05971563
Collaborator
(none)
20
1
3
10.4
1.9

Study Details

Study Description

Brief Summary

Children with phenylketonuria (PKU) are treated with a special diet supplemented with a synthetic protein based on amino acids. These have a poor taste and are inefficiently used by the body. A different type of synthetic protein, called glycomacropeptide is being tried in PKU. It tastes better than amino acids but it requires the addition of some extra amino acids which may worsen how well it is absorbed compared with traditional amino acid supplements. We will perform a 3-part trial in healthy adult volunteers to compare amino acids vs glycomacropeptide protein with a 'normal protein' (casein) to examine the absorption properties of these proteins. Volunteers will take one dose of each of the protein sources on 3 different days. Blood and urine samples will be collected examining the rate of absorption of amino acids over 5 hours on each study day.

Condition or Disease Intervention/Treatment Phase
  • Dietary Supplement: Casein
  • Dietary Supplement: L-amino acids
  • Dietary Supplement: CGMP-AA
N/A

Detailed Description

In the USA, casein glycomacropeptide (CGMP), a low phenylalanine (Phe) 64-amino acid peptide derived from cheese whey, is widely promoted as a low Phe protein substitute in phenylketonuria (PKU). Protein substitute is composed of non-essential and essential amino acids which replace natural protein in the diet in order to enable normal growth and suppression of blood Phe levels.

It is suggested that CGMP has a slower absorption than usual protein substitute based on amino acids only (amino acids-AA). This compositional change may enhance protein utilization leading to improved blood Phe control. In PKU, any protein substitute that has its absorption closer to the normal 'physiological state' should be advantageous but pure CGMP is lacking in several essential and conditionally essential amino acids (e.g. tyrosine, leucine, tryptophan, histidine). To ensure that CGMP is safe for PKU, it is supplemented with deficient AA (CGMP-AA). Evidence from 'normal' nutritional research suggests that adding AA to natural protein (similar to CGMP-AA), worsens rather than improves efficiency of protein absorption. It is essential to ascertain if CGMP-AA enhances, worsens or has the same absorption when compared with traditional AA substitutes, particularly when prescribing CGMP-AA for children and maternal PKU. The investigators aim to perform a three-part, randomized, controlled, trial in healthy adult volunteers comparing absorption of CGMP-AA (study product 1) vs. AA (study product 2) vs. normal protein (casein) (study product 3). After overnight fasting, healthy volunteers will consume a standard dose of each of the study products. Over the course of 4 hours, plasma AA will be monitored 8 times and this will provide greater insight into the kinetic absorption of CGMP-AA in PKU. The investigators hope these results will add to existing safety and efficacy data about using CGMP-AA in PKU.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
20 participants
Allocation:
Randomized
Intervention Model:
Crossover Assignment
Intervention Model Description:
A three-way, randomized, controlled, open-label, crossover, single-dose clinical trial in healthy adult volunteers.A three-way, randomized, controlled, open-label, crossover, single-dose clinical trial in healthy adult volunteers.
Masking:
None (Open Label)
Primary Purpose:
Other
Official Title:
Amino Acid Kinetics of GMP-AA vs. Phenylalanine-free Amino Acids Compared With Natural Protein in Healthy Adults Volunteers
Actual Study Start Date :
Oct 18, 2022
Anticipated Primary Completion Date :
Aug 31, 2023
Anticipated Study Completion Date :
Aug 31, 2023

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: Casein

Dietary Supplement: Casein
Natural protein

Active Comparator: Glycomacropeptide

Dietary Supplement: CGMP-AA
Glycomacropeptide based protein substitute for Phenylketonuria

Active Comparator: L- amino acids

Dietary Supplement: L-amino acids
Synthetic amino acids based protein substitute for Phenylketonuria

Outcome Measures

Primary Outcome Measures

  1. Total EAA concentrations [240 minutes for each protein]

    To compare the total EAA concentrations after oral ingestion of one dose of three different protein supplements: cGMP-AA vs. AA only vs. casein.

  2. Mean CMAX [240 minutes for each protein]

    Mean CMAX within 240 minutes of ingestion of each of the 3 proteins

  3. AUC of EAA's [240 minutes for each protein]

    AUC of EAA's within 240 minutes of ingestion of each of the 3 proteins

Secondary Outcome Measures

  1. Curve characteristics (Cmax) [240 minutes for each protein]

    Curve characteristics (Cmax) of the following quantities: LNAA; BCAA; Total AA; Tyrosine; Phenylalanine; Urea; Insulin.

  2. Curve characteristics (AUC) [240 minutes for each protein]

    Curve characteristics (AUC) of the following quantities: LNAA; BCAA; Total AA; Tyrosine; Phenylalanine; Urea; Insulin.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 50 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Male and female healthy subjects without PKU;

  • 18 to 50 years of age;

  • Female subjects with a negative urine pregnancy test prior to entry into the study and who are practicing an adequate method of birth control during the study;

  • Good general health status proven by medical history and clinical laboratory values within normal limits or considered not clinically significant by the investigator;

  • Non-smokers or not current smokers;

  • Body mass index (BMI) between 18 and 30 kg/m2 and weight (kg)

  • No existence of disorders or any comorbidity.

  • Willing to follow the study protocol and to take the study products;

  • Able to understand study procedures and sign informed consent.

Exclusion Criteria:
  • History of alcohol or drugs abuse;

  • Smokers;

  • Women who are pregnant, breast feeding, or planning to become pregnant during the course of the study;

  • Received an investigational drug or device within 30 days (or 5 half-lives, whichever is longer) of dosing;

  • Existence of any disorder, food allergy or comorbidity (clinically significant including gastrointestinal, renal, pulmonary, hepatic, cardiovascular and endocrine disorders) - to be decided by investigator from medical history;

  • Current illness or infection that could interfere with the study;

  • Use of laxatives;

  • Use of antibiotics in the last 3 months;

  • Use of medication that could influence protein metabolism (like growth hormone, anabolic steroids, hormone replacement) - to be judged by the investigator;

  • Participation in any clinical trial in the last 3 months;

  • Blood donation within the past 3 months;

  • On a medically prescribed diet;

  • Unable to follow the study protocol or provide consent;

  • Unable to take or tolerate one of the study products.

Contacts and Locations

Locations

Site City State Country Postal Code
1 University Hospitals Birmingham NHS Foundation Trust Birmingham West Midlands United Kingdom B15 2TT

Sponsors and Collaborators

  • Birmingham Women's and Children's NHS Foundation Trust

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Birmingham Women's and Children's NHS Foundation Trust
ClinicalTrials.gov Identifier:
NCT05971563
Other Study ID Numbers:
  • 281421
First Posted:
Aug 2, 2023
Last Update Posted:
Aug 2, 2023
Last Verified:
Jul 1, 2023
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Aug 2, 2023