Could a simple drug tweak metabolism in obesity?
NCT ID NCT05028803
First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study tested whether sodium phenylbutyrate can lower levels of branched chain amino acids (BCAAs) in the blood of obese and prediabetic men. High BCAAs are linked to insulin resistance and type 2 diabetes. Researchers also looked at how the drug affects blood sugar, insulin sensitivity, and muscle protein building. The trial involved 8 men and was completed at the University of Nottingham.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- sodium phenylbutyrate
- What this could lead to
- If successful, this could point toward a way to improve metabolic health in people with obesity or prediabetes by lowering certain amino acids.
- What could go wrong
- This is a very small, early-stage study with only 8 participants, so results may not apply to the general population. The drug may not meaningfully affect blood sugar or insulin sensitivity.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
-
Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
-
8 people
The number who actually took part.
- Started
-
Sep 2021
- Finished
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Mar 2024
- Lead sponsor
-
Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
-
18 to 60 years
- Sex
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Male participants only
- Healthy volunteers
-
Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * • Participant is willing and able to give informed consent for participation in the study * Not currently taking any medications * Males between the ages of 18 - 60 * BMI ≥ 30 kg·m2 * FBG ≥ 6 mmol/L ≤ 7mmol/L or HbA1c ≥ 42 mmol/mol 48 ≤ mmol/mol Exclusion Criteria: * • Specify any diseases/disorders/ conditions that would preclude entry into the study * Females * History or current psychiatric illness * History or current neurological condition (e.g. epilepsy) * Having taken part in a research study in the last 3 months involving invasive procedures or an inconvenience allowance (this must remain for ALL UoN FMHS UREC approved studies) * A BMI \< 30kg·m2 * FBG \>7mmol/L/ or HbA1c \>48mmol/mol * Metabolic disease; Active inflammatory bowel disease * Chronic kidney disease * Malignancy * Recent (6 mo) steroid/ hormone therapy * Clotting dysfunction * Musculoskeletal/ neurological disorders * Active cardiovascular disease or recent cardiac event * Respiratory disease (not including well-controlled asthma)
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
-
University of Nottingham
Derby, Derbyshire, DE22 3NE, United Kingdom
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